Social Media Intervention for Postpartum Depression
Completed · Not applicable
Conditions studied: Postpartum Depression, Parenting
In brief
This study is intended to compare the acceptability and feasibility and explore outcomes related to two different formats of a parenting program for mothers with postpartum depressive symptoms. One version will be a traditional, in-person group format, while the other will be a social media group format. The investigators will also explore the differences in outcomes of both formats, looking at depressive symptoms, parenting sense of competency, and parenting interactions with children.
Key facts
- Study ID
- NCT02355067
- Run by
- Children's Hospital of Philadelphia
- People needed
- 40
- Starts
- 2015-01-01
- Expected to finish
- 2017-11-03
- Last updated by the study team
- 2021-03-09
Who can join
Age: 15 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Females
- 15 years of age or older at the start of the study
- English speaking
- Access to the internet via a computer or a smartphone
- Mother of a child 1-3 months old
- Edinburgh Postnatal Depression Scale (EPDS) score of 9 or higher
- Informed consent and HIPAA authorization.
You may not qualify if…
- Have significant suicidal symptoms. Significant suicide risk is defined as current suicidal intent and a plan for suicidal behavior.
Where it is running
- The Children's Hospital of Philadelphia — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.