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N/A N=128 Randomized Single-blind Health Services Research

Care After Pregnancy Study (CAPS): Engaging Women in Postpartum Care

Postpartum Care

Enrolled (actual)
128
Serious AEs
0.0%
Results posted
Oct 2022
Primary outcome: Primary: Number of Participants Using a Non-barrier Method of Contraception — 24; 29; 22 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Healthy Beyond Pregnancy (Behavioral); Pre-Scheduled Postpartum Visit (Behavioral); Attention Control (Other)
Age
Pediatric, Adult · 12+ yrs
Sex
Female
Sponsor
University of Pittsburgh
Primary completion
Jun 2021

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants Using a Non-barrier Method of Contraception
19; 26; 22
PRIMARY
Number of Participants Using a Non-barrier Method of Contraception
19; 26; 22
PRIMARY
Adherence of Postpartum Visit
25; 25; 23
SECONDARY
The Number of Participants Who Given Their Infant Breast Milk
5; 3; 3; 18; 16; 13
SECONDARY
The Number of Participants Who Given Their Infant Breast Milk
5; 3; 3; 18; 16; 13
SECONDARY
The Number of Participants Who Given Their Infant Breast Milk
5; 3; 3; 18; 16; 13
SECONDARY
The Number of Participants Who Given Their Infant Breast Milk
5; 3; 3; 18; 16; 13

Summary

The overarching hypothesis of our research agenda is that an intervention that engages economically disadvantaged women in personalized postpartum care will promote equality in maternal child health. As a first step to test our hypothesis the investigators propose the following aims: Specific Aim 1: Measure the impact of Healthy Beyond Pregnancy on key components of postpartum care, including use of effective contraception at three and six months postpartum and breastfeeding duration at three and six months. Specific Aim 2: Determine if Healthy Beyond Pregnancy improves adherence to health screening and linkage to follow-up care for women with cardio-metabolic complications of pregnancy.

Eligibility Criteria

Inclusion Criteria

  • Insured by a PA Medicaid insurance
  • Pregnancy care in the Magee Womens Hospital Outpatient Clinic

Exclusion Criteria

  • Delivery less than 24 weeks
  • Fetal or neonatal demise
  • Women who had a postpartum tubal ligation
  • Women less than 18 year of age
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04257552). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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