Ignite Creation Date:
2024-05-05 @ 6:38 PM
Last Modification Date:
2024-10-26 @ 9:35 AM
Study NCT ID:
NCT00518830
Status:
COMPLETED
Last Update Posted:
2007-08-21
First Post:
2007-08-20
Brief Title:
Treatment of Postnatal Depression for Low-Income Mothers in Primary Care in Santiago Chile
Sponsor:
Fondo Nacional de Desarrollo Científico y Tecnológico Chile
Organization:
Fondo Nacional de Desarrollo Científico y Tecnológico Chile
Study Overview
Official Title:
Randomized Clinical Trial for the Treatment of Postnatal Depression
Status:
COMPLETED
Status Verified Date:
2007-07
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:
DPP
Brief Summary:
A randomized clinical trial was carried out at primary care level in Santiago Chile to investigate a combined treatment for women suffering post-natal depression and preventing the adverse consequences of this illness on infants growth and development
Detailed Description:
Background We compared the effectiveness of a multi-component intervention with usual care to treat postnatal depression among low-income mothers in primary care clinics in Santiago Chile
Methods Randomised controlled trial Two hundred and thirty mothers with major depression attending postnatal clinics were randomly allocated to either a multi-component intervention or usual care The multi-component intervention involved a psychoeducational group treatment adherence support and pharmacotherapy if needed Data were analysed on an intention-to-treat basis The main outcome measure was the Edinburgh Postnatal Depression Scale EPDS at 3 and 6 months after randomisation
Methods Randomised controlled trial Two hundred and thirty mothers with major depression attending postnatal clinics were randomly allocated to either a multi-component intervention or usual care The multi-component intervention involved a psychoeducational group treatment adherence support and pharmacotherapy if needed Data were analysed on an intention-to-treat basis The main outcome measure was the Edinburgh Postnatal Depression Scale EPDS at 3 and 6 months after randomisation
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