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Clinical Trials/NCT05646849
NCT05646849
Recruiting
Not Applicable

Using a Connected Application to Maintain Physical Activity After Cardiac Rehabilitation

University Hospital, Angers1 site in 1 country208 target enrollmentJanuary 12, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiac Rehabilitation
Sponsor
University Hospital, Angers
Enrollment
208
Locations
1
Primary Endpoint
To demonstrate an increase in the percentage of patients respecting at 6 months post-cardiac rehabilitation the recommendations in terms of physical activity
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

Maintaining physical activity after cardiac rehabilitation has a major role in disease progression and patient prognosis. 6 months after the cardiac rehabilitation, we find during a nursing interview that many patients do not maintain regular physical activity.

1 year after cardiac rehabilitation, between 30% and 60% of patients do not maintain the recommendations in terms of physical activity.

It is recommended to perform studies evaluating the effectiveness of new technologies in the fight against non-compliance recommendations for physical activity.

That is why, study the interest of using an application connected post-cardiac rehabilitation seems necessary to fight against dropouts in terms of physical activity.

Detailed Description

The objective is to study compliance with the recommendations, assessed by accelerometer at 6 months post-cardiac rehabilitation within two groups : classic care versus using a connected application.

Registry
clinicaltrials.gov
Start Date
January 12, 2023
End Date
July 1, 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
University Hospital, Angers
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient participating in cardiac rehabilitation
  • Patient with a smartphone compatible with the application
  • Patient with internet connection
  • Patient having signed the written consent to participate

Exclusion Criteria

  • Patient reluctant or unable to comply with the protocol
  • Pregnant, parturient and nursing mothers
  • Persons deprived of their liberty or under guardianship

Outcomes

Primary Outcomes

To demonstrate an increase in the percentage of patients respecting at 6 months post-cardiac rehabilitation the recommendations in terms of physical activity

Time Frame: at 6 months

accelerometer

Secondary Outcomes

  • to study within each group the evolution of the motivation to physical activity between the end of the cardiac rehabilitation.(at 6 months)
  • to study the difference in the motivation to physical activity at 6 months post-cardiac rehabilitation between the two groups(at 6 months)
  • to describe patient satisfaction in the intervention group(at 6 months)
  • to describe the frequency of use of patients in the intervention group to be recorded their sessions(at 6 months)
  • to describe the interactions with other users in the intervention group(at 6 months)
  • to describe participation in challenges in the intervention group(at 6 months)
  • to describe the use of the application in the intervention group(at 6 months)
  • to study the difference in the level of physical activity at 6 months post-cardiac rehabilitation between the two groups(at 6 months)
  • to study within each group the evolution of the level of physical activity between the end of the cardiac rehabilitation.(at 6 months)
  • to describe the maintenance of the physical activity of the two groups according to the seasonality following the end of the cardiac rehabilitation (winter, spring, summer, autumn).(at 6 months)
  • to describe the continued use of the application in the intervention group(at 18 months)

Study Sites (1)

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