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NCT06096675Recruiting

CAPACITY (Cardiac Amyloidosis and Physical ACtivITY) Study

Pilot Study Evaluating Supervised Cardiac Rehabilitation in Patients With Cardiac Amyloidosis

Source: ClinicalTrials.gov · Last updated 21 Jul 2026

Brief summary (registry, in English)

Exercise training in patients with heart failure and preserved ejection fraction (HFpEF) has been associated with an improvement in cardiorespiratory fitness and quality of life.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
50 (estimated)
First submitted
17 Oct 2023
Start date
22 Jan 2024
Primary completion date
Dec 2027
Lead sponsor
Wake Forest University Health Sciences
NCT number
NCT06096675

What you commit to

  • Study type: Interventional
  • Planned participants: 50
  • From 22 Jan 2024 to the primary completion date, Dec 2027
  • 1 site 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.

Prior treatment

  • Gait instability or history of prior falls

Other illness

  • NYHA Class IV Heart Failure
  • Pulmonary disease requiring home oxygen
  • In the opinion of the Principal Investigator, have a clinically significant comorbid disease that is likely to affect the ability of the patient to complete the trial, interfere with their ability with measurement of self-reported outcomes.

Other

  • Inability to provide informed consent
  • Inability to commit to in-person supervised exercise sessions for three one-hour sessions a week for 12 weeks

Who the study is looking for

  • Age \> 18
  • New York Heart Association (NYHA) Class I-III Heart Failure
  • Able to Exercise
  • On stable treatment for their cardiac amyloidosis or under active surveillance
  • Life expectancy of at least 6 months
  • Ability to understand and the willingness to sign a written informed consent document in English, and the willingness/ability to comply with the protocol activities
  • Participant must be able and willing to follow the cardiac rehabilitation activities

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

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Sanger Heart and Vascular Institute
Coordinator of this site? Confirm its status
CharlotteUnited StatesRecruiting

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