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Using a Connected Application to Maintain Physical Activity After Cardiac Rehabilitation

Using a Connected Application to Maintain Physical Activity After Cardiac Rehabilitation

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05646849
Acronym
APA&CO2
Enrollment
208
Registered
2022-12-12
Start date
2023-01-12
Completion date
2026-07-01
Last updated
2024-03-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome, Cardiac Rehabilitation, Heart Failure

Keywords

Cardiac Rehabilitation, Acute Coronary Syndrome, Heart Failure

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.

Interventions

OTHERConnected application

Recording and sharing sessions. Exchanges and interactions with other patients. Participation in three collective challenges.

Sponsors

University Hospital, Angers
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

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

Secondary

MeasureTime frameDescription
to study within each group the evolution of the motivation to physical activity between the end of the cardiac rehabilitation.at 6 monthsquestionnaire EMAPS
to study the difference in the level of physical activity at 6 months post-cardiac rehabilitation between the two groupsat 6 monthsquestionnaires IPAQ
to study the difference in the motivation to physical activity at 6 months post-cardiac rehabilitation between the two groupsat 6 monthsquestionnaire EMAPS
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 monthsaccelerometer
to describe the use of the application in the intervention groupat 6 monthsnumber of recorded sessions
to study within each group the evolution of the level of physical activity between the end of the cardiac rehabilitation.at 6 monthsquestionnaires IPAQ
to describe the frequency of use of patients in the intervention group to be recorded their sessionsat 6 monthsscale 0-4 (min 0 - max 4)
to describe the interactions with other users in the intervention groupat 6 monthsscale 0-4 (min 0 -max 4)
to describe participation in challenges in the intervention groupat 6 monthsscale 0-3 (min 0 - max 3)
to describe the continued use of the application in the intervention groupat 12 monthsnumber of recorded sessions
to describe patient satisfaction in the intervention groupat 6 monthsscale 0-10 (min 0 - max 10)

Countries

France

Contacts

Primary ContactMarie Gaume
unite-recherche-clinique@ch-cholet.fr+33241496000
Backup ContactDRCI CHU Angers
drci-promotion-interne@chu-angers.fr+33241356329

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026