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Tests a structured exercise rehabilitation program in adults with cardiac amyloidosis

Tests a 5-week exercise rehabilitation program in adults with heart amyloidosis.

Plain-language title generated from the registry record
Registry title: Impact of a Cardiac Rehabilitation Program on Patients With Cardiac Amyloidosis

Key facts

Where
Montpellier, FranceSee the site

Where in France

  • KRIEFMontpellier, FranceTaking people

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Trial details

Who runs it
University Hospital, Montpellier
Trial code
NCT07494942
Record updated
8 October 2026
Original description
The goal of this clinical trial is to learn if a structured cardiac rehabilitation program can help people with cardiac amyloidosis improve their ability to exercise and their quality of life. The main questions it aims to answer are:Read full original descriptionShow less

Impact of a Cardiac Rehabilitation Program on Patients With Cardiac Amyloidosis

The goal of this clinical trial is to learn if a structured cardiac rehabilitation program can help people with cardiac amyloidosis improve their ability to exercise and their quality of life. The main questions it aims to answer are:

Does cardiac rehabilitation raise peak oxygen uptake (VO₂ peak), which shows how well the heart and lungs work during exercise? Is cardiac rehabilitation safe and practical for people with cardiac amyloidosis? How does cardiac rehabilitation affect other exercise measures, heart function, symptoms linked to autonomic dysfunction, and quality of life?

This study has no comparison group. Researchers will measure each participant's results before and after the rehabilitation program.

Participants will:

Complete a cardiac rehabilitation program for 5 weeks. Have tests before the program starts and again about 3 months later. These tests include:

A cardiopulmonary exercise test A heart function test using electrical impedance A questionnaire about quality of life A blood sample A blood pressure test to check for orthostatic hypotension

The study will include adults aged 18 or older with transthyretin cardiac amyloidosis who are able to perform an exercise test.

Inclusion: 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: 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.

ClinicalTrials.gov NCT07494942