← Back to all trials
Not Yet Recruiting
NCT07697573
An Exercise and Lifestyle Programme for Adults With Vascular Ehlers-Danlos Syndrome: A Feasibility Study
Conditions: Vascular Ehlers Danlos Syndrome
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 40
Sponsor: Sheffield Hallam University
Location: Sheffield Hallam University Sheffield South Yorkshire
Summary
Vascular Ehlers-Danlos syndrome (vEDS) is a rare, life-threatening connective tissue disorder. People with vEDS have often been advised to limit physical activity, yet the safety and feasibility of structured exercise in this group is poorly understood. This study works with people with vEDS, their families and clinicians to co-design a safe, tailored physical activity programme, then tests it in a 12-week randomised feasibility study comparing the programme with usual care. The aim is to find out whether the intervention and the trial procedures are safe, acceptable and practical, in order to inform a future full-scale trial. Outcomes focus on recruitment, retention, adherence, acceptability and safety, alongside exploratory measures of physical function, quality of life and microvascular health.
Eligibility Criteria
Inclusion Criteria:
* Adults aged 18 years or older
* Confirmed diagnosis of vascular Ehlers-Danlos syndrome (vEDS)
* Living in the UK
* Able to provide informed consent
* Medically stable, defined as: no arterial dissection, rupture, or other major vEDS-related vascular event within the preceding 6 months; no recent hospitalisation for vEDS complications; and blood pressure considered controlled by their treating clinician
* Medical clearance from their treating clinician
* Not pregnant at the time of enrolment
Exclusion Criteria:
* Major vEDS-related vascular event (arterial dissection or rupture) within the previous 6 months
* Recent hospitalisation for vEDS complications
* Blood pressure not controlled by treating clinician
* Pregnancy at enrolment (participants who become pregnant during the intervention are withdrawn from the exercise component but may continue follow-up data collection if they wish)
* Unable to provide informed consent
Source: ClinicalTrials.gov (NCT07697573). StuddyBuddy aggregates publicly available trial information.