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临床试验/NCT05086172
NCT05086172已完成不适用

Ultrabrief Behavioral Activation for Reducing Alcohol Use

University of North Carolina, Chapel Hill2 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2022年3月8日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
40
试验地点
2
主要终点
Acceptability via summary scores and statistics of study-designed treatment engagement and acceptability assessment instruments

研究概览

简要总结

This is a pilot study to assess feasibility, acceptability, and preliminary efficacy of a single-session ("ultrabrief") psychological intervention to reduce alcohol use in participants with mild to moderate alcohol use disorder (AUD). The intervention is a condensed form of the Life Enhancement Treatment for Substance Use (LETS ACT), behavioral activation (BA) for co-morbid depression and substance use. The investigators hypothesize that UBA is feasible and acceptable. The investigators hypothesize that UBA will reduce overall total alcohol consumption as determined by self-report measures capturing drinking behavior for the 3 months prior to treatment versus the 3 months after treatment when compared to an "assessment only" condition.

详细描述

This is a pilot study to investigate feasibility, acceptability, and preliminary efficacy of an ultrabrief behavioral activation (UBA) intervention for people with a mild to moderate alcohol use disorder. UBA is a psychotherapy intervention derived from the evidence-based LETS ACT BA treatment for substance use disorder. All clinical interviews and the UBA intervention itself will be audio recorded for the purposes of training and to determine reliability and adherence to diagnostic and treatment protocols. No biological samples or signals are collected in this study. The study comprises a phone screening for eligibility, three in-person study visits (initial baseline assessment (BL), UBA intervention session, and 2-week post-treatment assessment) and two follow up phone call assessments (1 month and 3 months after treatment completion). There will be an "assessment only" study arm that will act as a control group which mirrors all aspects of the intervention arm except the "assessment only" arm will receive no intervention. The ultrabrief behavior activation (UBA) intervention is a condensed version of the LETS ACT intervention. The main treatment elements include: (1) explanation of treatment rationale to facilitate behavior change via increased engagement in values-related activities, (2) identification of participant-specific values via detailed assessment of life areas, values and activities, (3) values-based activity planning and scheduling, and (4) post-treatment planning. The overall goal of BA is to shift from values-incongruent behavior (including alcohol use) to behaviors that provide positive reinforcement and environmental reward with the overall goal of increasing the number of engaged-in, value-based activities. This intervention will take 90 minutes. Following intervention completion, therapists will complete a therapist questionnaire and participants will schedule follow-up assessments to occur 2-weeks, 1-month, and 3-months post-treatment. There will be three follow-up contacts with study participants, one in-person visit occurring 2 weeks after the UBA intervention and two phone-based assessments occurring 1 and 3 months following treatment respectively. Follow-up 1 focuses on the treatment experience whereas Follow-up 2 and 3 focus on change in alcohol use and related behaviors and psychological symptoms.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Diagnosis of mild or moderate alcohol use disorder based on Diagnostic and Statistical Manual-V (DSM-5) criteria
  • Age: 18 years or older

排除标准

  • Psychotic disorder as determined by the Mini-International Neuropsychiatric Interview (MINI)
  • Current suicidality as determined by the Columbia Suicide Severity Rating Scale (C-SSRS)
  • Diagnosis of severe alcohol or substance use disorder (AUD;SUD) based on MINI
  • Receiving concurrent psychotherapy for a mental health-related condition
  • Concurrent use of FDA approved medications for the treatment of a substance us disorder
  • Change in psychiatric medication in the last four weeks
  • The inability to give informed, voluntary, written consent to participate
  • Inability to communicate effectively in English as determined by interaction with study personnel
  • Anything else that in the assessment of the investigational team is not conducive to successful completion of study requirements

结局指标

主要结局

Acceptability via summary scores and statistics of study-designed treatment engagement and acceptability assessment instruments

时间窗: 2 weeks Post Treatment (2 week follow-up)

Acceptability will be characterized by computing summary scores and their corresponding statistics from the Treatment Engagement and Acceptability Assessment (TEA) designed for this study. Scores on the TEA range from a minimum score of 20 to a maximum score of 100, with higher scores indicating greater treatment engagement and acceptability.

Feasibility via average rate of enrollment of eligible participants

时间窗: Through completion of the study, an average of 1 year

The investigators will compute the average rate of enrollment of eligible participants when 20 participants have concluded study participation to determine the feasibility of such interventions.

Feasibility via computed fraction of participants who have completed all assessment in this study

时间窗: Baseline up to 3-months Post treatment (Follow up 3)

The investigators will compute the fraction of participants who have completed all assessments in this study (baseline, 2-weeks post treatment, 1-month post treatment-3-months post treatment)

次要结局

  • Feasibility via the therapist questionnaire (TQ) developed by the investigators for this study(Immediately following Treatment Session)
  • Change in alcohol consumption via average amount of alcohol consumed per drinking day(3 months prior to Baseline up to 3-months post treatment)
  • Change in alcohol consumption via number of drinking days(3 months prior to Baseline up to 3-months post treatment)
  • Feasibility via computed fraction of participants that successfully completed at least 1 of each activity independently as per record in treatment booklet(2 weeks Post treatment)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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