接受与承诺疗法在早期精神病患者日常生活中的参与度和可接受性:多中心随机对照试验的二次研究结果。

IF 2 Q3 HEALTH CARE SCIENCES & SERVICES JMIR Formative Research Pub Date : 2024-11-21 DOI:10.2196/57109
Evelyne van Aubel, Thomas Vaessen, Lotte Uyttebroek, Henrietta Steinhart, Annelie Beijer-Klippel, Tim Batink, Ruud van Winkel, Lieuwe de Haan, Mark van der Gaag, Thérèse van Amelsvoort, Machteld Marcelis, Frederike Schirmbeck, Ulrich Reininghaus, Inez Myin-Germeys
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引用次数: 0

摘要

背景:接受与承诺疗法(ACT)在治疗早期精神病方面很有前景。用移动健康生态瞬间干预来增强面对面的 ACT 可能会提高其治疗效果,并使患者有能力将治疗掌握在自己手中:本研究旨在调查和预测日常生活中的接受与承诺疗法(ACT-DL)的治疗参与度和可接受性:在这项多中心随机对照试验中,148 名年龄在 15-65 岁之间的超高危患者或首次发病的精神病患者被随机分配到仅接受常规治疗(对照组)或接受日常生活中的接纳与承诺疗法(ACT-DL)与常规治疗相结合的干预组(实验组),干预组包括 8 次面对面的治疗,并使用基于接纳与承诺疗法的智能手机应用程序,在日常生活中传授接纳与承诺疗法的技能和技巧。对于干预组的患者,我们收集了他们在干预期间和干预后对 ACT-DL 的治疗参与度和接受度的数据。治疗参与度和接受度的预测因素包括基线人口统计学、临床和功能结果:结果:除了接受常规治疗外,接受 ACT-DL 的参与者(人数=71)平均完成了 6 次(标准差 3)疗程,其中 59% 的参与者(人数=42)完成了所有疗程。应用程序参与数据(n=58)显示,参与者每周使用应用程序 13 次,24 次通知中有 6 次(25%)符合要求。汇报得分分布图(人数=46)显示,85%-96%的参与者至少在一定程度上报告了所有可接受性项目的有用性(得分≥2;1=无用性),91%(人数=42)的参与者报告了通知数量和时间长度带来的负担(得分≥2;1=无负担)。多元线性回归模型用于预测治疗参与度和可接受性。少数民族背景预示着较低的通知响应依从性(B=-4.37;P=.01),但较高的应用程序有用性(B=1.25;P=.049)。阴性症状(B=-0.26;P=.01)和情感症状(B=0.14;P=.04)的严重程度分别预示着较低和较高的 ACT 培训有用性。女性(B=-1.03;P=.005)预示着应用程序上的ACT隐喻图像的有用性较低:我们的研究结果证实了早期精神病患者对 ACT-DL 的良好治疗参与度和接受度。我们为未来的干预优化提供了建议:OMON NL46439.068.13; https://onderzoekmetmensen.nl/en/trial/24803.
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Engagement and Acceptability of Acceptance and Commitment Therapy in Daily Life in Early Psychosis: Secondary Findings From a Multicenter Randomized Controlled Trial.

Background: Acceptance and commitment therapy (ACT) is promising in the treatment of early psychosis. Augmenting face-to-face ACT with mobile health ecological momentary interventions may increase its treatment effects and empower clients to take treatment into their own hands.

Objective: This study aimed to investigate and predict treatment engagement with and acceptability of acceptance and commitment therapy in daily life (ACT-DL), a novel ecological momentary intervention for people with an ultrahigh risk state and a first episode of psychosis.

Methods: In the multicenter randomized controlled trial, 148 individuals with ultrahigh risk or first-episode psychosis aged 15-65 years were randomized to treatment as usual only (control) or to ACT-DL combined with treatment as usual (experimental), consisting of 8 face-to-face sessions augmented with an ACT-based smartphone app, delivering ACT skills and techniques in daily life. For individuals in the intervention arm, we collected data on treatment engagement with and acceptability of ACT-DL during and after the intervention. Predictors of treatment engagement and acceptability included baseline demographic, clinical, and functional outcomes.

Results: Participants who received ACT-DL in addition to treatment as usual (n=71) completed a mean of 6 (SD 3) sessions, with 59% (n=42) of participants completing all sessions. App engagement data (n=58) shows that, on a weekly basis, participants used the app 13 times and were compliant with 6 of 24 (25%) notifications. Distribution plots of debriefing scores (n=46) show that 85%-96% of participants reported usefulness on all acceptability items to at least some extent (scores ≥2; 1=no usefulness) and that 91% (n=42) of participants reported perceived burden by number and length of notifications (scores ≥2; 1=no burden). Multiple linear regression models were fitted to predict treatment engagement and acceptability. Ethnic minority backgrounds predicted lower notification response compliance (B=-4.37; P=.01), yet higher app usefulness (B=1.25; P=.049). Negative (B=-0.26; P=.01) and affective (B=0.14; P=.04) symptom severity predicted lower and higher ACT training usefulness, respectively. Being female (B=-1.03; P=.005) predicted lower usefulness of the ACT metaphor images on the app.

Conclusions: Our results corroborate good treatment engagement with and acceptability of ACT-DL in early psychosis. We provide recommendations for future intervention optimization.

Trial registration: OMON NL46439.068.13; https://onderzoekmetmensen.nl/en/trial/24803.

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来源期刊
JMIR Formative Research
JMIR Formative Research Medicine-Medicine (miscellaneous)
CiteScore
2.70
自引率
9.10%
发文量
579
审稿时长
12 weeks
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