Novel Respiratory Training as Part of Palliative Care for Older Adults With Heart Failure
Launched by UNIVERSITY OF PITTSBURGH · Aug 26, 2024
Trial Information
Current as of June 26, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is exploring a new way to help older adults with heart failure improve their physical abilities and quality of life through a program called inspiratory muscle training (IMT). The researchers believe that older patients, aged 70 and above, can safely and effectively do this training at home for 12 weeks. They expect that participants who engage in IMT will see improvements in their ability to perform daily activities, like standing up and walking, along with better breathing, reduced fatigue, and an overall better sense of well-being compared to those who receive standard care.
To be eligible for this trial, participants need to be 70 years or older and diagnosed with advanced heart failure, which means their heart does not pump blood as well as it should. They must also be receiving appropriate heart failure treatment. However, individuals living in care facilities or those with certain serious health conditions, like severe lung disease or recent major heart events, cannot take part. Participants can expect to follow a guided training program from home, and their progress will be monitored throughout the study.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Patients with Advanced Heart Failure (HFrEF or HFpEF), with NYHA class II, III, or IV despite a minimum of
- • 6 weeks of treatment
- • Age \>70 years
- • Male and Female
- • Optimal therapy according to AHA/ACC and HFSA HF guidelines
- Exclusion Criteria:
- • Patients living in an institutional setting (e.g., skilled nursing home) during the intended period of this study.
- • Major cardiovascular event or procedure within the prior 6 weeks.
- • HF secondary to significant uncorrected primary valvular disease (except mitral regurgitation secondary to left ventricular dysfunction). If valve replacement has been performed, the participant may not be enrolled for 12 months after this procedure.
- • Dementia
- • Severe COPD (FEV1\<50%), PVD, and/or Anemia
- • End-stage malignancy
- • Severe valvular heart disease
- • Psychiatric hospitalization within the last 3 months
- • Chronic ETOH or drug dependency.
- We will exclude all of the following special populations:
- • Adults unable to consent
- • Individuals who are not yet adults (infants, children, teenagers)
- • Pregnant women
- • Prisoners
About University Of Pittsburgh
The University of Pittsburgh is a leading research institution known for its commitment to advancing medical science and improving patient care through innovative clinical trials. With a robust infrastructure for research and a multidisciplinary approach, the university fosters collaboration among experts in various fields, facilitating the development of novel therapies and interventions. Its clinical trial programs emphasize ethical standards, patient safety, and the integration of cutting-edge technology, making the University of Pittsburgh a pivotal contributor to the landscape of clinical research and a trusted partner in the pursuit of health advancements.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Pittsburgh, Pennsylvania, United States
Patients applied
Trial Officials
Daniel E. Forman, M.D
Principal Investigator
University of Pittsburgh
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported