Postpartum Depression Prevention Trial

NACompletedINTERVENTIONAL
Enrollment

702

Participants

Timeline

Start Date

August 31, 2004

Primary Completion Date

April 30, 2007

Study Completion Date

April 30, 2007

Conditions
Postpartum Depression
Interventions
BEHAVIORAL

Peer support

Mothers allocated to the peer support group had access to all of the standard community postpartum services in addition to having received telephone-based support from a peer volunteer (a mother who has previously experienced, and recovered from, postpartum depression and has participated in a 4-hour training session). Telephone contact with a new mother was initiated within 48 to 72 hours of trial enrolment and then as frequently as the dyad deemed necessary; a minimum of four contacts were required.

Trial Locations (7)

P3E 3A3

Sudbury & District Health Unit, Greater Sudbury

L5R 4B2

Peel Health Department, Mississauga

L6M 3L1

Halton Region Health Department, Oakville

K2G 6J8

Ottawa Public Health, Ottawa

L4B 4N7

York Region Health Services, Richmond Hill

M2N 5V7

Toronto Public Health, Toronto

N9J 4J8

Windsor Essex County Health Unit, Windsor

All Listed Sponsors
collaborator

Canadian Institutes of Health Research (CIHR)

OTHER_GOV

lead

University of Toronto

OTHER

NCT00604604 - Postpartum Depression Prevention Trial | Biotech Hunter | Biotech Hunter