Non-inferiority Study of a Cardiac Tele-rehabilitation in Hybrid Form Compared to a Cardiac Rehabilitation

Étude de Non-infériorité d'un Programme de télé-réadaptation Cardiovasculaire Sous Une Forme Hybride Par Rapport à Une rééducation réadaptation Cardiovasculaire Classique

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT05702216

Acronym

TELEREHAB

Enrollment

Registered

2023-01-27

Start date

2021-10-29

Completion date

2023-03-31

Last updated

2023-12-27

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

Conditions

Cardiac Tele-rehabilitation

Keywords

Cardiac tele-rehabilitation, cardiac rehabilitation

Brief summary

Cardiac tele-rehabilitation in a hybrid form can be a choise for the management of cardiovascular diseases. The aim is to increase the participation rate of patients in cardiac rehabilitation. This new form of care can be as effective as traditional care.

Detailed description

The Covid-19 pandemic has had indirect effects on the health system, particularly in the management of cardiovascular diseases. Rehabilitation centres had to adapt their operation to the recommendations of health authorities. The choice appeared to be unavoidable: tele-rehabilitation care in a hybrid form. Moreover, Many patients do not participate at this kind of care. Many identified factors can explain this low rate of participation : a lack of proximity facilities does not promote patient participation. The objective of this study is to demonstrate a comparable effectiveness between a cardiac telerehabilitation programme in hybrid form and a cardiac classic rehabilitation programme.

Interventions

OTHERRehabilitation

Hybrid approach in cardiac telerehabilitation. Patients underwent 20 cardiac rehabilitation sessions: alternatively, patients underwent 10 classical cardiac rehabilitation sessions in the clinic and 10 cardiac telerehabilitation sessions at home.

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

HEALTH_SERVICES_RESEARCH

Masking

NONE

Intervention model description

Randomization in two groups: a Hybrid Tele-pulmonary Rehabilitation group and a classic Rehabilitation group.

Eligibility

Sex/Gender

ALL

Age

18 Years to 80 Years

Healthy volunteers

Inclusion criteria

* Age ≥ 18 ans * Patients with heart disease * Inclusion in the rehabilitation program

Exclusion criteria

* Cardiac decompensation * No stabilised acute coronary syndrome * Decompensated heart failure * Severe ventricular rhythm disorders * Severe functional limitation

Design outcomes

Primary

Measure	Time frame	Description
6-minute walk test	6 weeks before baseline	Distance covered in the 6-minute walk test

Secondary

Measure	Time frame	Description
Stress test	6 weeks before baseline	12-lead electrocardiogram
Wall Squat Test	6 weeks before baseline	Muscular endurance

Countries

France

Outcome results

None listed

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