ClinicalTrials.Veeva

Menu

African American Resilient Caregivers (AARC)

Duke University logo

Duke University

Status

Terminated

Conditions

Obesity, Childhood

Treatments

Behavioral: AARC

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT05711979
Pro00111805

Details and patient eligibility

About

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.

Full 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.

Enrollment

4 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Prevention

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

4 participants in 1 patient group

AARC Intervention
Experimental group
Description:
Participants in the AARC Intervention Arm will receive a 10 week intervention.
Treatment:
Behavioral: AARC

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems