Integrating a Suite of Mental Health Apps for Depression in a Healthcare Setting
1 other identifier
interventional
82
1 country
2
Brief Summary
The purpose of this study is to evaluate the implementation of IntelliCare as a frontline intervention within health care settings.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable depression
Started May 2022
2 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 2, 2022
CompletedFirst Posted
Study publicly available on registry
March 10, 2022
CompletedStudy Start
First participant enrolled
May 1, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
April 30, 2024
CompletedJuly 31, 2024
July 1, 2024
2 years
March 2, 2022
July 30, 2024
Conditions
Outcome Measures
Primary Outcomes (2)
Reach
1\. Number of eligible patients during trial period; 2) number offered IntelliCare; 3) number initiating IntelliCare; 4) number completing IntelliCare
5 months
Cost
Cost of delivering IntelliCare per patient
7 months
Secondary Outcomes (1)
Depression
Administered weekly over 8 weeks
Study Arms (1)
IntelliCare
OTHER8 weeks of IntelliCare
Interventions
A mobile intervention that use principles of computerized therapy to decrease symptoms of depression
Eligibility Criteria
You may qualify if:
- Patient who have been identified as depressed or anxious by a care provider in one of the participating healthcare organizations.
You may not qualify if:
- None
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (2)
Northwestern Medicine Dept of Psychiatry
Chicago, Illinois, 60611, United States
MacLeod HealthCare
Florence, South Carolina, 29506, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Carolyn MacIver
Adaptive Health, Inc
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 2, 2022
First Posted
March 10, 2022
Study Start
May 1, 2022
Primary Completion
April 30, 2024
Study Completion
April 30, 2024
Last Updated
July 31, 2024
Record last verified: 2024-07
Data Sharing
- IPD Sharing
- Will not share