- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04618757
Trial Evaluating Hedonic vs Cash Incentives (TEH-C)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The evidence is overwhelming that sustained physical activity reduces risks for non-communicable diseases, increases longevity, and reduces medical costs. Yet, the rates of physical activity have been steadily decreasing such that physical inactivity is now the fourth leading cause of death worldwide. In Singapore, 33% of adults are insufficiently active despite Singapore being a highly walkable city with numerous subsidized community-based physical activity programs. A review of the literature shows that, to date, no study has directly compared cash versus hedonic rewards for health behavior change despite theory suggesting hedonic rewards may work better. Furthermore, hedonic rewards can often be purchased at lower cost than their cash equivalent. This makes hedonic rewards potentially more cost-effective if they are proven to be at least as effective at increasing positive behavior change compared to giving the same value in cash.
Thus, we aim to determine, using a randomized trial with two parallel arms, whether hedonic rewards (Arm 1) can be more effective than their cash equivalent (Arm 2) in promoting increases in physical activity, assessed via step counts measured by a Fitbit physical activity tracker, during a 4-calendar month intervention. We hypothesize that the average proportion of months meeting the incentivized step target across participants will be greater for those in the hedonic incentive arm as compared to those in the cash incentive arm (primary outcome).
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Singapore, Singapore, 169857
- Duke-NUS Medical School
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Aged between 21 to 70 years inclusive.
- Singapore resident (residing in Singapore during the study period [up to 5 months])
- English-speaking and English literate
- Smartphone-literate
Exclusion Criteria:
- Pregnant or lactating
- Unable to walk up 10 steps (individual steps, not floors) without stopping
- Currently on doctor's advice against engaging in moderate-to-vigorous physical activity (i.e., brisk walking or more intense).
- Currently have a condition(s) that restricts engaging in moderate-to-vigorous physical activity (i.e., brisk walking or more intense).
- Unwilling to be randomized into study arms
- Unwilling to use a Fitbit for the study period (up to 5 calendar months)
- Unwilling to pay the $20 enrolment fee
- Does not complete the Consent Form
- Refuses to give consent to participate in the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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Experimental: Hedonic Reward
Participants' reward for meeting monthly step targets is in the form of reimbursements of up to $50 for expenses on hedonic activities of their choice
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Fitbit devices are wireless pedometers that track the steps of participants, and will be offered in conjunction with a tailored website with customized information for participants.
Other Names:
A reimbursement credit for hedonic expenses worth up to $50 will be awarded to each participant if they log at least 10,000 daily steps on at least 25 days during the first 28 days of each calendar month on Fitbit activity trackers provided by the study.
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Experimental: Cash Reward
Participants' reward for meeting monthly step targets is in the form of $50 cash disbursements
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Fitbit devices are wireless pedometers that track the steps of participants, and will be offered in conjunction with a tailored website with customized information for participants.
Other Names:
A reimbursement credit for $50 in cash will be awarded to each participant if they log at least 10,000 daily steps on at least 25 days during the first 28 days of each calendar month on Fitbit activity trackers provided by the study.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Proportion of months in meeting the step target
Time Frame: Months 1-4
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The mean proportion of months meeting the incentivized targets (i.e. at least 10,000 daily steps on at least 25 days during the first 28 days of each calendar month via step counts measured by Fitbit, during a 4 calendar month intervention) across participants.
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Months 1-4
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Difference in mean daily steps between the 2 intervention arms
Time Frame: Months 1-4
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Difference in mean daily steps between intervention arms for the first 28 days of each of 4 intervention months, controlling for baseline daily values.
These will be measured via step counts measured by Fitbit.
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Months 1-4
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Difference in median daily steps between the 2 intervention arms
Time Frame: Months 1-4
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Difference in median daily steps between intervention arms for the first 28 days of each of 4 intervention months, controlling for baseline daily values.
These will be measured via step counts measured by Fitbit.
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Months 1-4
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Difference in mean Fitbit fairly and very active minutes between the 2 intervention arms
Time Frame: Months 1-4
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Difference in mean Fitbit fairly and very active minutes between intervention arms for the first 28 days of each of 4 intervention months, controlling for baseline daily values.
The Fitbit fairly and active minutes count towards Fitbit "active minutes", which are determined by Fitbit's proprietary algorithms and are defined as sustained activity of ≥10-minute bouts.
These will be measured via step counts measured by Fitbit.
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Months 1-4
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Difference in median Fitbit fairly and very active minutes between the 2 intervention arms
Time Frame: Months 1-4
|
Difference in median Fitbit fairly and very active minutes between intervention arms for the first 28 days of each of 4 intervention months, controlling for baseline daily values.
The Fitbit fairly and active minutes count towards Fitbit "active minutes", which are determined by Fitbit's proprietary algorithms and are defined as sustained activity of ≥10-minute bouts.
These will be measured via step counts measured by Fitbit
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Months 1-4
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Eric A Finkelstein, Ph.D, M.H.A, Duke-NUS Graduate Medical School
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
- NIHA-2018-002 (Study 1)
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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