Financial incentive
BehavioralA daily financial incentive framed as a loss of $2 each day goal is not acheived
NCT Number: NCT02531022
This study will use a randomized, controlled trial to test the effectiveness of a home-based physical activity program using wearable devices and financial incentives. All participants in will establish a baseline step count during the first two weeks and then proceed to a 16-week intervention period and 8-week follow-up period.
Looking for future studies?
Notify Me18 year and older
All sexes
Interventional
Not applicable
Cardiovascular disease is the leading cause of mortality in the United States. Among patients that survive an acute myocardial infarction (AMI), cardiac rehabilitation (CR) has been demonstrated to effectively reduce risk of re-infarction, cardiac mortality, and all-cause mortality. However, despite cardiac rehabilitation being a Class I (standard of care) recommendation in multiple American Heart Association acute myocardial infarction guidelines, more than 80% of eligible patients do not receive appropriate cardiac rehabilitation and much of this is due to challenges in access to these programs. Recent innovations in technology allow us to passively monitor an individual's physical activity using wearable devices. Incentives designed using insights from behavioral economics have been demonstrated to motivate device engagement and behavior change. A remotely-monitored cardiac rehabilitation program could improve access for many individuals and potentially be more cost-effective because it is less resource- and personnel-intensive. The objective of this study is to use a randomized, controlled trial to test the effectiveness of a home-based physical activity program using wearable devices and financial incentives.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
A daily financial incentive framed as a loss of $2 each day goal is not acheived
Daily feedback from an activity tracking device worn on the wrist to track step counts and sleep patterns
Time frame: Baseline and end of Maintenance Period at Week 16
The primary outcome variable is the change in mean daily step count from the baseline period to the maintenance period (weeks 9-16).
Time frame: Baseline and end of Follow Up Period at week 24
Secondary outcomes include change in mean daily steps from the baseline period to the follow-up period (weeks 17-24).
University of Pennsylvania
Other
A Randomized, Controlled Trial Evaluating Methods to Use Physical Activity to Improve Outcomes After Acute Coronary Syndrome
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT03234023
Acute Coronary Syndrome, Behavior
Ferrol, A Coruña, Spain
View Trial DetailsNCT07597460
Behavior, Child Health
Santiago, Chile
View Trial DetailsNCT06869369
Behavior, Motor Activity
Kütahya, Turkey (Türkiye)
View Trial DetailsNCT07729007
Behavior, Fitness
Madrid, Spain
View Trial Details