EligibleTrials

Understanding the Effects of Pulmonary Arterial Hypertension on Lean Muscle Mass

Recruiting · NCT07132788 · Observational (researchers observe without assigning treatment) · Lead sponsor: University of Pennsylvania

View the official record on ClinicalTrials.gov →
Hypertension

Interventions studied

24 hour diet recallActivity monitoringChest CT scanDual-Energy X-ray Absorptiometry ScanEchocardiogramGrip strength testInternational Physical Activity Questionnaire Short Form (IPAQ-SF)Quality of Life Questionnaire (emPHasis 10)Short Performance Physical BatterySix minute walk testblood draw

What this trial is about

Patients with pulmonary arterial hypertension (PAH) are at increased risk of muscle loss and decreased physical activity. This study will aim to (1) understand the way in which muscle loss occurs in PAH, particularly the role of fat surrounding the heart, and (2) look at the impact muscle loss has on quality of life, daily physical activity, and hospitalizations in patients with PAH. The findings from this study could help identify potentially treatable factors that may improve the overall quality of life and physical functioning of patients with PAH. Subjects will be asked to attend a baseline visit where the following will be performed: * Measure your vital signs * Undergo a research blood draw, less than 4 tablespoons * Provide a urine pregnancy test (if applicable) * Review demographics, personal history, and medical history * Review current PAH medications * Complete questionnaires on how your PAH affects you * Complete a test of physical performance * Complete a grip strength test * Undergo an echocardiogram (Echo) * Complete a six-minute walk test * Undergo a Chest CT Scan * Undergo a scan of your body composition (DXA scan) * Obtain a weight and body composition measurement on the InBody Scale Subjects will also complete activity moniotring, two 24-hour diet recalls, and participate in remote follow-up visits every 6 months

Who can take part

Age range
18 Years and older
Sex
All (male and female)
Healthy volunteers
No - a diagnosis or condition is required
Phase
Not specified
Study type
Observational (researchers observe without assigning treatment)

Inclusion criteria

Exclusion criteria

Where it is running

2 locations listed across 2 US states.

Read the full protocol, contacts and eligibility on ClinicalTrials.gov →

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