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RecruitingNCT07529691Updated Apr 20, 2026

Survey on Physical Activity and Qualify of Life in Fibromuscular Dysplasia

An observational study in Fibromuscular Dysplasia of Arteries, Fibromuscular Dysplasia and Spontaneous Coronary Artery Dissection, sponsored by Vanderbilt University Medical Center. Recruiting at 1 site in United States. Open to participants aged 18 Years to 100 Years. Per ClinicalTrials.gov, last updated 2026-04-20.

Sponsored by Vanderbilt University Medical Center · Observational

From the registry’s dates

  • Started Apr 2026; still recruiting 5 months later.
Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
2,000
Ages
18 Years to 100 Years
Sex
All
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Study summary

Fibromuscular dysplasia (FMD) is a disease of the arteries that is not due to plaque build-up or inflammation. While some patients with FMD are health, some may experience heart attacks, strokes, aneurysms or blood vessel dissection/tearing which can be life-threatening. It predominantly impacts women and younger patients. As a result of this diagnosis, many patients are counseled to restrict or avoid certain physical activities out of concern for provoking or worsening vascular complications. There are no guidelines or consensus recommendations regarding appropriate physical activity for patients with FMD. The lack of consensus may lead to confusion for patients and may negatively impact their quality of life. This study will conduct a large, national survey of patients with FMD to assess the type of physical activity restrictions and impact on quality of life and emotional well-being.

Read the detailed description

Fibromuscular dysplasia (FMD) is a non-atherosclerotic, non-inflammatory disease of medium-sized arteries characterized by intimal and medial hyperplasia. The exact prevalence of FMD is unknown, but it predominantly impacts women and middle-age patients, with a mean age of 52 at the time of diagnosis. The manifestations of FMD are variable and may include spontaneous coronary artery dissection (SCAD) as well as extra-coronary vascular abnormalities (EVAs), such as peripheral artery aneurysms or dissections. Many patients are counseled to restrict or avoid certain physical activities out of concern for provoking or worsening vascular complications.3,4 However, there are no guidelines or consensus recommendations regarding appropriate physical activity for patients with FMD in the available 2018 American Heart Association (AHA) Scientific statement or the 2019 first international consensus document on FMD. Recommendations are formed based on expert opinion, and may vary based on a variety of factors including severity of disease, treating institution, or sex. The lack of consensus may lead to confusion for patients and may negatively impact their quality of life. This survey will be delivered electronically via RedCap to participants who self-identify as having a diagnosis of fibromuscular dysplasia. It will be the first to identify the breadth and content, as well as the impact, of physical activity recommendations provided by healthcare personnel to patients with FMD. Data gathered from this study will encourage the creation of an expert consensus document on recommendations for physical activity by FMD phenotype, which will have implications for patient education and empowerment for those living with FMD. This may also lead to areas of future intervention to mitigate adverse quality of life if identified.

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Conditions studied

  • Fibromuscular Dysplasia of Arteries
  • Fibromuscular Dysplasia
  • Spontaneous Coronary Artery Dissection

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Keywords

  • FMD
  • Fibromuscular dysplasia
  • SCAD
  • Exercise
  • Quality of life
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In context

Motor Activity

2,426 studies on the registry are indexed under Motor Activity; 1,161 are open to participants now.

This study's planned enrollment of 2,000 is above the median of 100 across 292 observational studies indexed under Motor Activity.

Browse Motor Activity studies →

Lead sponsor

Vanderbilt University Medical Center is the lead sponsor of 824 studies on the registry; 164 are open to participants now.

Of its 122 completed or terminated interventional studies of FDA-regulated products, 91 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 100 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Individuals with a diagnosis of fibromuscular dysplasia

Inclusion criteria

  • Participants with a diagnosis of fibromuscular dysplasia
  • Age range = 18-100 years

Exclusion criteria

Exclusion Criteria:

  • Subjects who have an inability to complete the electronic consent form or electronic survey for any reason
  • Subjects who are non-English speaking who cannot read the electronic consent form or electronic survey
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Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
2,000 participants (estimated)
Patient registry
No

Groups and cohorts

  • Patients with fibromuscular dysplasia

    Patients who identify as having a confirmed diagnosis of fibromuscular dysplasia, or patients at Vanderbilt University Medical Center who have a confirmed diagnosis of fibromuscular dysplasia as determined by their provider.

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What researchers measure

Primary outcomes

  1. Clinician-Recommended Physical Activity Restrictions

    Prevalence and type of clinician-recommended physical activity restrictions among patients diagnosed with fibromuscular dysplasia (FMD), including aerobic, resistance, and activity-specific limitations.

    Time frame: Baseline

Secondary outcomes

  1. Self-Reported Change in Physical Activity Following Diagnosis

    Change in physical activity behavior following FMD diagnosis based on patient self-report.

    Time frame: Baseline

  2. Emotional Impact of Physical Activity Recommendations

    Self-reported anxiety or depression to physical activity recommendations and/or disease-related limitations.

    Time frame: Baseline

  3. Physical Impact of Activity Recommendations

    Self-reported physical consequences (e.g. weight gain, sedentary lifestyle) associated with modification of activity level following FMD diagnosis.

    Time frame: Baseline

07

Study locations

1 of 1 sites recruiting
  • Vanderbilt University Medical Center
    Nashville, Tennessee 37232, United States
    Recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07529691
Lead sponsor
Vanderbilt University Medical Center
Collaborators
Fibromuscular Dysplasia Society of America
Responsible party
Amanda Morrison (Cardiovascular Medicine Fellow, Vanderbilt University Medical Center) — Principal investigator
First posted
Apr 14, 2026
Start date
Apr 14, 2026
Primary completion
Apr 30, 2027 (estimated)
Completion
Jun 30, 2027 (estimated)
Last update
Apr 20, 2026

Study contacts

Amanda Morrison, MD
Contact
amanda.morrison@vumc.org
615-322-5000
Aaron W Aday, MD, MSc
study chair · Vanderbilt University Medical Center

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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