- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01282944
Encouraging Walking in Older Adults
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This pilot study is a randomized controlled trial of incentive schemes delivered through a novel internet-based platform to promote walking in older adults. The four arms consist of the following: financial incentives, peer network, combined arm (financial incentive & peer network), and control.
Participation in the study will last approximately 26 weeks, including the 2-week run-in period, 4-month intervention period, and 2-month follow-up period.
The primary goals of the study are:
To test the effects of financial incentives on older adults uptake and retention of increased levels of walking.
Hypothesis1a: Participants receiving financial incentives will increase their number of steps per day more than participants not receiving financial incentives.
To test the effects of connection to a new peer network on older adults uptake and retention of increased levels of walking.
Hypothesis 2a: Participants connected to a new peer network of other participants will increase their number of steps per day more than participants not connected to a new network.
Hypothesis 2b: Participants connected to a new peer network of other participants will retain increases in their number of steps per day more than participants not connected to a new network.
To test the combined effects of financial incentives and peer networks on older adults' uptake and retention of increased levels of walking.
Hypothesis 3a: Participants who receive financial incentives and are connected to a peer network will increase their number of steps per day more than participants who are only connected to a peer network.
Hypothesis 3b: Participants who receive financial incentives and are connected to a peer network will more effectively maintain increases in number of steps per day as compared with participants who only receive financial incentives.
- To develop internet, text and email messaging, and pedometer-internet interface technologies to build peer networks and provide regular feedback to subjects.
Hypothesis 4: The study platform will provide an effective mechanism for subject recruitment, data collection, communication and regular feedback.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Pennsylvania
-
Philadelphia, Pennsylvania, United States, 19104
- University of Pennsylvania
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Adult 65 years of age or older
- Communicates primarily in English
- Personal computer with high-speed internet connection and functional Universal Serial Bus (USB) port
- Able to walk 1/4 mile (i.e., 2 to 3 blocks) without stopping
- Currently engaging in less than 150 minutes moderate intensity exercise & less than 75 minutes vigorous intensity exercise each week
- No pedometer use in last 30 days
- Planning to stay in area for study duration
Exclusion Criteria:
- Myocardial infarction, stroke, transient ischemic attack, major cardiovascular surgery, deep venous thrombosis, or pulmonary embolus in the last 6 months
- New York Heart Association Class III or IV heart failure; severe aortic stenosis; history of cardiac arrest, use of cardiac defibrillator; or severe angina
- Hip fracture, total hip replacement, total knee replacement or spinal surgery in the last 6 months
- Uncontrolled hypertension
- Lung disease requiring supplemental oxygen
- Diabetes mellitus requiring insulin therapy
- Severe osteoarthritis or rheumatoid arthritis
- End stage renal disease requiring hemodialysis
- Movement disorder (e.g., Parkinson's disease)
- Dementia (e.g., Alzheimers Disease, Lewy-Body Dementia, Multi-Infarct Dementia, Picks Disease, Binswangers Disease, Frontotemporal Dementias, Parkinsons Disease Dementia, Huntingtons Disease, Dementia in HIV/AIDS, Wernicke-Korsakoff syndrome, Creutzfeldt-Jakob disease)
- Major psychiatric disorder (e.g., schizophrenia or bipolar disorder)
- Current consumption of ≥ 14 alcoholic drinks per week
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Combined Financial Incentive & Peer Network Arm
Daily use of pedometer for 6 months. Walking goal set based on level of walking during 2 week run-in period. Subjects connected with 4 other participants in the same study arm to form a peer network of 5 individuals. Each peer network participant given access to a secure online message board that will allow the 5 participants in each peer network to communicate online. Participants also receive weekly feedback regarding which participants in the peer group achieved their walking goals during the previous week. Each week, if pedometer is used and walking goal is met for 5 out of 7 days, participant will be entered in lottery with an approximate 3 in 10 chance of winning $50 and an approximate 3 in 100 chance of winning $200. Financial incentive and peer network terminated after 4 months. Daily use of pedometer continues for an additional 2 months. |
Lottery with an approximate 3 in 10 odds of earning $50 and an approximate 3 in 100 odds of earning $200.
Subjects will be connected with 4 other participants in the same study arm to form a peer network of 5 individuals.
|
|
No Intervention: Active Control
Daily use of pedometer for 6 months. Walking goal set based on level of walking during 2 week run-in period. Weekly feedback provided on meeting walking goal - defined as achieving goal number of steps for 5 of 7 days per week. Subjects in the Control Group will only receive pedometers and weekly feedback on their performance through the same mechanisms and with the same frequency as participants in the other three study arms. There will be no financial incentives or peer networks in this group. |
|
|
Experimental: Financial Incentive Arm
Daily use of pedometer for 6 months.
Walking goal set based on level of walking during 2 week run-in period.
Weekly feedback provided on meeting walking goal - defined as achieving goal number of steps for 5 of 7 days per week.
Each week, if pedometer is used and walking goal is met for 5 out of 7 days, participant will be entered in lottery with an approximate 3 in 10 chance of winning $50 and an approximate 3 in 100 chance of winning $200.
Financial incentive is terminated after 4 months.
Daily use of pedometer continues for an additional 2 months.
|
Lottery with an approximate 3 in 10 odds of earning $50 and an approximate 3 in 100 odds of earning $200.
|
|
Experimental: Peer Network Arm
Daily use of pedometer for 6 months. Walking goal set based on level of walking during 2 week run-in period. Weekly feedback provided on meeting walking goal - defined as achieving goal number of steps for 5 of 7 days per week. Subjects will be connected with 4 other participants in the same study arm to form a peer network of 5 individuals. Each peer network participant will be given access to a secure online message board that will allow the 5 participants in each peer network to communicate online. All participants in a peer network will receive a list of ways in which his or her new network could support each individual's walking goals. Participants will also receive weekly feedback regarding which participants in the peer group were successful in achieving their walking goals during the previous week. Peer network is terminated after 4 months. Daily use of pedometer continues for an additional 2 months. |
Subjects will be connected with 4 other participants in the same study arm to form a peer network of 5 individuals.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
mean proportion of days that step per day goals were attained
Time Frame: 16 weeks
|
16 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
mean number of steps per day
Time Frame: 16 weeks
|
16 weeks
|
|
mean proportion of days that step per day goals were attained during follow-up
Time Frame: 8 weeks
|
8 weeks
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Jason Karlawish, MD, University of Pennsylvania
- Study Director: Jeffrey T Kullgren, MD, MPH, kullgren@mail.med.edu
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 812090
- RC2AG036592 (U.S. NIH Grant/Contract)
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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