A Registry Based Randomized-Controlled Trial of an Upper Limb Exergaming Intervention for Children and Adolescents with Spinal Muscular Atrophy
Spinal Muscular AtrophyThis is a multisite randomized controlled registry-based trial to evaluate the efficacy of an 8-week home-based exergaming intervention as compared to usual care on occupational satisfaction of children and youth (8-18 years old age) with spinal muscular atrophy (SMA).
null
Conditions de participation
-
Sexe:
ALL -
Âges admissibles:
8 to 18
Critères de participation
Inclusion Criteria:
* Confirmed genetic diagnosis of 5q SMA
* Age at screening: Aged 8-18 years old
* Participant is able to stay seated independently without support for at least 10 seconds
* Participants has a score of at least 2 points in entry item A of the RULM (i.e., "Can raise 1 or 2 hands to the mouth but cannot raise a 200 g weight in it to the mouth")
* Treated with disease-modifying therapy
* Signed ICF
Exclusion Criteria:
* Inability to comply with study procedures according to the site investigator, prior to randomization
* Severe scoliosis or contractures that would interfere with gameplay or with successful completion of functional assessments, as confirmed by the clinical evaluator
* Planned orthopedic surgery 6 months prior to or throughout intervention and follow-up period (16 weeks post randomization)
* Inability to read in English or French
Lieu de l'étude
Hospital for SickKids
Hospital for SickKidsToronto, Ontario
Canada
Contactez l'équipe d'étude
Hernan Gonorazky
IWK Health Services
IWK Health ServicesHalifax, Nova Scotia
Canada
Contactez l'équipe d'étude
Jordan Sheriko
Alberta Children's Hospital
Alberta Children's HospitalCalgary, Alberta
Canada
Contactez l'équipe d'étude
Jean Mah
Centre de readaptation Marie-Enfant
Centre de readaptation Marie-EnfantMontreal, Quebec
Canada
Contactez l'équipe d'étude
Danielle Levac
BC Children's Hospital
BC Children's HospitalVancouver, British Columbia
Canada
Contactez l'équipe d'étude
Kathryn Selby
- Étude parrainée par
- McGill University Health Centre/Research Institute of the McGill University Health Centre
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT06396325