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

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.

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

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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