Spinal Muscular Atrophy (SMA) Clinical Trials

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Virtual Targeted Rehabilitation for Patients With Spinal Muscular Atrophy: Phase 1.2: Proof-of-concept

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Spinal muscular atrophy is a genetic disorder characterized by progressive muscle weakness, severely impacting patients' motor abilities. Several disease modifying therapies have been developed to treat Spinal muscular atrophy which have led to new disease trajectories . According to standard of care guidelines, exercise programs should be designed and monitored by a physical therapist and should include exercises to improve daily life activities. Exercises should be adapted to each patient and can be prescribed with an optimal frequency in various ways. However, of patients with Spinal muscular atrophy, only 20% reported access to endurance exercises and only 6% to mixed exercises. This incompliance to standard of care guidelines is due to manpower limitation and difficulties in engaging with young and sometimes highly disabled children. Our group has been pioneering in developing the UK at-home individualised rehabilitation program. To address this challenge, the Investigators propose the development of an innovative, virtual targeted rehabilitation platform specifically designed for young patients with Spinal muscular atrophy. This technology aims to provide a patient-centric, at-home rehabilitation solution, enabling parents/caregivers to facilitate daily exercises in a more accessible and enjoyable manner. This technology would constitute the first of its kind in Spinal muscular atrophy field, involving the integration of augmented electromyography signals and soft robotic haptic devices into a gamified virtual reality environment. By increasing the frequency and quality of exercise interventions at home, this technology has the potential to significantly address the critical unmet need for consistent rehabilitation. This technology will also serve as a clinical outcome measure for continuous home-based assessments of weaker and less functional population in place of hospital-based assessments.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 6
Maximum Age: 18
Healthy Volunteers: f
View:

• Person with SMA

‣ A person living with genetically confirmed SMA aged from 12-18 years

⁃ A good understanding of English or someone who can provide a good understanding of English for me to complete the survey

⁃ A young person living with SMA from 12-15 years of age and who's caregiver/legal guardian gives consent

⁃ A young person living with SMA from 16-18 years of age who provide their own consent

∙ Caregiver/ Legal Guardian

• A caregiver (legal guardian) of child/young person living with SMA aged from 6-18 years old

• A good understanding of English or someone who can provide a good understanding of English for me to complete the survey

∙ Participant with SMA aged 6-10 years

• Genetically confirmed SMA

• A comprehensive understanding of English

• Treated with any disease-modifying therapy post-symptomatically

• Number of SMN2 copies available

• Functional status available

• Age: Participants between 6-10 years at Visit 1 (inclusion)

• Parent(s)/legal guardian(s)/caregiver(s) able to provide written informed consent and child able to provide assent prior to participation in the study

∙ Participant with SMA aged 11-15 years

• Genetically confirmed SMA

• A comprehensive understanding of English

• Treated with any disease-modifying therapy post-symptomatically

• Number of SMN2 copies available

• Functional status available

• Age: Participants between 11-15 years at Visit 1 (inclusion)

• Parent(s)/legal guardian(s)/caregiver(s) able to provide written informed consent and child able to provide assent prior to participation in the study

∙ Participant with SMA aged 16-18 years

• Genetically confirmed SMA

• A comprehensive understanding of English

• Treated with any disease-modifying therapy post-symptomatically

• Number of SMN2 copies available

• Functional status available

• Age: Participants between 16-18 years at Visit 1 (inclusion)

• Able to provide written informed consent

Locations
Other Locations
United Kingdom
Oxford University
RECRUITING
Oxford
Contact Information
Primary
Laurent Sevais, Professor
laurent.servais@paediatrics.ox.ac.uk
+44 (0)1865 618799
Backup
Charlotte Lilien, Doctor
charlotte.lilien@paediatrics.ox.ac.uk
+44 (0)1865 618799
Time Frame
Start Date: 2026-05-27
Estimated Completion Date: 2027-04
Participants
Target number of participants: 12
Treatments
No_intervention: Cohort 1(Survey)
Participants will be asked to complete and online survey with 17 questions (with subparts). The first 4 questions will establish their Spinal muscular atrophy condition and their movement levels. The remaining 13 questions will establish their exercise routines and use of technology in daily life. Followed by their preference for gaming, types of games and TV programs they enjoy. The participants will only be asked once to fill in the survey and this will be carried out at their own homes on their own.
Experimental: Cohort 2 (Testing)
Cohort 2 (Testing) will test out a basic device in a control laboratory environment to determine if further research for long term use and a at home device would be beneficial to patients and not have any adverse effects to their physical health. Participants will be ask to attend a pre-screening video to check eligibility for the study and be consented online at the meeting. Following this meeting 2 visits will be arranged at the University Biomedical engineering lab in Oxford and the participants asked to participate in using the device
Sponsors
Leads: University of Oxford

This content was sourced from clinicaltrials.gov

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