Peripheral Artery Disease Clinical Trial
Official title:
The Effect of opt-in Versus Opt-out Framing on Clinical Trial Enrollment Among Patients With Peripheral Artery Disease
Verified date | June 2024 |
Source | University of Pennsylvania |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
It is uncertain whether opt-out framing will increase participation in a clinical trial intended to promote physical activity in patients with peripheral artery disease (PAD). This study will test whether opt-in or opt-out framing of study participation upon initial contact affects the proportion of patients who ultimately enroll in the study and the demographic characteristics of enrolled patients.
Status | Active, not recruiting |
Enrollment | 1200 |
Est. completion date | July 1, 2024 |
Est. primary completion date | July 25, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - At least 18 years of age - Have been seen in the University of Pennsylvania Health System - Have an ICD-10 code consistent with peripheral artery disease (I70.2x, I70.3x-I70.7x, I73.9) or peripheral artery disease on their problem list - Have an email address on file with the University of Pennsylvania Health System Exclusion Criteria: - Previously indicated unwillingness to be contacted by email for participation in research studies |
Country | Name | City | State |
---|---|---|---|
United States | University of Pennsylvania | Philadelphia | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pennsylvania |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Participants that fail to complete study | The proportion of patients enrolled in GAMEPAD that failed to complete the study | 12 months | |
Other | Change in step count from baseline to end of intervention | Change in daily step count from baseline to the end of the GAMEPAD intervention (overall and stratified by overall GAME PAD study arm -gamification intervention versus attention control) | 16 weeks | |
Other | Change in step count from baseline to end of follow-up period | Change in daily step count from baseline to the end of follow-up (overall and stratified by overall GAMEPAD study arm -gamification intervention versus attention control) | 24 weeks | |
Other | Change in patient-reported symptom scores from baseline to end of GAMEPAD intervention | Change in patient-reported symptom scores from baseline to the end of the GAME PAD intervention (overall and stratified by overall GAMEPAD study arm). The Walking Impairment Questionnaire will be used to rate the degree of difficulty of various physical activities, ranging from 0 (unable) to 4 (no difficulty). Scores are divided by the maximum number of points and presented on a scale of 0%-100% where 0% indicates they are unable to do the activity and 100% indicates they have no difficulty. | 16 weeks | |
Other | Change in patient-reported symptom scores from baseline to end of follow-up period | Change in patient-reported symptom scores from baseline to the end of follow-up (overall and stratified by overall GAMEPAD study arm). The Walking Impairment Questionnaire will be used to rate the degree of difficulty of various physical activities, ranging from 0 (unable) to 4 (no difficulty). Scores are divided by the maximum number of points and presented on a scale of 0%-100% where 0% indicates they are unable to do the activity and 100% indicates they have no difficulty. | 24 weeks | |
Primary | Enrollment in GAMEPAD intervention study | The proportion of patients that enroll in the GAMEPAD intervention study | 6 Months |
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