Testing Feasibility of Care Coordination and Motivational Interviewing for Women With a Recent Preterm Birth

Part of paid clinical trials in Philadelphia, Pennsylvania.

Sponsor
Children's Hospital of Philadelphia
Study ID
NCT05120843
Status
Terminated

Conditions

  • Contraceptive Usage
  • Depression
  • Health Care Utilization
  • Preterm Birth
  • Tobacco Use
  • Weight, Birth

Eligibility Criteria

Sex
FEMALE
Age
14 Years - 45 Years
Healthy Volunteers
Accepted

Interventions

  • Care coordination and motivational interviewing — BEHAVIORAL
    Interventionist will engage participants in care planning, health education, health care navigation, screening for unmet health needs or social needs, and motivational interviewing. The final intervention is expected to be six months in duration. However during this single-arm open testing phase, some participants may receive only key components of the intervention in order to assess feasibility, reach, adoption, and fidelity of those components.

Study Details

This study continues an adaptation of care coordination to address the needs of women after preterm birth. This is a small single arm open trial designed to test intervention implementation and refine the intervention before ongoing feasibility testing.

Key Dates

Start date
Feb 3, 2022
Status verified
Jan 2026
Primary completion
Sep 23, 2023
Completion
Sep 23, 2023

Study Design

Enrollment
13 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION

Arms

  • Other: Intervention Arm
    This intervention will combine care coordination and motivational interviewing strategies.

Primary Outcome Measure

Screening Rate (Feasibility) [ Time Frame: Screening phase (Up to 1 week prior to enrollment) ]

Locations (1)

FacilityCityStateZIPSite coordinators
Hospital of the University of PennsylvaniaPhiladelphiaPennsylvania19104-

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