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NCT06222762Recruiting

Effect of Personalized Follow-up in Adapted Physical Activities in Subjects With Chronic Heart Failure.

Effect of a Personalized Follow-up in Adapted Physical Activities on the Long-term Benefits of Rehabilitation in Subjects With Chronic Heart Failure.

Source: ClinicalTrials.gov · Last updated 26 Jun 2026

Brief summary (registry, in English)

France has one million people with heart failure (HF). Exercise intolerance, characterised by dyspnoea, is the main clinical symptom in HF patients and a key determinant of reduced quality of life. In addition to drug and surgical treatments, cardiac rehabilitation programmes have shown benefits in heart failure patients. Lasting at least 3 weeks, these programmes improve physical abilities, quality of life and reduce the risk of hospitalisation for heart failure patients. To date, the real challenge is no longer to prove the benefits of cardiac rehabilitation, but to find solutions to maintain its long-term effects. The transition between the end of the supervised programmes in the centre and the return home is a difficult phase for the majority of patients who do not continue regular physical activity and thus quickly lose the benefits of the programme. To help maintain the benefits of cardiac rehabilitation, some centres offer patients programmes to continue physical activity during phase III. Although these options are often beneficial in the first few months after the end of rehabilitation compared to control groups, the long-term results are mixed. These results imply that one of these maintenance options may not be suitable for all patients. It is therefore important to propose a personalised post-rehabilitation follow-up involving the patient in the choice of physical activities to optimise the maintenance of long-term benefits. We hypothesise that patients who receive personalised support from a sport and health professional following rehabilitation maintain long-term benefits compared to a control group who do not receive this support.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
90 (estimated)
First submitted
26 Oct 2023
Start date
13 Feb 2024
Primary completion date
13 Sept 2027
Lead sponsor
University Hospital, Brest
NCT number
NCT06222762

What you commit to

  • Study type: Interventional
  • Planned participants: 90
  • From 13 Feb 2024 to the primary completion date, 13 Sept 2027
  • 2 sites 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.

Age

  • Subjects over 80 years of age at the time of inclusion

Other

  • Patient refusal
  • Minor patients
  • Subjects under guardianship or curatorship

Who the study is looking for

  • Diagnosis of stable heart failure with NYHA stage I, II or III
  • Participation in a cardiac rehabilitation programme
  • Patient agreement
  • Patient of legal age
  • Patient affiliated to the Social Security

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

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

SiteCityCountrySite status
CHU de Brest
Coordinator of this site? Confirm its status
BrestFranceRecruiting
Fondation ILDYS
Coordinator of this site? Confirm its status
BrestFranceRecruiting

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