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- Registre américain des essais cliniques
- Essai clinique NCT07697573
An Exercise and Lifestyle Programme for Adults With Vascular Ehlers-Danlos Syndrome: A Feasibility Study
9 juillet 2026 mis à jour par: Markos Klonizakis, Sheffield Hallam University
Co-Producing and Piloting an Exercise-Based Lifestyle Intervention for Individuals With Vascular Ehlers-Danlos Syndrome (vEDS): A Mixed-Methods Feasibility Study
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.
Aperçu de l'étude
Statut
Pas encore de recrutement
Les conditions
Intervention / Traitement
Description détaillée
This is a mixed-methods feasibility study delivered across four phases.
Phase 1 uses qualitative interviews with people with vEDS, family members and clinicians to understand experiences of physical activity and decision-making under uncertain clinical guidance.
Phase 2 uses co-production focus groups to design the exercise-based lifestyle intervention.
Phase 3 is a 12-week randomised feasibility trial in which adults with vEDS are randomised to the co-produced intervention or to usual care, assessing feasibility outcomes (recruitment, retention, adherence, data completeness, acceptability and safety) and exploratory clinical measures.
Phase 4 uses post-intervention interviews to explore participant experiences and refine the intervention.
The registered trial corresponds to the Phase 3 randomised feasibility component; the qualitative phases provide the development and evaluation context.
Type d'étude
Interventionnel
Inscription (Estimé)
40
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Coordonnées de l'étude
- Nom: Ian Thistlewood
- Numéro de téléphone: +447939953194
- E-mail: i.thistlewood@shu.ac.uk
Sauvegarde des contacts de l'étude
- Nom: Markos Klonizakis
- E-mail: m.klonizakis@shu.ac.uk
Lieux d'étude
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South Yorkshire
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Sheffield, South Yorkshire, Royaume-Uni, S10 2BP
- Sheffield Hallam University
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Contact:
- Markos Klonizakis
- E-mail: m.klonizakis@shu.ac.uk
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Contact:
- Ian Thistlewood
- Numéro de téléphone: 07939953194
- E-mail: i.thistlewood@shu.ac.uk
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-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Non
La description
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
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Autre
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: Intervention
Participants receive a 12-week co-produced, remotely supervised, low-intensity and low-impact exercise-based lifestyle intervention, tailored to individual capacity, with weekly remote monitoring.
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A 12-week individually tailored exercise-based lifestyle programme, co-produced with people with vEDS, delivered remotely with supervision and weekly monitoring.
Comprises low-intensity, low-impact aerobic and functional activity progressed to individual capacity, with behavioural support to encourage sustained physical activity.
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Aucune intervention: Usual Care
Participants continue standard NHS medical care and any lifestyle advice from their treating clinicians, with no study intervention.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Recruitment rate
Délai: From study start through completion of recruitment, up to 12 months
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Proportion of eligible participants who consent to take part, expressed as a monthly recruitment rate.
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From study start through completion of recruitment, up to 12 months
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Retention rate
Délai: 12 weeks
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Proportion of randomised participants completing the 12-week intervention (progression target ≥80%)
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12 weeks
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Adherence
Délai: Over the 12-week intervention period
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Proportion of prescribed exercise sessions completed (target ≥60%), assessed by session completion records and device-based monitoring (step count and heart rate via ActiGraph accelerometer
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Over the 12-week intervention period
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Data completeness
Délai: Baseline and 12 weeks
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Proportion of participants completing outcome measures at baseline and 12 weeks (target ≥75%)
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Baseline and 12 weeks
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Acceptability
Délai: 12 weeks
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Acceptability assessed via a questionnaire informed by the Theoretical Framework of Acceptability (seven constructs, 5-point Likert scale), supplemented by post-intervention interviews
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12 weeks
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Adverse events and serious adverse events
Délai: Throughout the 12-week intervention period
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Number, type and severity of adverse events and serious adverse events, reviewed by the independent Data Safety Committee.
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Throughout the 12-week intervention period
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Fatigue
Délai: Baseline and 12 weeks
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FACIT-Fatigue Scale (Functional Assessment of Chronic Illness Therapy - Fatigue); score range 0-52; higher scores indicate less fatigue (better outcome)
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Baseline and 12 weeks
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Anxiety and depression
Délai: Baseline and 12 weeks
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Hospital Anxiety and Depression Scale (HADS); two subscales (anxiety and depression), each scored 0-21; higher scores indicate greater symptom severity (worse outcome)
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Baseline and 12 weeks
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Health-related quality of life
Délai: Baseline and 12 weeks
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EQ-5D-5L; index value ranging from below 0 to 1, where 1 = full health and higher = better; includes a 0-100 visual analogue scale (higher = better health)
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Baseline and 12 weeks
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Physical activity
Délai: Baseline and 12 weeks
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International Physical Activity Questionnaire - Short Form; reported as MET-minutes per week; higher values indicate greater physical activity
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Baseline and 12 weeks
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Lower-limb strength and endurance
Délai: Baseline and 12 weeks
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30-Second Sit-to-Stand Test; number of full sit-to-stand repetitions completed in 30 seconds; higher counts indicate better lower-limb strength and endurance (better outcome)
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Baseline and 12 weeks
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Sub-maximal aerobic capacity
Délai: Baseline and 12 weeks
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2-Minute Step Test; total number of steps completed in 2 minutes; higher counts indicate better aerobic capacity (better outcome).
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Baseline and 12 weeks
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Muscle strength
Délai: Baseline and 12 weeks
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Hand grip strength via Jamar handheld dynamometer, recorded in kilograms (best of three attempts per hand); higher values indicate greater muscle strength (better outcome)
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Baseline and 12 weeks
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Functional mobility
Délai: Baseline and 12 weeks
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Short Physical Performance Battery (SPPB); composite score 0-12 from balance, 4-metre gait speed, and 5-repetition sit-to-stand; higher scores indicate better lower-extremity function (better outcome)
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Baseline and 12 weeks
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Orthostatic heart rate response
Délai: Baseline and 12 weeks
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Heart rate measured supine and on standing (1, 3, 5 min) to screen for orthostatic intolerance
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Baseline and 12 weeks
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Orthostatic blood pressure response
Délai: Baseline and 12 weeks
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Blood pressure measured supine and on standing (1, 3, 5 min) to screen for orthostatic hypotension.
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Baseline and 12 weeks
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Microvascular function
Délai: Baseline and 12 weeks
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Cutaneous vascular conductance via Laser Speckle Contrast Imaging during local thermal hyperaemia.
Expressed as cutaneous vascular conductance (perfusion units/mmHg); higher values indicate greater microvascular reactivity
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Baseline and 12 weeks
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Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Les enquêteurs
- Chercheur principal: Markos Klonizakis, Sheffield Hallam University
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Estimé)
1 mars 2027
Achèvement primaire (Estimé)
1 octobre 2027
Achèvement de l'étude (Estimé)
17 mars 2028
Dates d'inscription aux études
Première soumission
16 juin 2026
Première soumission répondant aux critères de contrôle qualité
9 juillet 2026
Première publication (Réel)
13 juillet 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
13 juillet 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
9 juillet 2026
Dernière vérification
1 juillet 2026
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
- Dissection, vaisseau sanguin
- Maladies vasculaires
- Maladies cardiovasculaires
- Processus pathologiques
- Attributs de la maladie
- Maladies génétiques, innées
- Maladies hématologiques
- Maladies de la peau
- Anomalies congénitales
- Troubles hémostatiques
- Troubles hémorragiques
- Maladies de la peau, Génétique
- Anomalies cutanées
- Anévrisme
- Maladies du collagène
- Dissection de l'aorte
- Maladies et anomalies congénitales, héréditaires et néonatales
- Conditions pathologiques, signes et symptômes
- Comportement
- Maladies de la peau et du tissu conjonctif
- Maladies hémiques et lymphatiques
- Syndrome d'Ehlers-Danlos
- Syndrome d'Ehlers-Danlos, type IV
- Maladies rares
- Maladies du tissu conjonctif
- Activité motrice
Autres numéros d'identification d'étude
- IRAS361077
- 26/NE/0025 (Autre identifiant: REC)
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Description du régime IPD
This is a small feasibility study not powered for efficacy.
Individual participant data will not be shared.
Sheffield Hallam University is the Data Controller; data are pseudonymised, stored securely, and retained in line with UK GDPR and institutional policy.
Aggregate findings will be disseminated through open-access publication.
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Non
Étudie un produit d'appareil réglementé par la FDA américaine
Non
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .