Development of a Personalized Feedback Intervention Targeting Pain-Related Anxiety for Adults Reporting Hazardous Drinking and Chronic Pain: A Randomized Controlled Trial.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-04-15 DOI:10.15288/jsad.23-00359
Andrew H. Rogers, Clayton Neighbors, Jaye L. Derrick, M. Zvolensky
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Abstract

OBJECTIVE Among individuals with chronic pain, the rate of hazardous alcohol use is elevated compared to the general population. Yet, hazardous drinkers with chronic pain remain an underserved group. There is a need to develop and test alternative and complementary interventions to reduce hazardous alcohol use among this high-risk segment of the general population; targeting pain-related anxiety, a candidate mechanism, is one theoretically-informed route. METHOD Our approach followed a staged model (1a/1b) to develop and test a novel personalized feedback intervention (PFI). Phase 1A collected qualitative feedback from (N = 9; 77.8% female, Mage = 33.86, SD = 8.75) participants to refine intervention content and evaluate treatment acceptability and feasibility. For phase 1B, individuals (N=118; 57.3% male, Mage = 35.24, SD = 11.90) participated in a pilot randomized clinical trial for our novel PFI compared to a health information control condition on alcohol use, intention/motivation to reduce drinking, pain-related anxiety, and expectancies for alcohol analgesia/pain coping for hazardous drinkers with chronic pain. RESULTS Phase 1a results provided support for the feasibility of using a PFI to target pain-related anxiety, and results from Phase 1b indicated that participants reduced drinking and primary outcomes changed in the expected directions, but there were no differential effects of the intervention. CONCLUSIONS The current data provide preliminary evidence for the utility of computer-based brief interventions to encourage behavior change. However, further refinement of the intervention to target pain-related anxiety is warranted.
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针对报告危险饮酒和慢性疼痛的成年人开发与疼痛相关的焦虑的个性化反馈干预:随机对照试验。
目的在慢性疼痛患者中,危险饮酒率高于普通人群。然而,患有慢性疼痛的危险饮酒者仍然是一个服务不足的群体。我们需要开发和测试替代性和补充性干预措施,以减少这一高风险人群中的危险饮酒行为;针对疼痛相关焦虑这一候选机制,是一条具有理论依据的途径。方法我们采用分阶段模式(1a/1b)开发和测试新型个性化反馈干预措施(PFI)。第 1A 阶段收集了参与者(人数 = 9;77.8% 为女性,年龄 = 33.86,标准差 = 8.75)的定性反馈,以完善干预内容并评估治疗的可接受性和可行性。在第 1B 阶段,参与者(人数=118;57.3% 为男性,年龄=35.24,标准差=11.90)参加了一项试验性随机临床试验,与健康信息对照条件相比,我们的新型 PFI 对慢性疼痛危险饮酒者的酒精使用、减少饮酒的意向/动机、疼痛相关焦虑以及对酒精镇痛/疼痛应对的期望进行了比较。结果第一阶段 a 的结果支持使用 PFI 针对疼痛相关焦虑的可行性,第一阶段 b 的结果表明参与者减少了饮酒,主要结果朝着预期的方向发生了变化,但干预没有产生不同的效果。然而,针对疼痛相关焦虑的干预还需要进一步改进。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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