Families' Perceptions of Powered Mobility for Participation in Children With Spinal Muscular Atrophy Type 1: A Photovoice Study

Families were actively involved in multiple stages of the study, including its design, data collection and interpretation and dissemination of the results. Using the photovoice method, parents documented their children's experiences with powered mobility through photographs and comments, highlighting both benefits and challenges. Their input was crucial in identifying real-life barriers and needs, ensuring that the study reflected the authentic experiences of families navigating powered mobility. Additionally, they provided valuable insights during interviews, contributing to a deeper understanding of the emotional, social and practical impacts of the intervention. Their perspectives helped to shape the analysis and reinforce the importance of personalised mobility solutions.

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Publication Details

Journal
Health Expectations
Published
2025-05-07
DOI
https://doi.org/10.1111/hex.70278
Citations
4
Primary Topic
Neurogenetic and Muscular Disorders Research
Type
article
Field-Weighted Citation Impact
6.50

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article

Families' Perceptions of Powered Mobility for Participation in Children With Spinal Muscular Atrophy Type 1: A Photovoice Study

Egmar Longo, Cristina Díaz-López, Purificación López‐Muñoz, Helena Romay‐Barrero et al.
4 citations
Health Expectations
Neurogenetic and Muscular Disorders Research
6.50
article

Families' Perceptions of Powered Mobility for Participation in Children With Spinal Muscular Atrophy Type 1: A Photovoice Study

Egmar Longo, Cristina Díaz-López, Purificación López‐Muñoz, Helena Romay‐Barrero, Rocío Palomo‐Carrión, Soraya Pacheco‐da‐Costa, María Plasencia‐Robledo, María Coello‐Villalón
article en
4 citations

Abstract

Families were actively involved in multiple stages of the study, including its design, data collection and interpretation and dissemination of the results. Using the photovoice method, parents documented their children's experiences with powered mobility through photographs and comments, highlighting both benefits and challenges. Their input was crucial in identifying real-life barriers and needs, ensuring that the study reflected the authentic experiences of families navigating powered mobility. Additionally, they provided valuable insights during interviews, contributing to a deeper understanding of the emotional, social and practical impacts of the intervention. Their perspectives helped to shape the analysis and reinforce the importance of personalised mobility solutions.

Health ExpectationsVol. 28(3)
Universidade Federal da Paraíba (BR), Universidad de Alcalá (ES), University of Castilla-La Mancha (ES)
Fundación Alicia Koplowitz
Reduced inequalities
Openalex Percentile: Top 4%
Neurogenetic and Muscular Disorders Research
6.50
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Families' Perceptions of Powered Mobility for Participation in Children With Spinal Muscular Atrophy Type 1: A Photovoice Study — Egmar Longo, Cristina Díaz-López, et al. · Health Expectations (2025) | TGRS Research Map | TGRS