Ignite Creation Date:
2024-05-05 @ 11:32 AM
Last Modification Date:
2024-10-26 @ 9:09 AM
Study NCT ID:
NCT00074789
Status:
COMPLETED
Last Update Posted:
2013-06-21
First Post:
2003-12-19
Brief Title:
Reducing Symptoms of Depression in Low-Income Mothers
Sponsor:
University of North Carolina Chapel Hill
Organization:
University of North Carolina Chapel Hill
Study Overview
Official Title:
Reducing Depressive Symptoms in Low-Income Mothers
Status:
COMPLETED
Status Verified Date:
2013-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study will test the effectiveness of a short-term intervention in treating depressed young mothers with young children enrolled in Early Head Start Programs
Detailed Description:
Limited resources poor social support and complex life problems contribute to the high prevalence and severity of depressive symptoms in low-income mothers As depressive symptoms persist they often rob young mothers of the energy they need for school job training and positive interaction with their children which can negatively affect a childs language acquisition intellectual development and social conduct This study will design and implement a home-based treatment to help young mothers manage their depressive symptoms increase their social support manage or resolve life issues and effectively parent their infant or toddler through the use of EHS resources
Mothers will be randomly assigned to receive either home-based interpersonal depression treatment or an attention controlusual care condition for 26 weeks Assessments will be made at study start and Weeks 14 22 and 26 Depression scales interviews and analyses of videotaped mother-child interactions will be used to assess participants Stress social support and use of EHS services will be assessed
Mothers will be randomly assigned to receive either home-based interpersonal depression treatment or an attention controlusual care condition for 26 weeks Assessments will be made at study start and Weeks 14 22 and 26 Depression scales interviews and analyses of videotaped mother-child interactions will be used to assess participants Stress social support and use of EHS services will be assessed
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| HILDA | US NIH GrantContract | None | httpsreporternihgovquickSearchR01MH065524 |
| R01MH065524 | NIH | None | None |
| DSIR 83-ATAS | None | None | None |