Expired Study
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Rochester, Minnesota 55904


Purpose:

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.


Study summary:

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.


Criteria:

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


NCT ID:

NCT00548743


Primary Contact:

Principal Investigator
Barbara P Yawn, MD MSc
Olmsted Medical Center

Barbara P Yawn, MD MSc
Phone: 507 287 2758
Email: byawn@olmmed.org


Backup Contact:

Email: sbertram@olmmed.org
Susan M Bertram, RN MSN
Phone: 888 292 7164


Location Contact:

Rochester, Minnesota 55904
United States



There is no listed contact information for this specific location.

Site Status: Recruiting


Data Source: ClinicalTrials.gov

Date Processed: November 21, 2017

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