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NCT05292287Completed

Remote Maintenance Cardiac Rehabilitation

Remote Maintenance Cardiac Rehabilitation: a Randomised Feasibility Study

Source: ClinicalTrials.gov · Last updated 20 Aug 2024

Brief summary (registry, in English)

The investigators would like to test the feasibility of a remotely prescribed and monitored exercise program in people with coronary heart disease, using a wearable activity device and text message support, compared to usual care after completing cardiac rehabilitation. One group will use a Polar Ignite watch to guide them through exercise sessions at home and will receive text message feedback. The other group will be asked to continue their routine as usual. Assessments of both groups will happen after the completion of cardiac rehabilitation and at three follow-up time points of three, six, and twelve months. The aim of these treatments is to see if the investigators can help people to maintain their exercise adherence and coronary heart disease risk factor management after completing cardiac rehabilitation.

Status (registry)
Completed
Study type
Interventional
Enrollment
30 (actual)
First submitted
16 Dec 2021
Start date
28 Mar 2022
Primary completion date
15 Feb 2024
Lead sponsor
Coventry University
NCT number
NCT05292287

What you commit to

  • Study type: Interventional
  • Participants enrolled: 30
  • From 28 Mar 2022 to the primary completion date, 15 Feb 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Diagnosed atrial fibrillation or other arrhythmia preventing accurate heart rate measurement.
  • Allergy to watch materials.

Other

  • Absolute contraindications to exercise as per international clinical guidelines.
  • Any serious mental health/cognitive issue that will prevent engagement with study procedures or increase the risk of exercise complications.

Who the study is looking for

  • Diagnosed coronary heart disease.
  • Completed community cardiac rehabilitation.
  • Clinically stable (symptoms and medication).
  • Men and women aged over 18.
  • Access to smartphone with Bluetooth capacity or a computer/laptop.
  • Able to provide informed consent.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Atrium Health Limited
Coordinator of this site? Confirm its status
CoventryUnited KingdomUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.