Understanding Mechanisms of Health Behavior Change

July 27, 2023 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 fruit and vegetable consumption. 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 a control condition in which no rewards are offered. Study participants will provide reports of their fruit and vegetable consumption each day for three weeks, and in the two incentive conditions, they will receive small monetary rewards for their fruit and vegetable consumption. 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

Description

Inclusion Criteria:

  • Consume fewer than 3 servings/day of fruits and vegetables
  • Daily access to internet for 3 weeks following baseline session
  • Have or are willing to create an account on PayPal
  • BMI greater than or equal to 25, from self-reported height and weight

Exclusion Criteria:

-

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 Control
Daily tracking of fruit and vegetable consumption
recording fruit and vegetable consumption
Experimental: Daily Incentives
Incentives for fruit and vegetable consumption delivered daily
recording fruit and vegetable consumption
daily payments for consuming fruits and vegetables
Experimental: Delayed Lump Sum Incentives
Incentives for fruit and vegetable consumption delivered in a lump sum at the end of the intervention
recording fruit and vegetable consumption
lump sum payments for consuming fruits and vegetables

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Fruit and vegetable consumption, servings per week
Time Frame: 3 Weeks
3 Weeks
Fruit and vegetable consumption, servings per week
Time Frame: 5 Weeks
5 Weeks
Perceived behavioral control scale score
Time Frame: 3 Weeks
3 Weeks
Perceived behavioral control scale score
Time Frame: 5 Weeks
5 Weeks
Attitude scale score
Time Frame: 3 Weeks
3 Weeks
Attitude scale score
Time Frame: 5 Weeks
5 Weeks

Secondary Outcome Measures

Outcome Measure
Time Frame
Intrinsic motivation scale score
Time Frame: 3 Weeks
3 Weeks
Intrinsic motivation scale score
Time Frame: 5 Weeks
5 Weeks

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)

July 13, 2017

Primary Completion (Actual)

February 21, 2018

Study Completion (Actual)

March 30, 2018

Study Registration Dates

First Submitted

June 16, 2017

First Submitted That Met QC Criteria

June 16, 2017

First Posted (Actual)

June 20, 2017

Study Record Updates

Last Update Posted (Actual)

August 1, 2023

Last Update Submitted That Met QC Criteria

July 27, 2023

Last Verified

July 1, 2023

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 16-0700

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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