MedPath

Weight Management in Mothers and Adult Daughters

Not Applicable
Completed
Conditions
Overweight or Obese
Interventions
Behavioral: Communication
Behavioral: Standard
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
Arm && Interventions
GroupInterventionDescription
CommunicationCommunicationBehavioral weight loss program with communication skills training
StandardStandardStandard behavioral weight loss program
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

© Copyright 2025. All Rights Reserved by MedPath