Overweight or Obese Clinical Trial
Official title:
Improving Communication and Collaboration for Weight Management in Mother-daughter
NCT number | NCT02787902 |
Other study ID # | 151345 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | August 1, 2018 |
Est. completion date | December 31, 2020 |
Verified date | October 2021 |
Source | University of California, San Diego |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 54 |
Est. completion date | December 31, 2020 |
Est. primary completion date | December 31, 2020 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 18 Years to 65 Years |
Eligibility | 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 |
Country | Name | City | State |
---|---|---|---|
United States | University of California San Diego | La Jolla | California |
Lead Sponsor | Collaborator |
---|---|
University of California, San Diego |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Weight change | Change in weight from baseline to post-intervention (16 weeks). | 16 weeks | |
Secondary | Anthropometrics | baseline and post-intervention (16 weeks) | ||
Secondary | Blood pressure | baseline and post-intervention (16 weeks) | ||
Secondary | Communication | baseline and post-intervention (16 weeks) | ||
Secondary | Relationship factors (dyad, family, social networks) | baseline and post-intervention (16 weeks) | ||
Secondary | Psychosocial factors | baseline and post-intervention (16 weeks) | ||
Secondary | Eating behavior | baseline and post-intervention (16 weeks) | ||
Secondary | Physical activity | baseline and post-intervention (16 weeks) | ||
Secondary | Weight control behavior | baseline and post-intervention (16 weeks) | ||
Secondary | Treatment attendance and adherence | between baseline and post-intervention (16 weeks) |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT00011193 -
Dose-Response to Exercise in Women Aged 45-75 Years (DREW)
|
||
Recruiting |
NCT05583578 -
HOMEStudy: Development of a Home-based Self-delivered Prehabilitation Intervention to Proactively Reduce Fall Risk in Older Adults
|
N/A |