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Translating Research Into Practice for Postpartum Depression

Practice Based Clinical Trial of Screening, Diagnosis and Follow up Management for Postpartum Depression in Family Medicine Practices.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00548743
Acronym
TRIPPD
Enrollment
3000
Registered
2007-10-24
Start date
2005-09-30
Completion date
2010-08-31
Last updated
2007-12-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum Depression

Keywords

Depression, Postpartum, Dyad satisfaction, Parenting comfort, Screening, Management, Follow up, Primary care, Practice based research

Brief summary

This is a study to assess the impact of introducing screening and planned follow up for postpartum depression. All women ages 18 to 45 who speak English or Spanish who come to the enrolled community family medicine offices will either be given usual care or screened using the Edinburgh Postnatal Depression Screening tool. If the EDPS score is high the women will be given the PHQ-9 to more clearly identify the specific likelihood of being depressed. Women who are determined to be depressed will be treated with medication or counseling based on the preference of the women and their physicians. Women will be followed through nurse initiated phone calls and visits to the physicians office. Outcomes include the level of depression symptoms, measure of comfort with parenting, and satisfaction with partner relationships comparing baseline levels with those at 6 and 12 months from the usual care and intervention sites. These data will be collected by questionnaire. In addition, with the women's permission, medical records will be reviewed.

Detailed description

A randomized controlled trial of screening and management of postpartum depression that includes a second phase assessing the maintenance of the intervention in the original intervention sites and a switch from usual care to intervention in the control sites. Planned enrollment includes 29 family medicine practices and 3000 women over a period of four years. All follow up and management is initiated within the family medicine practices to improve generalizability and likelihood for dissemination. In addition to the patient centered outcomes, exploratory analyses will look at the uptake and degree of implementation and maintenance of the intervention based on characteristics of the practice including size, location, affiliation with larger group, type of practice and whether or not the practice is a community health center or residency practice.

Interventions

BEHAVIORALScreening and follow up

Two stage screening with EPDS and PHQ-9, treatment for depression at physician's discretion and follow up phone calls and visits

BEHAVIORALUsual care

usual care for identification and management of postpartum depression

Sponsors

Olmsted Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SCREENING
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* 5 to 12 weeks postpartum * Able to speak and read English or Spanish * 18 to 45 years of age

Exclusion criteria

* Significant cognitive impairment and unable to answer screening questions

Design outcomes

Primary

MeasureTime frame
Level of depressive symptoms and level of parenting comfort12 months postpartum

Secondary

MeasureTime frame
Percent eligible women screened and of those screen positive, percent treated and followed according to protocol12 months for each women

Countries

United States

Contacts

Primary ContactBarbara P Yawn, MD MSc
byawn@olmmed.org507 287 2758
Backup ContactSusan M Bertram, RN MSN
sbertram@olmmed.org888 292 7164

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026