Mobile App for Mood in Pregnancy (Ginger iO)
Completed
- Conditions
- DepressionMood Disorders
- Interventions
- Other: No Intervention
- Registration Number
- NCT02761720
- Lead Sponsor
- University of Pennsylvania
- Brief Summary
The Mobile Mood Tracking App study is a small randomized trial of acceptability and usability of a mobile phone mood tracking application (mobile app) among women with depressed mood in pregnancy. The study will be assessing the perceived value and usability of this tool in pregnancy over eight weeks to test whether women using this app are more likely to receive assessments and treatments of depressed mood than women not using it.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 72
Inclusion Criteria
- Positive screening for elevated depression symptomatology (PHQ-9 score must be greater than or equal to 5.)
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Exclusion Criteria
- Women with pregnancies of less than 33 weeks gestation.
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Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description MPM and Ginger iO No Intervention Participants assigned to this arm downloaded both the MyPennMedicine mobile app and Ginger iO mood tracking app. MyPennMedicine (MPM) No Intervention Participants assigned to this arm downloaded only the MyPennMedicine mobile app. Lottery No Intervention Participants assigned to this arm downloaded both the MyPennMedicine mobile app and Ginger iO mood tracking app. They were also given a lottery incentive if they completed 70% of the daily mood ratings.
- Primary Outcome Measures
Name Time Method Evidence of increased provider intervention for the treatment of worsening depressive symptoms confirmed by the mobile mood tracking application. 8 weeks
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Dickens Center for Women's Health at the Hospital of the University of Pennsylvania
🇺🇸Philadelphia, Pennsylvania, United States