Internet-Based Relapse Prevention vs Face to Face Therapy at an Employee Assistance Program (FoBeMA)
Internet-Based Relapse Prevention With Therapist Support vs Face to Face Therapy at an Employee Assistance Program: A Randomized Controlled Non-inferiority Trial
Objectives: This study will evaluate the efficacy of internet-based relapse prevention with therapist support, as compared to face-to-face therapy at an employee assistance program. The design is a two-armed randomized controlled design, and outcomes are measured in terms of changes in problematic alcohol use, as well as depression and quality of life.
Method: Participants with problematic alcohol use who, after an initial evaluation consisting of five face-to-face sessions with a licensed psychologist where alcohol and collateral problems are extensively assessed, are recommended treatment for problematic alcohol use. Consenting participants will be randomized into one of two groups: 1. Internet delivered relapse prevention with therapist support or 2. Face-to-face therapy. Outcomes on alcohol use, depression and quality of life as well as information on user satisfaction will be gathered post treatment. Follow up will be at 3, 6 and 12 months after completion.
Our hypothesis is that the internet-based program with therapist support and the face-to-face therapy will be equally effective in reducing alcohol use (non-inferiority).
研究概览
研究类型
注册 (实际的)
阶段
- 不适用
联系人和位置
学习地点
-
-
-
Stockholm、瑞典、171 76
- Karolinska Institutet, department of clinical neuroscience
-
-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
Problematic alcohol use and having been recommended psychotherapy by the assessing psychologist.
Exclusion Criteria:
Inadequate Swedish language skills No Internet access Reading and/or writing difficulties Major depression Current suicidal thoughts and/or plans Primary problematic drug use PTSD-related problems Psychosis Cognitive disability
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:eChange web-based relapse prevention
A relapse intervention program consisting of 14 modules.
Patients will have access to therapist support through an internal secure messaging system.
|
A web-based relapse intervention program consisting of 14 modules.
The patient will have access to therapist support through a secure messaging system
|
|
有源比较器:Face-to-face therapy
Face-to-face psychotherapy, consisting of 20 sessions.
The content will be vary for different therapists, but all have an evidence-based approach to therapy
|
Face-to-face psychotherapy, consisting of 20 sessions.
The content will be different for different therapists, but all have an evidence based approach to therapy
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Alcohol Use Identification Test (AUDIT)
大体时间:Post, 3, 6 and 12 months
|
Change in total AUDIT score, as a summarized measure of alcohol use (including alcohol consumption and alcohol-related problems)
|
Post, 3, 6 and 12 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Time Line Follow Back (TLFB)
大体时间:Post, 3, 6 and 12 months
|
Change in total TLFB score, as a summarized measure of alcohol consumption
|
Post, 3, 6 and 12 months
|
|
Montgomery Asberg Depression Rating Scale - Self report (MADRS-S)
大体时间:Post, 3, 6 and 12 months
|
Change in total MADRS-S score, as a summarized measure of depression
|
Post, 3, 6 and 12 months
|
|
World Health Quality of Life Scale (WHOQOL-BREF)
大体时间:Post, 3, 6 and 12 months
|
Change in total WHOQOL-BREF score, as a summarized measure of quality of life
|
Post, 3, 6 and 12 months
|
其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Drug Use Identification Test (DUDIT)
大体时间:Post, 3, 6 and 12 months
|
Change in total DUDIT score, as a summarized measure of drug (including alcohol consumption and alcohol-related problems)
|
Post, 3, 6 and 12 months
|
|
Biological tests for alcohol markers
大体时间:Post
|
Biological marker outcomes post-treatment.
B-PEth and CDT.
|
Post
|
合作者和调查者
调查人员
- 首席研究员:Anne H Berman, PhD、Karolinska Institutet
出版物和有用的链接
研究记录日期
研究主要日期
学习开始
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (估计)
研究记录更新
最后更新发布 (估计)
上次提交的符合 QC 标准的更新
最后验证
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.