Actively Recruiting
National Survey of Physical Activity Restrictions and Quality of Life Among Patients With Fibromuscular Dysplasia
Led by Vanderbilt University Medical Center · Updated on 2026-04-20
2000
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
Sponsors
V
Vanderbilt University Medical Center
Lead Sponsor
F
Fibromuscular Dysplasia Society of America
Collaborating Sponsor
AI-Summary
What this Trial Is About
Fibromuscular dysplasia (FMD) is a disease affecting medium-sized arteries without plaque or inflammation, mainly impacting women and middle-aged adults. Some patients with FMD may experience serious complications like heart attacks, strokes, aneurysms, or blood vessel tears. Due to these risks, many patients are advised to restrict physical activities, but there are no formal guidelines on appropriate exercise for FMD, which may affect their quality of life and cause confusion. This research is an observational national survey conducted electronically to gather information from patients diagnosed with FMD about the types of physical activity restrictions they have received and how these impact their quality of life and emotional well-being. The survey aims to collect data to support the development of expert consensus recommendations on physical activity tailored to different FMD types, which could improve patient education and empowerment. Participants will complete an electronic survey assessing clinician-recommended physical activity restrictions, self-reported changes in activity after diagnosis, and the emotional and physical effects of these recommendations. The study will measure these outcomes at baseline to understand the current impact on patients. The total participation involves completing the survey online, with no additional treatments or visits required.
CONDITIONS
Brief Title
Survey on Physical Activity and Qualify of Life in Fibromuscular Dysplasia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants with a diagnosis of fibromuscular dysplasia
- Age range = 18-100 years
You will not qualify if you...
- Inability to complete the electronic consent form or electronic survey for any reason
- Non-English speaking participants who cannot read the electronic consent form or electronic survey
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Single time point
Participants complete an electronic survey about physical activity restrictions and quality of life related to fibromuscular dysplasia.
1 electronic survey completion
Trial Site Locations
Total: 1 location
1
Vanderbilt University Medical Center
Nashville, Tennessee, United States, 37232
Actively Recruiting
Research Team
A
Amanda Morrison, MD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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