Cardiac Rehabilitation
Conditions
Keywords
Cardiac Rehabilitation
Brief summary
The goal of this study is to collect wearable sensor data that the investigators hypothesize will be useful in future algorithm development for monitoring recovering of participants enrolled in cardiac rehabilitation programs. Participants will be provided one or more smartwatches and/or smart rings to wear during a 14 week study which includes 2 weeks of baseline data collection and a 12-week, 36-session cardiac rehabilitation program. They will capture a pre-assessment 6 minute walk tests and a post-assessment 6 minute walk test. They will otherwise conduct standard cardiac rehabilitation program procedures and our sensors will capture data and sleep information throughout the study period.
Detailed description
The goal of this study is to collect wearable sensor data that the investigators hypothesize will be useful in future algorithm development for monitoring the recovery of participants enrolled in cardiac rehabilitation programs. Participants will be provided one or more smartwatches and/or smart rings to wear during a 14 week study which includes 2 weeks of baseline data collection and a 12-week, 36-session cardiac rehabilitation program. They will capture a pre-assessment 6 minute walk tests and a post-assessment 6 minute walk test. They will otherwise conduct standard cardiac rehabilitation program procedures and our sensors will capture data and sleep information throughout the study period. This work will use data from cardiac rehabilitation, captured from smartwatches, and data from rest/sleep, captured from smartwatches and smartrings, to see if there are trends in recovery that can be modeled. Recovery is measured as an improvement in 6 minute walk test performance over the course of cardiac rehabilitation.
Interventions
DEVICEWearable Sensors
Participants will wear smartwatches and smartrings and this data will be used to design algorithms which seek to find associations between device data and recovery.
Sponsors
Ascension Health
Texas A&M University
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Enrollment in Cardiac Rehabilitation - eligible all-comers to Cardiac Rehabilitation * Age 18 or older * Native English speaker
Exclusion criteria
* Inability to wear one or more SmartWatches or Smartring * Inability to walk unassisted * Inability to participate in cardiac rehabilitation * Inability to use a smartphone to aid in upload of remote data * Lack of smartphone to use in the study * There is a change in participant health such that the participant meets any of the
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Improvement in cardiac function | 12 weeks, 36 session cardiac rehabilitation | Improvement in the 6 minute walk test performance from pre assessment to post assessment |
Countries
United States
Outcome results
None listed