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Smart Wearable Insights to Prevent Exacerbations and Recurrence - Rehabilitation Study: SWIPER-REHAB

Imperial College London logo

Imperial College London

Status

Not yet enrolling

Conditions

Cardiovascular Diseases

Treatments

Device: Smartwatch
Device: Imperial Healthy Hearts app

Study type

Observational

Funder types

Other

Identifiers

NCT06011395
22HH7635

Details and patient eligibility

About

Aims of the study:

  • To measure the rate of completion of a digital cardiac rehabilitation programme at Imperial College Healthcare NHS Trust (ICHNT)
  • To measure the health economic impact of a digital cardiac rehabilitation programme at ICHNT

Any adult patient eligible for ICHNT cardiac rehabilitation (CR) programmes is eligible to participate. Participants will receive a commercially available smart watch and be asked to wear the device as much as possible. In addition, they will be asked to download a smartphone application called 'Imperial Healthy Hearts', which displays movement and information on heart rate, breathing and oxygen levels to both the participant and the research team (digital data). The Healthy Hearts app also allows the direct care team to provide educational materials to patients as part of their routine care.

The clinical content and structure of the CR programme is determined by the clinical CR team, and does not deviate from established local and national standards and practices.

Researchers will capture physiological data such as heart rate, respiratory rate, blood pressure (where available) and oxygen saturation (where available) via the Healthy Hearts platform. Researchers will also capture clinical information from the electronic health record, and will compare CR programme uptake and completion rates with historical data and national targets.

Enrollment

1,800 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 18 years or above
  • Able to give informed consent
  • Eligible for Cardiac Rehabilitation programme

Exclusion criteria

  • Any wrist wound, skin pathology or other feature that would prohibit the wearing of a smartwatch
  • Any visual impairment preventing the use of the Fitbit or smartphone application.

Trial contacts and locations

1

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Central trial contact

Mihir Kelshiker, MD

Data sourced from clinicaltrials.gov

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