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.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 40 (estimated) |
| Sponsor | University Hospital, Montpellier Academic / other |
| Locations | 1 site (Montpellier) |
| Status | Recruiting |
| Started | September 23, 2026 |
| Main results expected | September 23, 2029 |
| Study ends | September 23, 2029 |
| Registry record updated | October 8, 2026 |
| Trial ID | NCT07494942 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
- Study coordinator: Susan Martinez, PhD
- Email: s-martinezjahnke@chu-montpellier.fr
- Phone: 04 67 33 52 56
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Acoramidis for ATTR-CM: Cardiac Imaging Study
This study tests whether acoramidis can improve heart structure and function in people with transthyretin amyloid cardiomyopathy.
-
SCTC21C plus bortezomib, cyclophosphamide and dexamethasone for newly diagnosed systemic light-chain (AL) amyloidosis
This trial tests whether adding SCTC21C to standard bortezomib‑cyclophosphamide‑dexamethasone (VCd) helps people with newly diagnosed AL (light‑chain) amyloidosis achieve better hematologic responses and outcomes.
-
In-home cancer treatment with remote specialist support for patients in the Florida Panhandle
This program will try giving standard cancer treatments at home to people living in the Florida Panhandle and nearby areas to see if they prefer it and have better treatment satisfaction.
-
18F‑FT8 PET imaging for light‑chain (AL) cardiac amyloidosis
This project tests whether a new PET tracer, 18F‑FT8, can safely and clearly image light‑chain (AL) cardiac amyloidosis in adults with suspected or known disease and in healthy volunteers.
-
Belantamab Mafodotin with a chemotherapy combo for newly diagnosed AL amyloidosis
This study tests whether adding belantamab mafodotin to a regimen of cyclophosphamide, bortezomib, and dexamethasone can help adults with newly diagnosed AL amyloidosis.
-
Magnetocardiography for Cardiac Amyloidosis
This project tests whether magnetocardiography (MCG) can help diagnose and monitor heart involvement in adults with amyloidosis compared with ECG and other standard tests.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.