- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03465800
Understanding Mechanisms of Exercise Behavior Change
October 18, 2018 updated by: Angela Bryan, University of Colorado, Boulder
This research seeks to examine psychological factors that may impact relationship between incentives and health behavior engagement, specifically physical activity.
Additionally, it will compare the impact of two different incentive schedules on behavior engagement, one providing immediate rewards (i.e.
rewards received on a daily basis) and another providing delayed rewards (i.e.
rewards received at the end of the study period), with an active self-monitoring intervention condition in which no rewards are offered.
Study participants will provide reports of their physical activity each day for three weeks, and in the two incentive conditions, they will receive small monetary rewards for their physical activity.
Following the three week reporting and reward period, participants will complete two additional assessments, measuring psychological constructs and behavior engagement following the cessation of rewards.
The study will also examine how cognitive and anthropomorphic factors may contribute to intervention response and the effects on psychological constructs.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
68
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Colorado
-
Boulder, Colorado, United States, 80309
- University of Colorado Boulder
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Complete less than 150 minutes of moderate-vigorous physical activity weekly
- Daily access to the internet for 3 weeks following baseline research visit
- Have or are willing to create an account on PayPal
- Willing to wear a heart rate monitor watch during physical activity for 3 weeks
- BMI greater than or equal to 25, from self-reported height and weight
Exclusion Criteria:
- Diagnosis of cardiovascular, metabolic, or renal disease
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Self-Monitoring
Participants self-monitor their physical activity
|
self-monitoring of physical activity
|
|
Experimental: Daily Incentives
daily payments for physical activity
|
self-monitoring of physical activity
daily incentive payments for physical activity
|
|
Experimental: Delayed Lump Sum Incentives
lump sum payments for physical activity
|
self-monitoring of physical activity
delayed lump sum payments for physical activity
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Moderate-vigorous physical activity minutes
Time Frame: Week 3
|
summed minutes of weekly moderate intensity physical activity & vigorous intensity physical activity
|
Week 3
|
|
Self-Efficacy for physical activity
Time Frame: Week 3
|
8-item self-report scale measuring self-efficacy (Social Cognitive Theory, Bandura, 1977; also called "perceived behavioral control", Theory of Planned Behavior, Ajzen, 1985); scores are a mean of 8 items, scored 1-7 with higher scores indicative of greater self-efficacy
|
Week 3
|
|
Moderate-vigorous physical activity minutes
Time Frame: Week 5
|
summed minutes of weekly moderate intensity physical activity & vigorous intensity physical activity
|
Week 5
|
|
Self-Efficacy for physical activity
Time Frame: Week 5
|
8-item self-report scale measuring self-efficacy (Social Cognitive Theory, Bandura, 1977; also called "perceived behavioral control", Theory of Planned Behavior, Ajzen, 1985); scores are a mean of 8 items, scored 1-7 with higher scores indicative of greater self-efficacy
|
Week 5
|
|
Attitudes toward physical activity
Time Frame: Week 3
|
12-item self-report scale (Theory of Planned Behavior, Ajzen, 1985); scores are a mean of 12 items scored from -5 to +5, with higher scores indicative of more positive attitudes
|
Week 3
|
|
Attitudes toward physical activity
Time Frame: Week 5
|
12-item self-report scale (Theory of Planned Behavior, Ajzen, 1985); scores are a mean of 12 items scored from -5 to +5, with higher scores indicative of more positive attitudes
|
Week 5
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
February 26, 2018
Primary Completion (Actual)
June 30, 2018
Study Completion (Actual)
July 11, 2018
Study Registration Dates
First Submitted
February 28, 2018
First Submitted That Met QC Criteria
March 13, 2018
First Posted (Actual)
March 14, 2018
Study Record Updates
Last Update Posted (Actual)
October 19, 2018
Last Update Submitted That Met QC Criteria
October 18, 2018
Last Verified
October 1, 2018
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 18-0008
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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