Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Heart-Healthy Rehab for Cardiac Amyloidosis

Official title: Impact of a Cardiac Rehabilitation Program on Patients With Cardiac Amyloidosis

Run by University Hospital, Montpellier · NCT07494942 · Data updated 2026-11-12

This study tests whether a 5-week supervised cardiac rehabilitation program can help people with cardiac amyloidosis improve exercise capacity and quality of life.

More Amyloidosis trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment40 (estimated)
SponsorUniversity Hospital, Montpellier
Academic / other
Locations1 site (Montpellier)
StatusRecruiting
StartedSeptember 23, 2026
Main results expectedSeptember 23, 2029
Study endsSeptember 23, 2029
Registry record updatedOctober 8, 2026
Trial IDNCT07494942 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults 18+ with cardiac ATTR amyloidosis who can complete a 5-week rehabilitation program and stress test.

Probably not a fit

Patients who cannot participate in a structured rehab program or who have contraindications to exercise may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Researchers will enroll adults with cardiac ATTR amyloidosis and have them complete a 5-week, daily rehabilitation program with aerobic and strength training. Before starting and about three months after completion, participants will undergo a cardiopulmonary exercise test, a non-invasive heart function assessment, and quality-of-life questionnaires to measure changes. The study uses a single-group design, comparing results within each participant from baseline to follow-up. The goal is to see if the program is feasible, safe, and beneficial for functional ability and life impact in this population. Conducted at an expert center in Montpellier, the study relies on a multidisciplinary team and standardized testing to evaluate outcomes.

Why it matters

Potential benefit: If successful, participants may experience improved exercise capacity and better quality of life.

How similar studies have gone: Previous small or heterogeneous studies in this area show potential benefits, but there is limited prospective evidence in France.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Age 18 or older
* Cardiac ATTR amyloidosis diagnosed according to guidelines: Perugini grade II or III uptake on bone scintigraphy, without monoclonal gammopathy.
* Ability to undergo a stress test
* Available to complete the 5-week rehabilitation program within 30 days of the stress test

Exclusion Criteria:

* Uncontrolled ventricular arrhythmias
* NYHA Class IV heart failure
* Inability to give informed consent to participate in the study
* Inability to monitor the patient during the study period
* Subject not enrolled in a social security program or not eligible for such a program
* Pregnant or breastfeeding women, patients unable to give consent, protected adults, vulnerable persons
* Subjects deprived of liberty by judicial or administrative decision

Where it's running

  • Krief
    Montpellier, France
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.