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Community Based Obesity Prevention Among Black Women

Community Based Obesity Prevention Among Black Women

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00938535
Enrollment
194
Registered
2009-07-14
Start date
2009-11-30
Completion date
2014-06-30
Last updated
2014-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Keywords

Obesity, Women's health, Minority health, Obesity prevention

Brief summary

This study will evaluate the efficacy of a behavioral intervention, designed to prevent weight gain among overweight and low obese (25-34.9 kg/m2) Black women (aged 25-44), compared to usual care.

Detailed description

Obesity prevention among Black women is a major public health priority; presently, nearly 54% of the adult Black female population is obese. To date, most intervention attention has been focused on weight reduction among the overweight and obese. However, both conditions are notoriously recalcitrant to treatment, particularly among Blacks. We posit that obesity prevention might represent a particularly effective intervention strategy for overweight Black women. Most studies have shown that Black women have a greater social acceptance of overweight, less body weight dissatisfaction, and higher ideal body weights, compared to Whites. Furthermore, numerous studies have shown that obesity is less lethal and causes fewer co-morbidities among Black vs. White women, suggesting that maintaining overweight may be an appropriate public health goal for Black women. We posit that an intervention approach that emphasizes maintaining overweight, while preventing the transition to obesity will resonate among the target population. Very few obesity prevention RCTs appear in the published literature and, to our knowledge, none have been conducted solely among Black women. We propose to randomize overweight, Black women (n=184) to either usual care (UC) or an obesity prevention (OP) intervention condition. The OP condition is comprised of several intervention components that will be delivered over 12 months; each participant will receive a tailored action plan, tailored print materials, monthly coaching calls, and weekly self-monitoring via an interactive voice response system. Assessments will be taken at baseline, 6, 12, and 18 months post baseline.

Interventions

BEHAVIORALObesity Prevention

This arm includes an action plan, tailored print materials, telephone support calls, interactive self-monitoring, and a 12-month YMCA membership for the participant.

Sponsors

Duke University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 44 Years
Healthy volunteers
No

Inclusion criteria

* African-American * Female * Ages 25-44 * BMI between 25-34.9 kg/m2 * Patients with at least 1 visit in the previous 24 months to a participating Community Health Center

Exclusion criteria

* Not currently pregnant * Not given birth within the past 12 months * No history of myocardial infarction or stroke in last 2 years

Design outcomes

Primary

MeasureTime frame
Change in BMI. We have set a target of BMI maintenance among those randomized to the intervention condition.6, 12 and 18 months post baseline

Secondary

MeasureTime frame
Change in obesity risk behaviors6, 12 and 18 months post baseline
Measures of body composition6, 12 and 18 months post baseline
Psychosocial mediators6, 12 and 18 months post baseline
Obesity related biomarkers6, 12 and 18 months post baseline

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026