Community-based Implementation of Adapted STAC
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Wisconsin, Madison
About this trial
This study is being done to adapt the Staying Healthy After Childbirth (STAC) intervention for implementation among Black Women and Birthing Persons (WBP).
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Belong to the STAC-CAB or Lived Experience Group
Aged 18 or older
Staff of CBO participating in PDSA cycle
Aged 18 years or older
Disqualifiers
Persistent second or third trimester bleeding at time of enrollment
Premature rupture of membranes in the current pregnancy at time of enrollment
Known unrepaired maternal congenital heart disease requiring surgical correction
Maternal heart failure
Trial design
Design model
Single group
Treatments tested in this trial
PDSA Cycles
Other interventionConduct PDSA cycles and follow-up interviews and surveys for patients (3-5 per cycle, 10 total) and CBO staff (no less than 2)
Treatment groups
46 Participants
are divided into 3 treatment groupsGroup A: STAC-CAB MembersNo intervention 0 interventions
Group B: Lived Experience Group MembersNo intervention 0 interventions
Group C: PDSA Cycle Participants and CBO StaffExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Qualitative Summary of Barriers to Implementation of A-STAC
Barriers to implementation of A-STAC in CBOs will be investigated via qualitative analysis of interviews and focus groups with STAC-CAB members. All feedback regarding barriers will be coded for themes summarized by participant count.
Time frame
up to 4 weeks2
Qualitative Summary of Facilitators to Implementation of A-STAC
Facilitators to implementation of A-STAC in CBOs will be investigated via qualitative analysis of interviews and focus groups with STAC-CAB members. All feedback regarding facilitators will be coded for themes summarized by participant count.
Time frame
up to 4 weeks3
Qualitative Summary of Adaptations to STAC
Adaptations to STAC will be analyzed from patient participant interviews and CBO staff participants post-PDSA cycles. Interviews will be coded for themes summarized by count.
Time frame
up to 8 weeks4
The Acceptability of Intervention Measure (AIM)
The Acceptability of Intervention Measure (AIM) measures intervention acceptability with 4 items ranked on a 5-point Likert-type scale from 1 = Completely Disagree to 5 = Completely Agree. Higher scores indicate higher acceptability.
Time frame
up to 8 weeksSponsors and contacts
Click on the lead sponsor to view all of their trials.
University of Wisconsin, Madison
Lead sponsor
Centers for Disease Control and Prevention
Collaborator
Source ClinicalTrials.gov