MedPath

Weight Management in Mothers and Adult Daughters

Not Applicable
Completed
Conditions
Overweight or Obese
Registration Number
NCT02787902
Lead Sponsor
University of California, San Diego
Brief Summary

The purpose of this study is to develop, implement, and evaluate a behavioral weight management intervention with a communication training component for Mexican-American women. The study has three specific aims.

Aim 1: Develop a behavioral weight loss intervention that modifies evidence-based behavioral weight loss treatment using results from formative data collected from Mexican-American mother-daughter dyads. The adapted intervention will focus on improving dyadic communication and collaboration for providing reciprocal support for healthy eating and physical activity behaviors.

Aim 2: Implement and evaluate a pilot weight management program adapted for mother-daughter dyads. Dyads will be randomly assigned to partner-based treatment with or without communication skills training.

Aim 3: Evaluate associations between changes in weight, weight-related behaviors, and psychosocial variables with changes in measures assessing interpersonal communication.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
54
Inclusion Criteria
  • Female
  • Body mass index of 25-50 kg/m2
  • Mexican or Mexican-American
Exclusion Criteria
  • Pregnancy or plans to become pregnant in the next year
  • 5% weight loss in the last 3 months
  • History of bariatric surgery
  • Serious medical condition or psychological disorder

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Weight change16 weeks

Change in weight from baseline to post-intervention (16 weeks).

Secondary Outcome Measures
NameTimeMethod
Blood pressurebaseline and post-intervention (16 weeks)
Communicationbaseline and post-intervention (16 weeks)
Weight control behaviorbaseline and post-intervention (16 weeks)
Anthropometricsbaseline and post-intervention (16 weeks)
Psychosocial factorsbaseline and post-intervention (16 weeks)
Eating behaviorbaseline and post-intervention (16 weeks)
Physical activitybaseline and post-intervention (16 weeks)
Treatment attendance and adherencebetween baseline and post-intervention (16 weeks)
Relationship factors (dyad, family, social networks)baseline and post-intervention (16 weeks)

Trial Locations

Locations (1)

University of California San Diego

🇺🇸

La Jolla, California, United States

University of California San Diego
🇺🇸La Jolla, California, United States

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