Research on Anxiety and Depression: Computer-Assisted Therapy
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 136
- 试验地点
- 2
- 主要终点
- Depression and Anxiety Composite Score
研究概览
简要总结
This study examines how online self-guided programs can improve mood and anxiety symptoms. These programs use exercises from Cognitive-Behavioral Therapy, which is an evidence-based treatment for depression and anxiety. The purpose of this study is to learn who will do best with the online format. Our aim is to learn for whom online self-guided interventions are most efficacious. This knowledge is important because it will help inform clinicians and patients about who might benefit from this type of intervention versus who would need the assistance of a therapist. More specifically, we hope to figure out who would benefit from solely an online intervention and who would benefit from an online intervention in addition to other treatment.
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
- 是
入选标准
- •Previous participation in the RAD study in our laboratory
- •RAD study inclusion criteria are:
- •18+ years of age
- •Fluent and literate in English
- •Can provide informed consent
- •fMRI scanning eligibility, including no evidence of any form of metal embedded in the body (e.g., metal wires, nuts, bolts, screws, plates, sutures)
排除标准
- •Anyone who has not already completed the RAD study will be excluded.
- •RAD study exclusion criteria are:
- •Presence of suicidal ideations representing imminent risk
- •General medical condition, disease, or neurological disorder that interferes with the assessments
- •Mild traumatic brain injury (history of physical brain injury or blow to the head resulting in loss of consciousness greater than five minutes) and which could interfere with doing the assessments
- •Severe impediment to vision, hearing and/or hand movement, likely to interfere with ability to complete the assessments
- •Unable and/or unlikely to follow the study protocols
- •Pregnant or breastfeeding
研究组 & 干预措施
Online Intervention
Participants randomized to the online intervention arm will be given access to the Good Days Ahead program for 12 weeks.
干预措施: Good Days Ahead (Behavioral)
Waitlist
Participants randomized to the waitlist arm will wait for 12 weeks without doing an online intervention.
结局指标
主要结局
Depression and Anxiety Composite Score
时间窗: 12 weeks
Composite score combining 3 measures of depression and/or anxiety (PHQ-9, BAI, DASS)
次要结局
- Quality of Life(12 weeks)
研究者
Tali Manber Ball, PhD
Postdoctoral Scholar
Stanford University