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Wearables and Cardiac Rehabilitation

Texas A&M University logo

Texas A&M University

Status

Active, not recruiting

Conditions

Cardiac Rehabilitation

Treatments

Device: Wearable Sensors

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT06065319
R21EB028486

Details and patient eligibility

About

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.

Full 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.

Enrollment

18 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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 exclusion criteria for this study during the course of the cardiac rehab sessions

Trial design

18 participants in 1 patient group

All Comers to Cardiac Rehabilitation
Description:
Any participant that is enrolled in cardiac rehabilitation is eligible for this study.
Treatment:
Device: Wearable Sensors

Trial documents
2

Trial contacts and locations

2

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Central trial contact

Bobak Mortazavi; Chloe Cowan

Data sourced from clinicaltrials.gov

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