Медицинская библиотека · Movement disorders clinical practice · 2025

A Short Version of Carers' Quality of Life Questionnaire for Parkinsonism: Data from Progressive Supranuclear Palsy Network.

Cappiello Arianna, Calandra-Buonaura Giovanna, Ceravolo Roberto, Coralli Saverio, Cuoco Sofia, Del Prete Eleonora, di Biasio Francesca, Frosini Daniela, Gualtieri Vittorio, Mascioli Davide, Sambati Luisa, Schirinzi Tommaso, Stefani Alessandro, Umbertini Elisa, Aiello Marco, Costanzo Matteo, de Micco Rosa, Fabbrini Giovanni, Failla Gaetano, Longo Chiara, Malaguti Maria Chiara, Modugno Nicola, Olivola Enrica, Russo Noemi Maria Carola, Tessitore Alessandro, Ciammola Andrea, Colosimo Carlo, de Rosa Anna, de Togni Laura, di Fonzo Alessio, Moschella Vincenzo, Pilotto Andrea, Spagnolo Francesca, Zangaglia Roberta, Barone Paolo, Picillo Marina, PSP‐NET study group

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Аннотация

BACKGROUND AND

OBJECTIVES

Caregivers of progressive supranuclear palsy (PSP) patients frequently show significant distress. The Parkinsonism Carers quality of life (QoL) (PQoL Carer) is a valid tool evaluating the effect of PSP on caregivers' QoL. Main aim of the present study was to develop a short version of the PQoL Carer, named PSP-ShoQoL Carer.

METHODS

PQoL Carer was administered within the PSP-NET. Participants underwent clinical, motor, cognitive, and behavioral evaluations.

RESULTS

Data from 344 participants were included. The final PSP-ShoQoL Carer included eight items. The internal consistency was high (Cronbach's α = 0.867) and PSP-ShoQoL Carer showed also good acceptability, reliability, and validity. The PSP-ShoQoL Carer showed a significant correlation with caregivers' standard measures of QoL and with patients' motor, cognitive, and behavioral characteristics, such as neuropsychiatric symptoms. Finally, PSP-ShoQoL Carer showed an appropriate sensitivity to change over 6-month follow up.

CONCLUSIONS

PSP-ShoQoL Carer is a reliable and valid time-saving tool for the assessment of caregivers' QoL in PSP.

Для цитирования: Cappiello Arianna, Calandra-Buonaura Giovanna, Ceravolo Roberto, Coralli Saverio, Cuoco Sofia, Del Prete Eleonora, di Biasio Francesca, Frosini Daniela, Gualtieri Vittorio, Mascioli Davide, Sambati Luisa, Schirinzi Tommaso, Stefani Alessandro, Umbertini Elisa, Aiello Marco, Costanzo Matteo, de Micco Rosa, Fabbrini Giovanni, Failla Gaetano, Longo Chiara, Malaguti Maria Chiara, Modugno Nicola, Olivola Enrica, Russo Noemi Maria Carola, Tessitore Alessandro, Ciammola Andrea, Colosimo Carlo, de Rosa Anna, de Togni Laura, di Fonzo Alessio, Moschella Vincenzo, Pilotto Andrea, Spagnolo Francesca, Zangaglia Roberta, Barone Paolo, Picillo Marina, PSP‐NET study group. A Short Version of Carers' Quality of Life Questionnaire for Parkinsonism: Data from Progressive Supranuclear Palsy Network.. Movement disorders clinical practice. 2025. DOI: 10.1002/mdc3.70389.

Предметные рубрики MeSH

Humans Quality of Life Caregivers Male Female Supranuclear Palsy, Progressive Aged Surveys and Questionnaires Middle Aged Reproducibility of Results Parkinsonian Disorders Aged, 80 and over

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