- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03565731
Exercise Values of Life and Vitality Everyday (EVOLVE)
A Novel Behavioral Approach for the Adoption and Maintenance of Habitual Physical Activity
The purpose of this study is to develop and test a brief program to help overweight people become more physically active. We plan to design a program that teaches people how to become more active by identifying how fitness enables them to live their lives better.
Participants will be asked to complete questionnaires and wear a device that tracks their exercise for 1 week. If accepted into the study, they will receive a 1 day program designed to help them exercise more. Then they will receive phone calls and emails for support after the program. Finally, participants will come in 3 and 6 months after the program to complete the same questionnaires and wear the exercise tracker again.
The study is primarily interested in increasing exercise levels, and so we hope to see participants exercising more after the program than they were before. We will also ask them questions (via the questionnaires) that tell us the degree to which they are exercising based on their one desires and values, as opposed to doing it because they were told to.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Despite the importance of adoption and maintenance of habitual moderate to vigorous-intensity physical activity (MVPA) for health benefits and long-term weight management, current comprehensive lifestyle interventions place little emphasis on physical activity behavior change strategies and have only modest impact on MVPA. Acceptance and Commitment Therapy (ACT), a well validated, newer generation behavioral approach uses values of clarification and commitment strategies, along with acceptance-based skills training, to effect health behavior change that is consistent with personally identified values. ACT presents a theoretically consistent and potentially powerful intervention framework from which to target values-based autonomous motivation and increase MVPA. The overall aim of this study is to test the feasibility, acceptability, and preliminary efficacy of an ACT-based workshop intervention for increasing bout-related MVPA for overweight and obese, insufficiently active adults using a single-arm design. We will recruit 48 overweight/obese, insufficiently active adults across multiple cohorts and provide them with a 4-hour, ACT-based workshop followed by weekly emails and monthly phone calls for 3 months. The primary goal of the workshop is to use values clarification and acceptance-based skills training to increase values-based autonomous motivation and bout-related MVPA. Participants will self-monitor and report on progress via weekly emails and monthly phone calls. Assessments will be at baseline, 3, and 6 months. The goal of this study is threefold: 1) to determine the feasibility and acceptability of the ACT workshop intervention by assessing the completion of the intervention at all time points and via questionnaires; 2) to show changes in autonomous motivation and values-consistent behavior at the end of the intervention; and 3) to show changes in physical activity, by use of an objectively measured physical activity devices, where participants are engaging in at least 200 minutes of MVPA at 3 and 6-months)
This study will be conducted at the Miriam Hospital Weight Control and Diabetes Research Center by Drs. Jason Lillis and Dale Bond.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Rhode Island
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Providence, Rhode Island, United States, 02903
- The Miriam Hospital Weight Control and Diabetes Research Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Body mass index (BMI) between 25-45 kg/m2
- Report being insufficiently active (i.e., <150 minutes per week of bout related MVPA)
Exclusion Criteria:
- Unable to engage in physical activity safely due to medical status
- Unable to read or understand study materials
- Currently in another physical activity or weight control program
- Currently taking medications that cause dizziness or feeling faint while standing (e.g., some hypertension medications
- Report any condition that would preclude adherence to the intervention protocol (e.g., current or past substance use disorder or psychiatric hospitalization)
- Plans to relocate during the study timeline
- Terminal illness diagnosis
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: ACT-PA Intervention
The primary goal of the intervention is to increase values-based autonomous motivation to increase bout-related MVPA using a single workshop.
Participants will engage in basic and advanced values clarification exercise to help clarify (1) the relative importance of major values domains (e.g.
social, vocational, recreational), and (2) the potential role of PA in empowering functioning in these domains.
Participants will generate their own activity goals and additional values-based goals.
In addition, acceptance strategies will be taught to reduce cognitive and emotional barriers to meeting values-based goals.
Participants will be asked to report progress on goals each week via an automated email survey from a secure project website.
Upon completing the survey, participants will receive standardized responses via email.
Monthly phone calls will be brief, semi-structured, and designed to review key principles and trouble-shoot specific barriers identified by the participant.
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The overall goal of the intervention is to increase bout-related moderate-to-vigorous physical (MVPA) activity to greater than 200 minutes per week.
The basic structure is an initial on-site, group-based intervention workshop, written materials, weekly emails, and monthly phone calls for a total of 3 months.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in bout-related moderate to vigorous physical activity (MVPA)
Time Frame: Change from baseline to 3 and 6 months
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Average daily minutes spent in objectively measured, bout-related MVPA assessed via a multi-sensor activity monitoring device.
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Change from baseline to 3 and 6 months
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Feasibility of the ACT workshop intervention
Time Frame: End of 3-month intervention
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Successful completion of ≥70% of email surveys and intervention phone calls
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End of 3-month intervention
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Acceptability of the ACT workshop intervention
Time Frame: End of 3-month intervention
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An adapted, 15-item version of a previous validated feasibility and acceptability measure for PA interventions with a five-point Likert scale (1 = "don't agree at all" to 5 = "totally agree").
Item examples will include, "I enjoyed participating in the intervention," "I think the intervention strategies were appropriate," and, "I found the lessons to be easy to understand."
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End of 3-month intervention
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Change in autonomous motivation
Time Frame: Change from baseline to 3 and 6 months
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Exercise Self-Regulation Questionnaire.
A 12-item, Likert scaled ("not true at all" to "very true") measure that assesses why a respondent engages in PA by providing several possible reasons that represent varying degrees of autonomous motivation.
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Change from baseline to 3 and 6 months
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Change in values-consistent behavior
Time Frame: Change from baseline to 3 and 6 months
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Comprehensive Assessment of Acceptance and Commitment Therapy Processes Questionnaire.
A 23-item measure with a values subscale that assesses whether individuals are living consistent with their values and what barriers are getting in the way
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Change from baseline to 3 and 6 months
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Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2059-17
- 1R03DK114254 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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