# Experiences, outcomes and unmet needs of caregivers of children with Cerebral Palsy in Spain: Protocol for a mixed-methods study

**Authors:** Clàudia Arumí-Trujillo, Francisco José Verdejo-Amengual, Oriol Martínez-Navarro, Jord J.T. Vink, Fran Valenzuela-Pascual

PMC · DOI: 10.1371/journal.pone.0342763 · PLOS One · 2026-03-13

## TL;DR

This study examines the challenges and needs of caregivers of children with Cerebral Palsy in Spain using both surveys and interviews.

## Contribution

The study introduces a mixed-methods approach to understand caregiver experiences and unmet needs in the context of Cerebral Palsy in Spain.

## Key findings

- Caregivers report high stress and low quality of life due to their child's condition and lack of support.
- The study will provide insights into the need for family-centered interventions and better healthcare policies.
- Combining quantitative and qualitative data will offer a comprehensive view of caregiving challenges.

## Abstract

Cerebral Palsy is one of the most prevalent motor disabilities in childhood, significantly impacting both children and their caregivers. This mixed-methods study explores the experiences, psychological well-being, and unmet needs of caregivers of children with Cerebral Palsy. Using an explanatory sequential design (QUAN → QUAL), first it will be assessed burden, stress levels, and quality of life of caregivers through standardized questionnaires (PedsQL-FIM, ZBI, PSS-14). In the second phase, semi-structured interviews will be conducted to provide a deeper understanding of these variables. Other studies indicate that caregivers experience heightened stress and decreased quality of life, influenced by their child’s functional limitations and the lack of adequate social and healthcare support. Moreover, many caregivers struggle with navigating medical systems, balancing personal and professional responsibilities, and managing emotional distress. This study will highlight the urgent need for family-centered interventions, psychosocial support, and healthcare policies that address not only the medical needs of children with Cerebral Palsy but also the well-being of their caregivers. By integrating quantitative and qualitative data, this research will provide comprehensive insights into the caregiving burden and will offer recommendations for improving caregiver support strategies. The Clinical Trial is registered at ClinicalTrials.org with the registration number NCT06912373.

## Linked entities

- **Diseases:** Cerebral Palsy (MONDO:0006497)

## Full-text entities

- **Genes:** PSS (Potocki-Shaffer syndrome) [NCBI Gene 780904]
- **Diseases:** anxiety (MESH:D001007), Neurological disorders (MESH:D009461), disability (MESH:D009069), Cerebral Palsy (MESH:D002547), Stress (MESH:D000079225), Neurological diseases (MESH:D020271), behavioural disorders (MESH:D001523), developmental disabilities (MESH:D002658)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12987472/full.md

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Source: https://tomesphere.com/paper/PMC12987472