Family Involvement and at-Home Physical Therapy on Duchenne Muscular Dystrophy: A Randomized Controlled Trial
Metadatos
Mostrar el registro completo del ítemAutor
Hernández Sánchez, Andrea; Parra-Sánchez, Lidia; Montolio, Marisol; Rueda-Ruzafa, Lola; Ortiz-Comino, Lucía; Sánchez-Joya, María del MarEditorial
Elsevier
Materia
Children Duchenne Muscular Dystrophy Family Involvement Motor Function Physical Therapy
Fecha
2024-03Referencia bibliográfica
Hernández-Sánchez A, Parra-Sánchez L, Montolio M, Rueda-Ruzafa L, Ortiz-Comino L, Sánchez-Joya MDM. Family Involvement and at-Home Physical Therapy on Duchenne Muscular Dystrophy: A Randomized Controlled Trial. Pediatr Neurol. 2024 Mar;152:34-40. doi: 10.1016/j.pediatrneurol.2023.12.015. Epub 2023 Dec 22. PMID: 38184986.
Resumen
Background: Duchenne muscular dystrophy (DMD) is a genetic condition that causes muscle weakness and begins in early childhood. To treat its complications, the rehabilitation program includes physical therapy, mainly on the musculoskeletal and the respiratory complications that appear on the evolution of the disease. This study aims to explore the effects of physical therapy with or without an at-home program on motor function among children with DMD.
Methods: A randomized controlled trial was carried out for one year (one group with at-home and conventional physical therapy and another with conventional physical therapy). Motor function was measured using the Motor Function Measure (MFM) scale, the Vignos and Brooke scales, the Timed-up-and-Go test, and the six-minute walk distance test.
Results: Twenty-seven participants with DMD participated in this study. In the at-home and conventional physical therapy group, better motor function at the distal and global level was maintained, per the results of the MFM scale (P < 0.05). The rest of the variables did not achieve statistically significant changes.
Conclusions: Our results suggest that complementing conventional treatment with at-home treatment in which the family is involved maintains better motor function, in participants with DMD