Feasibility of a Technology-Based Treatment Support System
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 入组人数
- 11
- 试验地点
- 1
- 主要终点
- Retention
研究概览
简要总结
This study aims to evaluate a technology-based treatment support system for patients undergoing the treatment of depression. The investigators will explore the usefulness of the technology-based treatment support system as an adjunct to psychotherapy for depression.
详细描述
This study aims to evaluate a technology-based treatment support system "mConnect" for patients undergoing the treatment of depression. This system will be evaluated by conducting a randomized controlled trial where patients will either receive the mConnect mobile app or treatment as usual.
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
- 否
入选标准
- •18 years of age or older
- •English-speaking
- •Currently enrolled in outpatient treatment
- •Current diagnosis of major depressive disorder
- •Ownership of a smartphone device compatible with the mobile app
排除标准
- •visual, hearing, voice, or motor impairment that would prevent completion of the study procedures or use of mobile phone
- •diagnosis of a psychotic disorder, bipolar disorder, dissociative disorder, substance use disorder, or other diagnosis for which participation in this trial is inappropriate, severe suicidality (has ideation, plan, and intent).
- •having completed more than 3 sessions of psychotherapy with current therapist
研究组 & 干预措施
Mobile App
Participants will receive a mobile app to be used during psychotherapy that syncs information with the participant's therapist from sessions.
干预措施: Mobile App (Behavioral)
Treatment as Usual
Participants will receive treatment as usual with aspects of the mobile app available through paper-based worksheets.
结局指标
主要结局
Retention
时间窗: 8 weeks
Number of completed sessions
Adherence
时间窗: 8 weeks
The use of the mobile app. This data will be collected passively by the mobile app sending the following information to the secure server: the date and time the mobile app is launched, the date and time any information is entered into the mobile app, the content of any information entered into the mobile app, the date and time any lessons within the mobile app are read by the participant.
Satisfaction
时间窗: 8 weeks
Participant satisfaction with the mobile app will be assessed with a patient version of the Mobile App Rating Scale (MARS) that addresses engagement, functionality, aesthestics, information quality, and one subjective rating of the app as a whole.
次要结局
- Depression(8 weeks)
研究者
Stephen Schueller
Assistant Professor of Preventive Medicine
Northwestern University