Ignite Creation Date:
2024-05-05 @ 11:56 AM
Last Modification Date:
2024-10-26 @ 9:16 AM
Study NCT ID:
NCT00183365
Status:
COMPLETED
Last Update Posted:
2014-02-07
First Post:
2005-09-12
Brief Title:
Effect of Family-Based Prevention on Children of Depressed Parents
Sponsor:
Childrens Hospital of Philadelphia
Organization:
Childrens Hospital of Philadelphia
Study Overview
Official Title:
Children of Depressed Parents Family-Based Prevention
Status:
COMPLETED
Status Verified Date:
2014-02
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 Protecting Families Program a 10-week prevention program for depressed parents and their pre-teenage children by comparing the effectiveness of the program versus parent training alone
Detailed Description:
Children of depressed parents are at risk for developing social-emotional problems Despite the fact that economic hardship is a strong risk factor for both maternal depression and poor child development little research has been conducted to develop prevention programs for low-income urban families This randomized open-label study will address the research gap by developing and pilot-testing the Protecting Families Program PFP a family-based multi-component prevention program The PFP will offer its services to low-income urban depressed parents and their children between the ages of 9 and 14
Prior to the interventional portion of the study several small focus groups composed of mental-health care providers and depressed parents will meet The purpose of these focus groups will be to gather information that will help maximize the effectiveness of the remainder of the study The interventional phase will compare PFP combined with individual parent training versus parent training alone Participants will be randomly assigned to one of these two intervention groups The study will last a total of 10 weeks Both groups will meet once each week PFP will include a community meal at the beginning of each session a parent skills training group and a concurrent cognitive behavioral therapy CBT group for the focal child Participants symptoms diagnosis functional status family functioning cognitive factors and parenting practices will be assessed at the study start date immediately post-intervention and 6 months post-intervention
Prior to the interventional portion of the study several small focus groups composed of mental-health care providers and depressed parents will meet The purpose of these focus groups will be to gather information that will help maximize the effectiveness of the remainder of the study The interventional phase will compare PFP combined with individual parent training versus parent training alone Participants will be randomly assigned to one of these two intervention groups The study will last a total of 10 weeks Both groups will meet once each week PFP will include a community meal at the beginning of each session a parent skills training group and a concurrent cognitive behavioral therapy CBT group for the focal child Participants symptoms diagnosis functional status family functioning cognitive factors and parenting practices will be assessed at the study start date immediately post-intervention and 6 months post-intervention
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 |
|---|---|---|---|
| DDTR B4-ARD | US NIH GrantContract | None | httpsreporternihgovquickSearchR34MH071868 |
| R34MH071868 | NIH | None | None |