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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02761720
Other study ID # 821784
Secondary ID
Status Completed
Phase N/A
First received May 3, 2016
Last updated May 3, 2016
Start date February 2015

Study information

Verified date May 2016
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 72
Est. completion date
Est. primary completion date November 2015
Accepts healthy volunteers No
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Positive screening for elevated depression symptomatology (PHQ-9 score must be greater than or equal to 5.)

Exclusion Criteria:

- Women with pregnancies of less than 33 weeks gestation.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
No Intervention


Locations

Country Name City State
United States Dickens Center for Women's Health at the Hospital of the University of Pennsylvania Philadelphia Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
University of Pennsylvania Ginger.io

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evidence of increased provider intervention for the treatment of worsening depressive symptoms confirmed by the mobile mood tracking application. 8 weeks No
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