Mucopolysaccharidoses (MPS) Clinical Trials

Find Mucopolysaccharidoses (MPS) Clinical Trials Near You

Co-design of a Physical Activity and Sedentary Behaviour Intervention for Adults With Mucopolysaccharidosis

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

Currently, treatments for mucopolysaccharidoses (MPS) are pharmacological and predominantly focus on the physical symptoms of the disease. In the general population and individuals with disabilities, increasing physical activity levels and reducing sedentary time can be an effective, non-pharmacological treatment to improve mental health and quality of life. Such interventions have not yet been developed or evaluated in people with MPS. The aim of this study is to co-design a physical activity and sedentary behaviour intervention tailored to the needs of adults with MPS. The study will seek to gain the expertise of adults with MPS, specialist stakeholders (physicians and clinical nurse specialists) and lay specialist stakeholders (family and friends of adults with MPS and members of staff and volunteers at the Society for Mucopolysaccharide Diseases). A range of views and experiences of physical activity and sedentary behaviour will be explored via focus groups (with individuals with MPS and lay specialist stakeholders) and semi-structured interviews (with specialist stakeholders). The information gathered from the focus groups and interviews will then be utilised to inform participatory workshops (with individuals with MPS) to test intervention concepts. Data from these activities will inform the design of a future intervention.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: t
View:

• Diagnosed with any type of Mucopolysaccharidosis.

• Aged ≥ 18 years old.

• Lives in the United Kingdom.

• Deemed safe to participate by a clinician (for participatory workshops).

Locations
Other Locations
United Kingdom
Brunel University London
RECRUITING
London
Contact Information
Primary
Daniel Bailey
daniel.bailey@brunel.ac.uk
01895265363
Backup
Sarah Gosling
sarah.gosling@brunel.ac.uk
01895265363
Time Frame
Start Date: 2026-03-20
Estimated Completion Date: 2026-09-30
Participants
Target number of participants: 50
Treatments
Adults with Mucopolysaccharidosis
Focus groups and participatory workshops
Lay specialist stakeholders
Focus groups
Specialist stakeholders
Interviews
Related Therapeutic Areas
Sponsors
Collaborators: Northern Care Alliance NHS Foundation Trust, Royal Free Hospital NHS Foundation Trust, University College London Hospitals
Leads: Brunel University

This content was sourced from clinicaltrials.gov