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Experiences, Outcomes and Unmet Needs of Caregivers of Children With Cerebral Palsy

NCT06912373 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 30

Last updated 2025-04-04

No results posted yet for this study

Summary

Cerebral palsy (CP ) is one of the most prevalent motor disabilities in childhood, significantly impacting both children and their caregivers. This study explores the experiences, psychological well-being, and unmet needs of caregivers of children with CP. 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 ).

Conditions

  • Cerebral Palsy Infantile
  • Caregiver

Sponsors & Collaborators

  • Universitat de Lleida

    lead OTHER

Principal Investigators

  • Francesc Valenzuela, PhD · Universitat de Lleida

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-04-01
Primary Completion
2025-06-30
Completion
2025-08-01

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06912373 on ClinicalTrials.gov