NCT03500536已完成不适用
Implementing an Innovative Suite of Mobile Applications for Depression and Anxiety
Actualize Therapy2 个研究点 分布在 1 个国家目标入组 146 人开始时间: 2018年7月18日最近更新:
适应症
干预措施
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 146
- 试验地点
- 2
- 主要终点
- Symptoms of depression
研究概览
简要总结
The clinical study is meant to optimize the mobile intervention, to develop a robust implementation plan for the mobile intervention within primary care, and to conduct an effectiveness trial, randomizing 128 participants in order to understand effect on severity of depression and anxiety symptoms, cost-effectiveness, and usability of mobile apps.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- Triple (Participant, Care Provider, Outcomes Assessor)
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
- •Positive screen on PHQ-9
排除标准
- •Does not own or use a mobile smart phone
研究组 & 干预措施
Waitlist Control
No Intervention
8 weeks of treatment as usual followed by 8 weeks of IntelliCare treatment.
Experimental
Experimental
8 weeks of IntelliCare treatment followed by 8 weeks of treatment as usual.
干预措施: IntelliCare (Behavioral)
结局指标
主要结局
Symptoms of depression
时间窗: 8 weeks
Using the PHQ-9 screener
次要结局
未报告次要终点
研究者
Pauli Lieponis
Interim Principal Investigator
Actualize Therapy
研究点 (2)
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