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Clinical Trials/NCT05796141
NCT05796141
Recruiting
N/A

Optimizing a Couples-Based mHealth Intervention for Weight Management

University of Connecticut1 site in 1 country736 target enrollmentMarch 13, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Overweight and Obesity
Sponsor
University of Connecticut
Enrollment
736
Locations
1
Primary Endpoint
Body Weight (kg)
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The goal of this project is to investigate how to enhance the effects of an online-only (mHealth) couples weight loss program. This study will use an innovative methodological framework, the Multiphase Optimization Strategy (MOST), to test four different strategies for weight loss and partner support in addition to a core intervention (i.e., dyadic action planning, joint feedback on goal progress, autonomy support training, and home environment modifications).

Registry
clinicaltrials.gov
Start Date
March 13, 2024
End Date
November 2026
Last Updated
last year
Study Type
Interventional
Study Design
Factorial
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Amy Gorin

Vice Provost for Health Sciences and Interdisciplinary Initiatives

University of Connecticut

Eligibility Criteria

Inclusion Criteria

  • Married/cohabitating couple - both partners must be eligible
  • BMI between 25-55kg/m2
  • English speaking/reading
  • Have a smartphone and reliable internet access
  • Have active email address
  • Willing to videoconference

Exclusion Criteria

  • Report being unable to walk 2 blocks without stopping
  • Are currently participating in weight loss treatment, have a history of bariatric surgery, or lost ≥5% in the past 6-months
  • Are pregnant or plan to become pregnant during the study period
  • Report chest pain or loss of consciousness on the Physical Activity Readiness Questionnaire
  • Report a medical condition that could jeopardize their safety in a weight control program with diet and exercise guidelines
  • Report conditions that, in the judgment of the PI, would render them unlikely to follow the protocol (e.g. dementia)

Outcomes

Primary Outcomes

Body Weight (kg)

Time Frame: Baseline to 6 months

Weight change from baseline to 6 months. Weight will be objectively measured on a digital scale in the participant's home and weight change will be calculated.

Secondary Outcomes

  • Transactive Density(Baseline, 3 months, 6 months)
  • Physical Activity (Paffenbarger Physical Activity Questionnaire)(Baseline, 3 months, 6 months)
  • Home Food Environment (Household Food Inventory)(Baseline, 3 months, 6 months)
  • Dietary Intake(Baseline, 3 months, 6 months)
  • Goal Coordination (Wingrove Goal Coordination Scale)(Baseline, 3 months, 6 months)
  • Shared Goal Representation(Baseline, 3 months, 6 months)
  • Home Exercise Environment (Exercise Environment Questionnaire)(Baseline, 3 months, 6 months)

Study Sites (1)

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