Home Rehabilitation Improves Cardiac Effort in Pulmonary Arterial Hypertension

What this study is about

The purpose of this study is to evaluate whether a home rehabilitation program for patients diagnosed with Pulmonary Arterial Hypertension (PAH) will decrease Cardiac Effort (number of heart beats used during 6-minute walk test/walk distance) and improve quality of life. Ultimately, this information could help improve the management of patients with PAH.

Who can join (things the study team will check)

✅ You may be able to join if…

• Follows at University of Rochester Medical Center Pulmonary Hypertension Clinic.
• Adult patients (\>18 years old) with right heart catheterization confirmed pulmonary hypertension (PAH) on stable vasodilator dosing for at least 30 days. No planned titrations will occur during the 12-week study. If during the study, the treating physician feels it is necessary for safety reasons to adjust dosing, the subject will remain in their assigned group.
• Access to a smart phone or email to receive daily messages. If patients do not have access to either, we will offer a smartphone with cellular service for use during the study to receive daily messages.
• Clinically stable by the investigator (i.e., we will not enroll patients who endorse ongoing improvement or clinical worsening at enrollment).
• The treating investigator (Dr. Lachant or Dr. White) will review the clinical data of an eligible patient and establish them as safe to participate prior to approaching the patient for enrollment (i.e. not in decompensated heart failure or with recurrent pre-syncopal episodes prior to enrollment).

🚫 You may not be able to join if…

• Pregnancy.
• Pulmonary Hypertension Groups 2-5.
• Resting tachycardia \>120 beats/m during screening.
• Inability to walk.
• WHO Functional Class IV
• Lack of access to email or text messaging.
• Inability to follow daily instructions. including the two home 6-minute walk tests during the initial monitoring period. This is to show compliance with the protocol.
• Participating in a self-reported rehabilitation or exercise program.
• Oxygen therapy of more than 6 L/min at rest.
• Principal Investigator discretion

Where this trial is running

• University of Rochester Medical Center, Rochester, New York, United States

Who to contact

Daniel Lachant, DO · 585-273-4608 · daniel_lachant@urmc.rochester.edu

It's completely normal to call and ask questions before deciding anything. Mention the study ID: NCT06477640.