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African American Resilient Caregivers

Not Applicable
Terminated
Conditions
Obesity, Childhood
Interventions
Behavioral: AARC
Registration Number
NCT05711979
Lead Sponsor
Duke University
Brief Summary

The purpose of this pilot study is to test the feasibility of a virtual intervention to prevent child obesity and cardiovascular disease in African American families.

Detailed Description

African American children experience a high prevalence of child obesity, increasing their subsequent risk of cardiovascular disease and diabetes. There is a lack of effective obesity prevention interventions for this population. Investigators also know that African American parents and caregivers experience high levels of stress and the manifestations of stress for African American women in particular may be unique and specific. Parent stress can lead to unhealthy family behaviors including less physical activity and a less healthy diet for parents and children. Given this background the investigators are creating a new intervention that combines an adapted evidence-based obesity prevention program (Competency Based Approach to Community Health - COACH) with mindfulness-based stress reduction tailored to African American women. As an initial step the investigators will pilot the intervention in a small number of African American women to determine whether the program is feasible.

Recruitment & Eligibility

Status
TERMINATED
Sex
Female
Target Recruitment
4
Inclusion Criteria
  • Identify as African American and female
  • Have a child between the ages of 2-5 who lives with them at least 4 days per week that they care for as a parent or guardian.
  • Feel comfortable discussing personal experiences and goals related to diet, PA, stress, parenting, etc. in front of a group of peers
  • Access to zoom, preferably with video
Exclusion Criteria

• Non English Speaking

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
AARC InterventionAARCParticipants in the AARC Intervention Arm will receive a 10 week intervention.
Primary Outcome Measures
NameTimeMethod
Acceptability as assessed by semi-structured interviews10 weeks (post intervention)

In this pilot study, acceptability of the intervention to the study population will be assessed by semi-structured interviews. Interview questions will identify features of the intervention which were beneficial to participants as well as barriers to participation.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Duke University Health System

🇺🇸

Durham, North Carolina, United States

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