Nancy P Barnett, Matthew K Meisel, Alexander W Sokolovsky, Shannon R Forkus, Kristina M Jackson
Adolescents and young adults often engage in risk behaviors in close proximity to peers. Detecting peer presence could identify high-risk contexts, but typically relies on self-report, which is prone to bias. This study evaluated the feasibility, acceptability, functionality, and validity of a smartphone-based passive detection system using Bluetooth beacons to identify real-world peer proximity. Twenty-one young adult participants (38% women) and their peers (N = 55; 40% women) completed a 3-week protocol, during which peers carried a small Bluetooth beacon that was detected by participant smartphones. Participants indicated the presence of peers on beacon signal-contingent ecological momentary assessment reports and three daily random reports. Feasibility of participant recruitment was low, primarily due to Android OS updates requiring app revisions that interrupted recruitment. However, feasibility of peer enrollment was high, occurring rapidly but at a lower-than-expected number. Response latencies to signal-contingent and random reports were similar, indicating good feasibility of the ecological momentary assessment report procedures. Acceptability, reflected in high retention for participants and peers, participant self-report ratings, and good ecological momentary assessment report response rates (76%-79%), was high. Functionality was moderate; problems with the app were reported by almost half of participants, and functionality ratings were lower than for acceptability. For validity, the beacon detection technology identified 61% of participant-reported encounters (true positives), with 5.6% false positives. False negatives (39%) were likely due to peer noncompliance or misreporting. Results support the initial utility of Bluetooth-based passive detection for identifying peer presence in real time, offering potential for use in just-in-time interventions targeting health-risk behaviors. (PsycInfo Database Record (c) 2026 APA, all rights reserved).
{"title":"The utility of bluetooth and smartphone technology to detect peer contact.","authors":"Nancy P Barnett, Matthew K Meisel, Alexander W Sokolovsky, Shannon R Forkus, Kristina M Jackson","doi":"10.1037/pha0000827","DOIUrl":"10.1037/pha0000827","url":null,"abstract":"<p><p>Adolescents and young adults often engage in risk behaviors in close proximity to peers. Detecting peer presence could identify high-risk contexts, but typically relies on self-report, which is prone to bias. This study evaluated the feasibility, acceptability, functionality, and validity of a smartphone-based passive detection system using Bluetooth beacons to identify real-world peer proximity. Twenty-one young adult participants (38% women) and their peers (<i>N</i> = 55; 40% women) completed a 3-week protocol, during which peers carried a small Bluetooth beacon that was detected by participant smartphones. Participants indicated the presence of peers on beacon signal-contingent ecological momentary assessment reports and three daily random reports. Feasibility of participant recruitment was low, primarily due to Android OS updates requiring app revisions that interrupted recruitment. However, feasibility of peer enrollment was high, occurring rapidly but at a lower-than-expected number. Response latencies to signal-contingent and random reports were similar, indicating good feasibility of the ecological momentary assessment report procedures. Acceptability, reflected in high retention for participants and peers, participant self-report ratings, and good ecological momentary assessment report response rates (76%-79%), was high. Functionality was moderate; problems with the app were reported by almost half of participants, and functionality ratings were lower than for acceptability. For validity, the beacon detection technology identified 61% of participant-reported encounters (true positives), with 5.6% false positives. False negatives (39%) were likely due to peer noncompliance or misreporting. Results support the initial utility of Bluetooth-based passive detection for identifying peer presence in real time, offering potential for use in just-in-time interventions targeting health-risk behaviors. (PsycInfo Database Record (c) 2026 APA, all rights reserved).</p>","PeriodicalId":12089,"journal":{"name":"Experimental and clinical psychopharmacology","volume":" ","pages":""},"PeriodicalIF":2.2,"publicationDate":"2026-02-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146141624","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-11-10DOI: 10.1037/pha0000808
Laura J Holt, Alison Looby, Ty S Schepis, Richard Feinn
Prescription stimulant diversion (PSD) and misuse (PSM) are prevalent among young adults with stimulant prescriptions and have been associated with conduct problems and poorer attention-deficit/hyperactivity disorder symptom management, functional impairment, and other substance use and misuse. Few evidence-based interventions address PSD and PSM; to date, no research has examined for whom these interventions are most/least effective and potential downstream benefits on psychosocial functioning. In the present study, we examined whether conduct problems in childhood moderated response to an interactive web-based intervention focused on preventing PSD and PSM and whether immediate release prescriptions were associated with more PSD and PSM. We also evaluated the impact of the intervention on functional impairment, binge drinking, other substance use, and accidental injuries. We randomized students from three U.S. universities with current stimulant prescriptions (Mage = 20.42 years, 74% female, 86% White) to the intervention (n = 128) or attention-matched placebo (n = 121) in a single-blind design, with 3- and 6-month follow-ups. Conduct problems and being prescribed an immediate release medication were associated with a greater likelihood of PSD, but not PSM; however, conduct problems were not associated with a differential response to the intervention (any PSD/PSM). Compared to the placebo, the intervention group reported lower attention-deficit/hyperactivity disorder impairment and substance use at the 6-month follow-up; rates of accidental injuries did not differ between the two groups. Findings suggest the intervention had significant but modest effects on psychosocial outcomes. Future targeted interventions for PSD may focus on students with conduct problem histories and/or immediate release prescriptions. (PsycInfo Database Record (c) 2026 APA, all rights reserved).
处方兴奋剂转移(PSD)和滥用(PSM)在服用兴奋剂处方的年轻人中很普遍,并与行为问题、注意力缺陷/多动障碍症状管理较差、功能损害和其他物质使用和滥用有关。针对PSD和PSM的循证干预措施很少;迄今为止,还没有研究检查这些干预措施对谁最有效/最无效以及对社会心理功能的潜在下游益处。在本研究中,我们研究了儿童时期的行为问题是否会调节对以预防PSD和PSM为重点的交互式网络干预的反应,以及立即释放处方是否与更多的PSD和PSM相关。我们还评估了干预对功能障碍、酗酒、其他物质使用和意外伤害的影响。在单盲设计中,我们将来自美国三所大学目前服用兴奋剂处方的学生(年龄20.42岁,74%女性,86%白人)随机分为干预组(n = 128)或注意匹配安慰剂组(n = 121),随访3个月和6个月。行为问题和服用立即释放药物与患PSD的可能性增加有关,但与PSM无关;然而,行为问题与干预(任何PSD/PSM)的差异反应无关。与安慰剂组相比,干预组在6个月的随访中报告了更低的注意力缺陷/多动障碍损害和物质使用;意外伤害率在两组之间没有差异。研究结果表明,干预对社会心理结果有显著但适度的影响。未来针对PSD的针对性干预可能会集中在有行为问题史的学生和/或立即释放处方。(PsycInfo Database Record (c) 2025 APA,版权所有)。
{"title":"Preventing prescription stimulant diversion and misuse through brief intervention: Moderators and secondary outcomes from a randomized controlled trial.","authors":"Laura J Holt, Alison Looby, Ty S Schepis, Richard Feinn","doi":"10.1037/pha0000808","DOIUrl":"10.1037/pha0000808","url":null,"abstract":"<p><p>Prescription stimulant diversion (PSD) and misuse (PSM) are prevalent among young adults with stimulant prescriptions and have been associated with conduct problems and poorer attention-deficit/hyperactivity disorder symptom management, functional impairment, and other substance use and misuse. Few evidence-based interventions address PSD and PSM; to date, no research has examined for whom these interventions are most/least effective and potential downstream benefits on psychosocial functioning. In the present study, we examined whether conduct problems in childhood moderated response to an interactive web-based intervention focused on preventing PSD and PSM and whether immediate release prescriptions were associated with more PSD and PSM. We also evaluated the impact of the intervention on functional impairment, binge drinking, other substance use, and accidental injuries. We randomized students from three U.S. universities with current stimulant prescriptions (<i>M</i><sub>age</sub> = 20.42 years, 74% female, 86% White) to the intervention (<i>n</i> = 128) or attention-matched placebo (<i>n</i> = 121) in a single-blind design, with 3- and 6-month follow-ups. Conduct problems and being prescribed an immediate release medication were associated with a greater likelihood of PSD, but not PSM; however, conduct problems were not associated with a differential response to the intervention (any PSD/PSM). Compared to the placebo, the intervention group reported lower attention-deficit/hyperactivity disorder impairment and substance use at the 6-month follow-up; rates of accidental injuries did not differ between the two groups. Findings suggest the intervention had significant but modest effects on psychosocial outcomes. Future targeted interventions for PSD may focus on students with conduct problem histories and/or immediate release prescriptions. (PsycInfo Database Record (c) 2026 APA, all rights reserved).</p>","PeriodicalId":12089,"journal":{"name":"Experimental and clinical psychopharmacology","volume":" ","pages":"61-67"},"PeriodicalIF":2.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145488266","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-04DOI: 10.1037/pha0000809
Brett W Gelino, Julia W Felton, I-Tzu Hung, Justin C Strickland, Geoffrey D Kahn, Nathaniel S Thomas, Joshua L Gowin, Matthew E Sloan, Abraham A Palmer, Sandra Sanchez-Roige, Marcos R Sanches, Sarah W Yip, Brion S Maher, Jill A Rabinowitz
Delay discounting tasks are increasingly used across psychology to examine self-regulation and value-based decision making. These tasks assess how individuals devalue rewards as delays to receipt increase, with responses expected to follow a decreasing pattern. When participants report higher valuation at longer delays-a violation of this expected trend-such responses are often flagged as nonsystematic and, in many cases, excluded from analysis. Although intended to optimize data quality, such exclusions may systematically bias samples and distort downstream inferences. Using data from the Adolescent Brain Cognitive Development study (N = 11,307), we examined whether nonsystematic responding covaried with demographic, cognitive/behavioral, and environmental characteristics. Nearly half of participants exhibited at least one nonsystematic responding violation, with greater likelihood among youth from low-income households, low-resource neighborhoods, and racially minoritized backgrounds. Nonsystematic responding was also associated with lower abstract reasoning and higher positive urgency. Violations disproportionately occurred at the earliest presented task delays, suggesting a possible learning effect. These findings raise concerns that data exclusion criteria may bias behavioral samples and alter conclusions in translational research domains such as addiction science, behavioral pharmacology, and public health. (PsycInfo Database Record (c) 2026 APA, all rights reserved).
延迟折扣任务越来越多地在心理学中用于检查自我调节和基于价值的决策。这些任务评估个体如何随着收到延迟的增加而降低奖励的价值,预期反应会遵循递减的模式。当参与者在较长时间内报告更高的估值时——违反了这一预期趋势——这种反应通常被标记为非系统性的,在许多情况下,被排除在分析之外。虽然是为了优化数据质量,但这样的排除可能会系统性地使样本产生偏差,并扭曲下游推论。使用来自青少年大脑认知发展研究(N = 11,307)的数据,我们检查了非系统反应是否与人口统计学、认知/行为和环境特征共变。近一半的参与者表现出至少一种非系统的反应违规,来自低收入家庭、低资源社区和少数种族背景的年轻人的可能性更大。非系统反应也与较低的抽象推理和较高的积极紧迫性相关。违规行为不成比例地发生在最早出现的任务延迟中,这表明可能存在学习效应。这些发现引起了人们的关注,即数据排除标准可能会使行为样本产生偏差,并改变成瘾科学、行为药理学和公共卫生等转化研究领域的结论。(PsycInfo Database Record (c) 2025 APA,版权所有)。
{"title":"Delay discounting violations vary by adolescent sociodemographics: Excluding nonsystematic data may bias conclusions.","authors":"Brett W Gelino, Julia W Felton, I-Tzu Hung, Justin C Strickland, Geoffrey D Kahn, Nathaniel S Thomas, Joshua L Gowin, Matthew E Sloan, Abraham A Palmer, Sandra Sanchez-Roige, Marcos R Sanches, Sarah W Yip, Brion S Maher, Jill A Rabinowitz","doi":"10.1037/pha0000809","DOIUrl":"10.1037/pha0000809","url":null,"abstract":"<p><p>Delay discounting tasks are increasingly used across psychology to examine self-regulation and value-based decision making. These tasks assess how individuals devalue rewards as delays to receipt increase, with responses expected to follow a decreasing pattern. When participants report higher valuation at longer delays-a violation of this expected trend-such responses are often flagged as nonsystematic and, in many cases, excluded from analysis. Although intended to optimize data quality, such exclusions may systematically bias samples and distort downstream inferences. Using data from the Adolescent Brain Cognitive Development study (<i>N</i> = 11,307), we examined whether nonsystematic responding covaried with demographic, cognitive/behavioral, and environmental characteristics. Nearly half of participants exhibited at least one nonsystematic responding violation, with greater likelihood among youth from low-income households, low-resource neighborhoods, and racially minoritized backgrounds. Nonsystematic responding was also associated with lower abstract reasoning and higher positive urgency. Violations disproportionately occurred at the earliest presented task delays, suggesting a possible learning effect. These findings raise concerns that data exclusion criteria may bias behavioral samples and alter conclusions in translational research domains such as addiction science, behavioral pharmacology, and public health. (PsycInfo Database Record (c) 2026 APA, all rights reserved).</p>","PeriodicalId":12089,"journal":{"name":"Experimental and clinical psychopharmacology","volume":" ","pages":"31-43"},"PeriodicalIF":2.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145676818","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-18DOI: 10.1037/pha0000824
Alison Looby, Katherine A Berry, Anna M Petrey, Emma L Winterlind
Prescription stimulant misuse is prevalent among college students for cognitive, academic, and mood enhancement purposes. While prior research demonstrates placebo effects for subjective mood and drug effects, objective cognitive enhancement placebo effects have been less reliably produced in the laboratory, perhaps because lack of ability to choose to use a drug decreases ecological validity. This study examined whether prescription stimulant placebo effects were modulated by the ability to choose whether to use a drug. College students (N = 183; Mage = 19.48, 92.9% White non-Hispanic, 77.0% female) were randomized into choice (n = 95; ability to choose to ingest 10 mg Adderall [actually placebo]) or no-choice (n = 88; randomly assigned to receive drug [actually placebo] or no drug) conditions before completing subjective effect measures and cognitive tasks. Nearly, all choice participants (n = 90) decided to ingest drug (actually placebo), and were compared against no choice-expect drug (n = 40) and no choice-no drug (n = 48) participants. Replicating prior research, participants who believed they ingested drug indicated subjectively enhanced mood and drug effects on several indices compared to those who did not expect drug; this was not affected by choice. With one exception on a specific reaction time index, there were no placebo effects on objective cognitive tasks, and cognitive performance was similarly not affected by choice. These results provide further evidence of medium-large placebo effects for subjective, but not objective, outcomes following expected prescription stimulant use. Considerations surrounding methodological alterations to laboratory procedures which improve ecological validity are recommended to better understand the influence of both choice and prescription stimulant placebo effects. (PsycInfo Database Record (c) 2026 APA, all rights reserved).
{"title":"To choose or not to choose: Examining the influence of choice on elicitation of subjective and objective prescription stimulant placebo effects in the laboratory.","authors":"Alison Looby, Katherine A Berry, Anna M Petrey, Emma L Winterlind","doi":"10.1037/pha0000824","DOIUrl":"10.1037/pha0000824","url":null,"abstract":"<p><p>Prescription stimulant misuse is prevalent among college students for cognitive, academic, and mood enhancement purposes. While prior research demonstrates placebo effects for subjective mood and drug effects, objective cognitive enhancement placebo effects have been less reliably produced in the laboratory, perhaps because lack of ability to choose to use a drug decreases ecological validity. This study examined whether prescription stimulant placebo effects were modulated by the ability to choose whether to use a drug. College students (<i>N</i> = 183; <i>M</i><sub>age</sub> = 19.48, 92.9% White non-Hispanic, 77.0% female) were randomized into choice (<i>n</i> = 95; ability to choose to ingest 10 mg Adderall [actually placebo]) or no-choice (<i>n</i> = 88; randomly assigned to receive drug [actually placebo] or no drug) conditions before completing subjective effect measures and cognitive tasks. Nearly, all choice participants (<i>n</i> = 90) decided to ingest drug (actually placebo), and were compared against no choice-expect drug (<i>n</i> = 40) and no choice-no drug (<i>n</i> = 48) participants. Replicating prior research, participants who believed they ingested drug indicated subjectively enhanced mood and drug effects on several indices compared to those who did not expect drug; this was not affected by choice. With one exception on a specific reaction time index, there were no placebo effects on objective cognitive tasks, and cognitive performance was similarly not affected by choice. These results provide further evidence of medium-large placebo effects for subjective, but not objective, outcomes following expected prescription stimulant use. Considerations surrounding methodological alterations to laboratory procedures which improve ecological validity are recommended to better understand the influence of both choice and prescription stimulant placebo effects. (PsycInfo Database Record (c) 2026 APA, all rights reserved).</p>","PeriodicalId":12089,"journal":{"name":"Experimental and clinical psychopharmacology","volume":" ","pages":"44-51"},"PeriodicalIF":2.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145774159","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jane P Macky, Kimberly C Kirby, Ben G Fitzpatrick, Shelby Goodwin, Mary Milnamow, Jaime Kishpaugh, Erica J Lubetkin, Michelle L Kuecker, Benjamin Bearnot, Robert J Meyers, Calum J Handley
Community Reinforcement and Family Training (CRAFT) for concerned significant others (CSOs) of individuals with substance use problems (IP) is an efficacious in-person intervention warranting broader dissemination. However, previous web-based delivery studies have not achieved the increases in IP treatment entry seen with in-person studies. We developed two online CRAFT programs closely aligned with the in-person CRAFT protocol and pilot tested their efficacy and feasibility. We block randomized 45 CSOs (15/arm) of IPs with opioid use problems to receive 12 weeks of web-based peer support (PEER) or weekly web-based CRAFT modules with videoconference coaching either in groups (CRAFT-G) or individually (CRAFT-I). Though not statistically significant, more CSOs reported new IP treatment entry in CRAFT-G (76.9%; OR = 5.00, 95% CI [0.03, 3.41], p = .056) and CRAFT-I (72.7%, OR = 4.01, 95% CI [-0.23, 3.20], p = .106) compared to PEER (40.0%), and more CRAFT-G participants reported their IP was in medication treatment at 12 weeks compared to PEER (76.9% vs. 40.0%, OR = 5.00, 95% CI [0.19, 0.98], p = .11). CRAFT-G had significantly improved physical health (p = .025) and mood (p = .015), and both CRAFT-G (p = .018) and CRAFT-I (p = .012) showed increased relationship satisfaction compared to PEER. CSO engagement was similar across conditions. Results must be interpreted cautiously as the study was exploratory and small, and some results were not statistically significant. This pilot study is the first to suggest that online CRAFT programs have the potential to replicate in-person effects, possibly because it did not shorten or significantly alter the in-person protocol when adapting it to a digital format. (PsycInfo Database Record (c) 2026 APA, all rights reserved).
社区加强和家庭培训(CRAFT)是一种有效的面对面干预措施,需要更广泛的传播。然而,以前的基于网络的给药研究并没有达到面对面研究中IP治疗进入率的增加。我们开发了两个与面对面CRAFT协议密切相关的在线CRAFT程序,并对其有效性和可行性进行了试点测试。我们随机分组了45名有阿片类药物使用问题的公民社会组织(15人/组),让他们接受为期12周的基于网络的同伴支持(peer)或每周基于网络的CRAFT模块,并以小组(CRAFT- g)或个人(CRAFT- i)的方式进行视频会议指导。虽然没有统计学意义,但与PEER组(40.0%)相比,CRAFT-G组(76.9%,OR = 5.00, 95% CI [0.03, 3.41], p = 0.056)和CRAFT-I组(72.7%,OR = 4.01, 95% CI [-0.23, 3.20], p = 0.106)有更多的CSOs报告他们的IP在12周时接受药物治疗(76.9%比40.0%,OR = 5.00, 95% CI [0.19, 0.98], p = 0.11)。CRAFT-G显著改善了身体健康(p = 0.025)和情绪(p = 0.015),与PEER相比,CRAFT-G (p = 0.018)和CRAFT-I (p = 0.012)均表现出更高的关系满意度。不同情况下,公民社会组织的参与情况相似。由于本研究为探索性研究,且规模较小,部分结果无统计学意义,因此对结果的解释必须谨慎。这项初步研究首次表明,在线CRAFT项目具有复制现场效果的潜力,可能是因为它在将现场协议调整为数字格式时没有缩短或显著改变现场协议。(PsycInfo数据库记录(c) 2026 APA,版权所有)。
{"title":"Community Reinforcement and Family Training (CRAFT) goes digital: Randomized pilot trial for families of individuals with opioid use problems.","authors":"Jane P Macky, Kimberly C Kirby, Ben G Fitzpatrick, Shelby Goodwin, Mary Milnamow, Jaime Kishpaugh, Erica J Lubetkin, Michelle L Kuecker, Benjamin Bearnot, Robert J Meyers, Calum J Handley","doi":"10.1037/pha0000821","DOIUrl":"10.1037/pha0000821","url":null,"abstract":"<p><p>Community Reinforcement and Family Training (CRAFT) for concerned significant others (CSOs) of individuals with substance use problems (IP) is an efficacious in-person intervention warranting broader dissemination. However, previous web-based delivery studies have not achieved the increases in IP treatment entry seen with in-person studies. We developed two online CRAFT programs closely aligned with the in-person CRAFT protocol and pilot tested their efficacy and feasibility. We block randomized 45 CSOs (15/arm) of IPs with opioid use problems to receive 12 weeks of web-based peer support (PEER) or weekly web-based CRAFT modules with videoconference coaching either in groups (CRAFT-G) or individually (CRAFT-I). Though not statistically significant, more CSOs reported new IP treatment entry in CRAFT-G (76.9%; OR = 5.00, 95% CI [0.03, 3.41], p = .056) and CRAFT-I (72.7%, OR = 4.01, 95% CI [-0.23, 3.20], p = .106) compared to PEER (40.0%), and more CRAFT-G participants reported their IP was in medication treatment at 12 weeks compared to PEER (76.9% vs. 40.0%, OR = 5.00, 95% CI [0.19, 0.98], p = .11). CRAFT-G had significantly improved physical health (p = .025) and mood (p = .015), and both CRAFT-G (p = .018) and CRAFT-I (p = .012) showed increased relationship satisfaction compared to PEER. CSO engagement was similar across conditions. Results must be interpreted cautiously as the study was exploratory and small, and some results were not statistically significant. This pilot study is the first to suggest that online CRAFT programs have the potential to replicate in-person effects, possibly because it did not shorten or significantly alter the in-person protocol when adapting it to a digital format. (PsycInfo Database Record (c) 2026 APA, all rights reserved).</p>","PeriodicalId":12089,"journal":{"name":"Experimental and clinical psychopharmacology","volume":"34 1","pages":"78-87"},"PeriodicalIF":2.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12818555/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145984871","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-09-01DOI: 10.1037/pha0000799
Silvia Murgia, Catharine E Fairbairn, Nancy P Barnett, Julianne Flanagan, Nigel Bosch
Wearable alcohol biosensors offer an innovative solution for real-time alcohol monitoring, yet concerns about comfort, privacy, and social acceptability have limited their adoption. This study presents the largest real-world evaluation to date of a new-generation wrist-worn alcohol biosensor. In this study, 150 healthy adults (ages 21-54) wore the BACtrack Skyn sensor continuously for 14 days. Using a mixed methods design, we assessed pre- and poststudy feasibility and acceptability through structured surveys and open-ended responses, applying innovative machine learning techniques, including Term Frequency-Inverse Document Frequency and sentiment analysis, to capture nuanced user experiences at scale. Participants showed high compliance (median wear time: 94.66%), and 77% expressed willingness to extend device use. The device's discreet, smartwatchlike appearance supported high social acceptability, with most users reporting easy integration into daily life even if no significant changes in alcohol consumption were observed. While some discomfort-particularly itching and sleep interference-was reported, overall comfort and usability ratings were favorable. Findings indicate that the new-generation wrist-worn alcohol biosensor is a feasible and well-accepted tool for alcohol monitoring. High compliance and positive user reception highlight its potential for real-world applications. While sensor comfort was generally positively rated, refining the device's fit and materials could enhance wearability over extended periods. These insights contribute to the ongoing development of wearable alcohol biosensors that balance usability, functionality, and user experience. (PsycInfo Database Record (c) 2026 APA, all rights reserved).
可穿戴酒精生物传感器为实时酒精监测提供了一种创新的解决方案,但对舒适性、隐私性和社会可接受性的担忧限制了它们的采用。这项研究提出了迄今为止对新一代腕戴酒精生物传感器进行的最大的实际评估。在这项研究中,150名健康成年人(21-54岁)连续佩戴BACtrack Skyn传感器14天。使用混合方法设计,我们通过结构化调查和开放式回答评估研究前后的可行性和可接受性,应用创新的机器学习技术,包括术语频率-逆文档频率和情感分析,以大规模捕获细微差别的用户体验。参与者表现出很高的依从性(中位佩戴时间:94.66%),77%的人表示愿意延长设备的使用时间。该设备谨慎的智能手表外观支持高社会接受度,大多数用户表示,即使没有观察到酒精消费量的显着变化,也很容易融入日常生活。虽然有一些不舒服,特别是瘙痒和睡眠干扰,但总体舒适度和可用性评分是有利的。研究结果表明,新一代腕戴式酒精生物传感器是一种可行且被广泛接受的酒精监测工具。高遵从性和积极的用户接受突出了它在实际应用中的潜力。虽然传感器的舒适度普遍得到好评,但改进设备的适配性和材料可以提高长时间的可穿戴性。这些见解有助于可穿戴酒精生物传感器的持续发展,以平衡可用性、功能和用户体验。(PsycInfo Database Record (c) 2025 APA,版权所有)。
{"title":"Acceptability and feasibility of a new-generation alcohol biosensor: A mixed methods evaluation in a large community sample.","authors":"Silvia Murgia, Catharine E Fairbairn, Nancy P Barnett, Julianne Flanagan, Nigel Bosch","doi":"10.1037/pha0000799","DOIUrl":"10.1037/pha0000799","url":null,"abstract":"<p><p>Wearable alcohol biosensors offer an innovative solution for real-time alcohol monitoring, yet concerns about comfort, privacy, and social acceptability have limited their adoption. This study presents the largest real-world evaluation to date of a new-generation wrist-worn alcohol biosensor. In this study, 150 healthy adults (ages 21-54) wore the BACtrack Skyn sensor continuously for 14 days. Using a mixed methods design, we assessed pre- and poststudy feasibility and acceptability through structured surveys and open-ended responses, applying innovative machine learning techniques, including Term Frequency-Inverse Document Frequency and sentiment analysis, to capture nuanced user experiences at scale. Participants showed high compliance (median wear time: 94.66%), and 77% expressed willingness to extend device use. The device's discreet, smartwatchlike appearance supported high social acceptability, with most users reporting easy integration into daily life even if no significant changes in alcohol consumption were observed. While some discomfort-particularly itching and sleep interference-was reported, overall comfort and usability ratings were favorable. Findings indicate that the new-generation wrist-worn alcohol biosensor is a feasible and well-accepted tool for alcohol monitoring. High compliance and positive user reception highlight its potential for real-world applications. While sensor comfort was generally positively rated, refining the device's fit and materials could enhance wearability over extended periods. These insights contribute to the ongoing development of wearable alcohol biosensors that balance usability, functionality, and user experience. (PsycInfo Database Record (c) 2026 APA, all rights reserved).</p>","PeriodicalId":12089,"journal":{"name":"Experimental and clinical psychopharmacology","volume":" ","pages":"18-30"},"PeriodicalIF":2.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144948085","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-12-04DOI: 10.1037/pha0000814
Brian R Katz, Katherine E Menson, Norman Medina, Shannon D O'Connor, David A Kaminsky, Charles G Irvin, Sulamunn R M Coleman, Michael J DeSarno, Stephen T Higgins, Diann E Gaalema
E-cigarettes have been proposed as a harm-reduction strategy to reduce combustible cigarette use. Comparing the cardiopulmonary effects of vaping to smoking is necessary before recommending their use, especially for people at high risk from continued smoking, like those with chronic obstructive pulmonary disease (COPD). Differences in the cardiopulmonary effects of combustible cigarettes and e-cigarettes for people with COPD who smoke were examined. Twenty-one individuals ≥40 years old diagnosed with COPD who smoked (≥5 cigarettes/day for ≥1 year) underwent two consecutive randomly ordered 2-week phases: a cigarette phase (usual-brand cigarettes) and a nicotine-containing e-cigarette phase (combustible cigarette abstinence with 3% and/or 5% nicotine tobacco-flavored JUUL available). Participants earned monetary incentives during the e-cigarette phase for cigarette abstinence, which was biochemically verified with daily carbon monoxide breath testing conducted remotely via phone (readings ≤6 parts per million). Pulmonary (spirometry, oscillometry, COPD Assessment Test, Saint George's Respiratory Questionnaire for COPD) and cardiac (heart rate, blood pressure) measures were completed at baseline, daily (remotely) throughout phases (spirometry, heart rate, and blood pressure only), and after each phase. Changes across assessments were analyzed using mixed-model repeated measures analyses of variance. Diastolic blood pressure and airway resistance at 19 Hz significantly improved during the e-cigarette phase, with the latter restricted to those who substantially abstained from combustible cigarettes (≥10 negative breath carbon monoxide samples) during this phase. The lack of significant adverse cardiopulmonary outcomes following e-cigarette use is promising. However, evaluating longer durations of e-cigarette substitution is warranted to determine their safety as a replacement for combustible cigarettes in patients with COPD. (PsycInfo Database Record (c) 2026 APA, all rights reserved).
电子烟已被提议作为一种减少可燃香烟使用的危害策略。在推荐使用电子烟之前,比较电子烟和吸烟对心肺的影响是必要的,尤其是对于那些持续吸烟的高风险人群,比如那些患有慢性阻塞性肺病(COPD)的人。对吸烟的慢性阻塞性肺病患者的可燃香烟和电子烟的心肺效果进行了研究。21名年龄≥40岁诊断为慢性阻塞性肺病(吸烟≥5支/天,持续≥1年)的患者接受了两个连续随机顺序的2周阶段:香烟阶段(普通品牌香烟)和含尼古丁电子烟阶段(可燃香烟戒断,提供3%和/或5%尼古丁烟草味JUUL)。在电子烟阶段,参与者因戒烟而获得金钱奖励,并通过电话远程进行每日一氧化碳呼吸测试(读数≤百万分之6)进行生化验证。肺(肺活量测定法、振荡测量法、COPD评估试验、COPD的圣乔治呼吸问卷)和心脏(心率、血压)测量在基线、每天(远程)完成整个阶段(肺活量测定法、心率和血压)和每个阶段结束后。使用混合模型重复测量方差分析分析评估间的变化。在电子烟阶段,舒张压和气道阻力在19 Hz下显着改善,后者仅限于在该阶段基本放弃可燃香烟(≥10负呼气一氧化碳样本)的人。电子烟使用后没有显著的不良心肺结果是有希望的。然而,评估更长的电子烟替代持续时间是有必要的,以确定它们作为COPD患者可燃香烟替代品的安全性。(PsycInfo Database Record (c) 2025 APA,版权所有)。
{"title":"Cardiopulmonary effects of combustible cigarettes and e-cigarettes in individuals with chronic obstructive pulmonary disease.","authors":"Brian R Katz, Katherine E Menson, Norman Medina, Shannon D O'Connor, David A Kaminsky, Charles G Irvin, Sulamunn R M Coleman, Michael J DeSarno, Stephen T Higgins, Diann E Gaalema","doi":"10.1037/pha0000814","DOIUrl":"10.1037/pha0000814","url":null,"abstract":"<p><p>E-cigarettes have been proposed as a harm-reduction strategy to reduce combustible cigarette use. Comparing the cardiopulmonary effects of vaping to smoking is necessary before recommending their use, especially for people at high risk from continued smoking, like those with chronic obstructive pulmonary disease (COPD). Differences in the cardiopulmonary effects of combustible cigarettes and e-cigarettes for people with COPD who smoke were examined. Twenty-one individuals ≥40 years old diagnosed with COPD who smoked (≥5 cigarettes/day for ≥1 year) underwent two consecutive randomly ordered 2-week phases: a cigarette phase (usual-brand cigarettes) and a nicotine-containing e-cigarette phase (combustible cigarette abstinence with 3% and/or 5% nicotine tobacco-flavored JUUL available). Participants earned monetary incentives during the e-cigarette phase for cigarette abstinence, which was biochemically verified with daily carbon monoxide breath testing conducted remotely via phone (readings ≤6 parts per million). Pulmonary (spirometry, oscillometry, COPD Assessment Test, Saint George's Respiratory Questionnaire for COPD) and cardiac (heart rate, blood pressure) measures were completed at baseline, daily (remotely) throughout phases (spirometry, heart rate, and blood pressure only), and after each phase. Changes across assessments were analyzed using mixed-model repeated measures analyses of variance. Diastolic blood pressure and airway resistance at 19 Hz significantly improved during the e-cigarette phase, with the latter restricted to those who substantially abstained from combustible cigarettes (≥10 negative breath carbon monoxide samples) during this phase. The lack of significant adverse cardiopulmonary outcomes following e-cigarette use is promising. However, evaluating longer durations of e-cigarette substitution is warranted to determine their safety as a replacement for combustible cigarettes in patients with COPD. (PsycInfo Database Record (c) 2026 APA, all rights reserved).</p>","PeriodicalId":12089,"journal":{"name":"Experimental and clinical psychopharmacology","volume":" ","pages":"88-99"},"PeriodicalIF":2.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12805905/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145676858","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2026-02-01Epub Date: 2025-11-06DOI: 10.1037/pha0000812
John Michael Holden, Cassidy Bos
Sign-tracking, the behavior of approaching and interacting with cues for appetitive outcomes in classical conditioning, has been implicated in relapse to drug addiction. In this experimental study, we examined the serotonin/norepinephrine reuptake inhibitor venlafaxine to determine whether it was effective in reducing sign-tracking in an animal model (Sprague-Dawley male rats, N = 35) of sign-tracking using a retractable lever as a conditioned stimulus and sucrose pellets as an unconditioned stimulus. After training, male rats were administered venlafaxine (0, 30, or 60 mg/kg) intraperitoneally and tested for sign-tracking and goal-tracking (approach of the site of unconditioned stimulus delivery) behaviors. Venlafaxine was significantly effective in reducing sign-tracking in animals previously identified as primarily sign-trackers and intermediates, and it also reduced goal-tracking in animals who primarily goal-tracked. Venlafaxine may be effective in reducing cue-driven approach and interaction behavior that may contribute to relapse in patients rehabilitating from drug use. (PsycInfo Database Record (c) 2026 APA, all rights reserved).
在经典条件反射中,信号追踪是一种接近并与食欲结果线索相互作用的行为,它与药物成瘾的复发有关。在这项实验研究中,我们检测了5 -羟色胺/去甲肾上腺素再摄取抑制剂文拉法辛,以确定它是否有效地减少在动物模型(Sprague-Dawley雄性大鼠,N = 35)中使用可收缩杠杆作为条件刺激和蔗糖颗粒作为非条件刺激的信号跟踪。训练结束后,雄性大鼠腹腔注射文拉法辛(0、30、60 mg/kg),观察其信号跟踪和目标跟踪(非条件刺激传递部位接近)行为。文拉法辛在减少先前确定为主要标志跟踪者和中间物的动物的标志跟踪方面显着有效,并且在主要目标跟踪的动物中也减少了目标跟踪。文拉法辛可能有效地减少线索驱动的方法和相互作用行为,可能有助于患者从药物使用康复复发。(PsycInfo Database Record (c) 2025 APA,版权所有)。
{"title":"Venlafaxine reduces sign-tracking in male Sprague-Dawley rats.","authors":"John Michael Holden, Cassidy Bos","doi":"10.1037/pha0000812","DOIUrl":"10.1037/pha0000812","url":null,"abstract":"<p><p>Sign-tracking, the behavior of approaching and interacting with cues for appetitive outcomes in classical conditioning, has been implicated in relapse to drug addiction. In this experimental study, we examined the serotonin/norepinephrine reuptake inhibitor venlafaxine to determine whether it was effective in reducing sign-tracking in an animal model (Sprague-Dawley male rats, <i>N</i> = 35) of sign-tracking using a retractable lever as a conditioned stimulus and sucrose pellets as an unconditioned stimulus. After training, male rats were administered venlafaxine (0, 30, or 60 mg/kg) intraperitoneally and tested for sign-tracking and goal-tracking (approach of the site of unconditioned stimulus delivery) behaviors. Venlafaxine was significantly effective in reducing sign-tracking in animals previously identified as primarily sign-trackers and intermediates, and it also reduced goal-tracking in animals who primarily goal-tracked. Venlafaxine may be effective in reducing cue-driven approach and interaction behavior that may contribute to relapse in patients rehabilitating from drug use. (PsycInfo Database Record (c) 2026 APA, all rights reserved).</p>","PeriodicalId":12089,"journal":{"name":"Experimental and clinical psychopharmacology","volume":" ","pages":"52-60"},"PeriodicalIF":2.2,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145457809","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Bryan W Jenkins, Cerina Pang, Robbie Y Kuang, Elise M Weerts, Catherine F Moore
Opioid use disorder remains a public health crisis in the United States. A key factor in continued use, relapse risk, and overdose is the severe withdrawal syndrome that accompanies abstinence. Observational studies suggest cannabis may improve outcomes for patients with opioid use disorder and cannabidiol (CBD), a nonintoxicating compound found in cannabis, is being investigated as a potential treatment. This study investigated whether CBD alleviated withdrawal symptoms in a rat model of opioid dependence. Sprague-Dawley rats (N = 100, 50% female) were administered escalating doses of morphine across 10 days (10-50 mg/kg, twice daily). Following abrupt discontinuation, withdrawal outcomes were evaluated across acute (38-hr) and protracted (up to Day 7) timepoints. Rats were treated daily with oral CBD (10 or 30 mg/kg, p.o.) or sesame oil vehicle, beginning 14-hr after their final morphine or saline injection. Withdrawal severity was assessed through physical measurements of body weight, food intake, and somatic signs (e.g., body shakes, diarrhea), pain sensitivity, and measurements of anxiety-like behaviors in the protracted phase. Compared to nondependent controls, morphine-dependent rats had decreased body weight and food intake, showed greater somatic signs, and had increased pain sensitivity that peaked in acute withdrawal (38-hr). In the protracted phase, limited withdrawal signs and no anxiety-like behaviors were detected. Oral CBD did not affect symptoms of opioid withdrawal. These data indicate that CBD alone may have limited effectiveness for treating opioid withdrawal. Reports of improved withdrawal symptoms after cannabis use may be attributed to other compounds in cannabis. (PsycInfo Database Record (c) 2026 APA, all rights reserved).
{"title":"Effects of oral cannabidiol (CBD) on spontaneous opioid withdrawal in male and female rats.","authors":"Bryan W Jenkins, Cerina Pang, Robbie Y Kuang, Elise M Weerts, Catherine F Moore","doi":"10.1037/pha0000826","DOIUrl":"10.1037/pha0000826","url":null,"abstract":"<p><p>Opioid use disorder remains a public health crisis in the United States. A key factor in continued use, relapse risk, and overdose is the severe withdrawal syndrome that accompanies abstinence. Observational studies suggest cannabis may improve outcomes for patients with opioid use disorder and cannabidiol (CBD), a nonintoxicating compound found in cannabis, is being investigated as a potential treatment. This study investigated whether CBD alleviated withdrawal symptoms in a rat model of opioid dependence. Sprague-Dawley rats (<i>N</i> = 100, 50% female) were administered escalating doses of morphine across 10 days (10-50 mg/kg, twice daily). Following abrupt discontinuation, withdrawal outcomes were evaluated across acute (38-hr) and protracted (up to Day 7) timepoints. Rats were treated daily with oral CBD (10 or 30 mg/kg, p.o.) or sesame oil vehicle, beginning 14-hr after their final morphine or saline injection. Withdrawal severity was assessed through physical measurements of body weight, food intake, and somatic signs (e.g., body shakes, diarrhea), pain sensitivity, and measurements of anxiety-like behaviors in the protracted phase. Compared to nondependent controls, morphine-dependent rats had decreased body weight and food intake, showed greater somatic signs, and had increased pain sensitivity that peaked in acute withdrawal (38-hr). In the protracted phase, limited withdrawal signs and no anxiety-like behaviors were detected. Oral CBD did not affect symptoms of opioid withdrawal. These data indicate that CBD alone may have limited effectiveness for treating opioid withdrawal. Reports of improved withdrawal symptoms after cannabis use may be attributed to other compounds in cannabis. (PsycInfo Database Record (c) 2026 APA, all rights reserved).</p>","PeriodicalId":12089,"journal":{"name":"Experimental and clinical psychopharmacology","volume":" ","pages":""},"PeriodicalIF":2.2,"publicationDate":"2026-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145959203","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Michael A Russell, Veronica L Richards, Robert J Turrisi, Yiping Li, Kimberly A Mallett
Day-level alcohol-related problems (ARPs)-such as craving, difficulty limiting/stopping, tolerance, impairment, and withdrawal-may signal risk for alcohol use disorder in young adults' natural settings. ARPs may relate to how people drink (e.g., intensity, speed, duration), but these consumption dynamics are difficult to assess accurately through self-reports. We tested the association between ARPs and alcohol consumption dynamics in young adults using wearable transdermal alcohol concentration (TAC) sensors and daily diaries. College students (N = 79; 55.7% female, 86.1% White, Mage = 20.1) who frequently engaged in heavy episodic drinking wore TAC sensors and completed daily diaries over four consecutive weekends (89.9% completion rate). ARPs were measured the morning after drinking events. Three consumption dynamics were extracted from TAC data: speed (rise rate), intensity (peak), and duration (rise duration) of drinking. Analyses using unadjusted models showed that young adults reported more ARPs on days with faster rise rates, higher peaks, or longer rise durations compared with their own slower, lower, and shorter days. Adjusted models including all three TAC features showed that faster rise rates and longer rise durations were independently associated with ARPs, but higher peaks were not. These findings provide novel evidence that the speed and duration of drinking-not just the amount-may be key targets for ARP prevention among young adults. These insights would not have emerged without the rich, objective measurement of drinking dynamics offered by TAC sensors. TAC features may help indicate existing alcohol-related impairment, warranting investigation of their prospective links to alcohol use disorder risk. (PsycInfo Database Record (c) 2026 APA, all rights reserved).
白天水平的酒精相关问题(ARPs)——如渴望、限制/停止困难、耐受性、损害和戒断——可能是年轻人自然环境中酒精使用障碍风险的信号。arp可能与人们饮酒的方式有关(例如,强度、速度、持续时间),但这些消费动态很难通过自我报告来准确评估。我们使用可穿戴式透皮酒精浓度(TAC)传感器和日常日记测试了年轻人ARPs与酒精消耗动态之间的关系。经常大量饮酒的大学生(N = 79,女性55.7%,白人86.1%,男性20.1)佩戴TAC传感器,并在连续四个周末完成每日日记(完成率89.9%)。在饮酒后的早晨测量arp。从TAC数据中提取三种消费动态:饮酒速度(上升速率)、强度(峰值)和持续时间(上升持续时间)。使用未调整模型的分析显示,与他们自己的较慢、较低和较短的日子相比,年轻人在上升速度较快、峰值较高或上升持续时间较长的日子里报告的arp更多。包括所有三个TAC特征的调整模型显示,更快的上升速率和更长的上升持续时间与ARPs独立相关,但更高的峰值与ARPs无关。这些发现提供了新的证据,证明喝酒的速度和持续时间——而不仅仅是量——可能是年轻人预防ARP的关键目标。如果没有TAC传感器提供的丰富、客观的饮酒动态测量,这些见解就不会出现。TAC特征可能有助于表明现有的酒精相关损伤,因此有必要对其与酒精使用障碍风险的潜在联系进行调查。(PsycInfo Database Record (c) 2025 APA,版权所有)。
{"title":"Alcohol consumption dynamics and day-to-day experiences of alcohol-related problems: Combining transdermal alcohol concentration sensors and daily self-reports in young adults' natural settings.","authors":"Michael A Russell, Veronica L Richards, Robert J Turrisi, Yiping Li, Kimberly A Mallett","doi":"10.1037/pha0000819","DOIUrl":"10.1037/pha0000819","url":null,"abstract":"<p><p>Day-level alcohol-related problems (ARPs)-such as craving, difficulty limiting/stopping, tolerance, impairment, and withdrawal-may signal risk for alcohol use disorder in young adults' natural settings. ARPs may relate to how people drink (e.g., intensity, speed, duration), but these consumption dynamics are difficult to assess accurately through self-reports. We tested the association between ARPs and alcohol consumption dynamics in young adults using wearable transdermal alcohol concentration (TAC) sensors and daily diaries. College students (<i>N</i> = 79; 55.7% female, 86.1% White, <i>M</i><sub>age</sub> = 20.1) who frequently engaged in heavy episodic drinking wore TAC sensors and completed daily diaries over four consecutive weekends (89.9% completion rate). ARPs were measured the morning after drinking events. Three consumption dynamics were extracted from TAC data: speed (rise rate), intensity (peak), and duration (rise duration) of drinking. Analyses using unadjusted models showed that young adults reported more ARPs on days with faster rise rates, higher peaks, or longer rise durations compared with their own slower, lower, and shorter days. Adjusted models including all three TAC features showed that faster rise rates and longer rise durations were independently associated with ARPs, but higher peaks were not. These findings provide novel evidence that the speed and duration of drinking-not just the amount-may be key targets for ARP prevention among young adults. These insights would not have emerged without the rich, objective measurement of drinking dynamics offered by TAC sensors. TAC features may help indicate existing alcohol-related impairment, warranting investigation of their prospective links to alcohol use disorder risk. (PsycInfo Database Record (c) 2026 APA, all rights reserved).</p>","PeriodicalId":12089,"journal":{"name":"Experimental and clinical psychopharmacology","volume":" ","pages":""},"PeriodicalIF":2.2,"publicationDate":"2025-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12716371/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145773996","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}