NCT03500536CompletedNot Applicable
Implementing an Innovative Suite of Mobile Applications for Depression and Anxiety
Actualize Therapy2 sites in 1 country146 target enrollmentStarted: July 18, 2018Last updated:
Conditions
Interventions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 146
- Locations
- 2
- Primary Endpoint
- Symptoms of depression
Study Overview
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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Supportive Care
- Masking
- Triple (Participant, Care Provider, Outcomes Assessor)
Eligibility Criteria
- Ages
- 18 Years to — (Adult, Older Adult)
- Sex
- All
- Accepts Healthy Volunteers
- Yes
Inclusion Criteria
- •Positive screen on PHQ-9
Exclusion Criteria
- •Does not own or use a mobile smart phone
Arms & Interventions
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.
Intervention: IntelliCare (Behavioral)
Outcomes
Primary Outcomes
Symptoms of depression
Time Frame: 8 weeks
Using the PHQ-9 screener
Secondary Outcomes
No secondary outcomes reported
Investigators
Pauli Lieponis
Interim Principal Investigator
Actualize Therapy
Study Sites (2)
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