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Clinical Trials/NCT04937205
NCT04937205
Completed
Not Applicable

Understanding Motivation for Exercise to Enhance Physical Activity Adherence in Adults With Obesity

University of Colorado, Denver1 site in 1 country39 target enrollmentStarted: February 13, 2019Last updated:
ConditionsObesity

Overview

Phase
Not Applicable
Status
Completed
Enrollment
39
Locations
1
Primary Endpoint
Acceptability

Overview

Brief Summary

The limited success of our current approaches to increase adoption and maintenance of physical activity in adults with overweight and obesity is a substantial barrier to effectively address the current obesity epidemic. This mentored F32 application addresses the significant public health issue of obesity and associated risk of major chronic diseases by using mixed methods research to optimize an innovative, theoretically based physical activity intervention designed to enhance motivation for exercise in adults with overweight and obesity.

Detailed Description

Physical activity (PA) is one of the best predictors of sustained weight loss and current guidelines recommend high levels of PA to prevent weight regain after weight loss. However, long-term adherence to PA is generally poor when adults with overweight/obesity are provided an exercise prescription consistent with current guidelines. Thus, it is essential to evaluate novel strategies to enhance adoption and maintenance of PA in adults with overweight/obesity. The overall goal of this mentored F32 application is to use mixed methods research to optimize an innovative, theoretically based PA intervention designed to enhance motivation for exercise in adults with overweight/obesity. Specifically, the objectives of this proposal are to evaluate and optimize a theory-based PA intervention (called MOVE) designed to enhance motivation for exercise as a sub-study of an ongoing weight loss "parent" trial (COMIRB, Protocol #17-0369). In Aim 1, adults from an ongoing behavioral weight loss trial (R01DK111622) will receive the MOVE intervention and participate in focus groups to explore how participants experience MOVE. In Aim 2, we will use a mixed methods convergent design to integrate quantitative results from a secondary data analysis and qualitative results (Aim 1) to optimize MOVE in preparation for a full evaluation of MOVE in a future randomized controlled study.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 60 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • A current study participant randomized to the parent trial in cohorts 2-4 for COMIRB, Protocol #17-0369
  • Completed at least 2 of 3 MOVE program components (attended ≥80% of either group-based class and/or attended the one-on-one support session).

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Acceptability

Time Frame: weeks 21-30

During a 90-minute semi-structured focus group, participants were asked about their satisfaction with major aspects of the MOVE physical activity support program including: 1) MOVE content and 2) delivery of MOVE content including meeting frequency and structure for both group-based and 1:1 meetings. Participants were also asked about their overall experience with the MOVE program, things that worked well, things that did not work well, and about the most important things they learned from the MOVE program.

Secondary Outcomes

  • Motivation for Physical Activity(weeks 21-30)
  • Motivation for Sedentary Behavior(weeks 21-30)
  • Barriers to Physical Activity(weeks 21-30)
  • Perceptions of Physical Activity Messages(weeks 21-30)
  • Influence of Diet on Physical Activity Adherence(weeks 21-30)
  • Facilitators to Physical Activity(weeks 21-30)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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