CAPACITY (Cardiac Amyloidosis and Physical ACtivITY) Study
Launched by WAKE FOREST UNIVERSITY HEALTH SCIENCES · Oct 17, 2023
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
The CAPACITY Study is looking at how exercise training can help people with cardiac amyloidosis, a condition that affects the heart's ability to function properly. The trial will explore whether regular physical activity can improve fitness and overall quality of life for patients with heart failure, particularly those whose heart function is still preserved.
To participate, individuals must be at least 18 years old and have a diagnosis of heart failure that is classified as NYHA Class I-III, which means their symptoms are mild to moderate. They should be able to exercise and be on stable treatment for their condition. Participants will attend supervised exercise sessions three times a week for 12 weeks, where they will engage in activities designed to improve their heart health. It's important to note that those with advanced heart failure, breathing issues that require oxygen at home, or significant balance problems may not be eligible. This study is currently recruiting participants, and interested individuals should have a life expectancy of at least six months and be willing to follow the program guidelines.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 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
- Exclusion Criteria:
- • Inability to provide informed consent
- • Inability to commit to in-person supervised exercise sessions for three one-hour sessions a week for 12 weeks
- • NYHA Class IV Heart Failure
- • Pulmonary disease requiring home oxygen
- • Gait instability or history of prior falls
- • 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.
About Wake Forest University Health Sciences
Wake Forest University Health Sciences is a leading academic research institution dedicated to advancing healthcare through innovative clinical trials and translational research. With a strong emphasis on multidisciplinary collaboration, the organization leverages its extensive expertise in medical research, patient care, and education to develop and evaluate new therapies and interventions. Committed to improving patient outcomes and public health, Wake Forest University Health Sciences fosters a dynamic environment for scientific inquiry, engaging in a wide range of clinical studies that address pressing health challenges. Through its rigorous methodologies and ethical standards, the institution aims to contribute significantly to the medical field and enhance the quality of life for diverse populations.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Charlotte, North Carolina, United States
Patients applied
Trial Officials
Jai Singh, MD
Principal Investigator
Wake Forest University Health Sciences
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported