Understanding the Efficacy of Mobile Apps as Intervention for Depression in Adults When Deployed as Part of Primary Care.
Not Applicable
Completed
- Conditions
- DepressionPrimary Health CareAnxiety
- Interventions
- Behavioral: IntelliCare
- Registration Number
- NCT03500536
- Lead Sponsor
- Actualize Therapy
- Brief Summary
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.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 146
Inclusion Criteria
- Positive screen on PHQ-9
Exclusion Criteria
- Does not own or use a mobile smart phone
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Experimental IntelliCare 8 weeks of IntelliCare treatment followed by 8 weeks of treatment as usual.
- Primary Outcome Measures
Name Time Method Symptoms of depression 8 weeks Using the PHQ-9 screener
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of Arkansas for Medical Sciences
🇺🇸Little Rock, Arkansas, United States