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

Cappiello, A., Calandra‐buonaura, G., Ceravolo, R., Coralli, S., Cuoco, S., Del Prete, E., et al. (2026). A Short Version of Carers' Quality of Life Questionnaire for Parkinsonism: Data from Progressive Supranuclear Palsy Network. MOVEMENT DISORDERS CLINICAL PRACTICE, 13(4), 1038-1043 [10.1002/mdc3.70389].

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

Mascioli, Davide;Schirinzi, Tommaso;Stefani, Alessandro;Olivola, Enrica;
2026-04-01

Abstract

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
apr-2026
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore MEDS-12/A - Neurologia
English
motor symptoms
neuropsychiatric symptoms
progressive supranuclear palsy
Cappiello, A., Calandra‐buonaura, G., Ceravolo, R., Coralli, S., Cuoco, S., Del Prete, E., et al. (2026). A Short Version of Carers' Quality of Life Questionnaire for Parkinsonism: Data from Progressive Supranuclear Palsy Network. MOVEMENT DISORDERS CLINICAL PRACTICE, 13(4), 1038-1043 [10.1002/mdc3.70389].
Cappiello, A; Calandra‐buonaura, G; Ceravolo, R; Coralli, S; Cuoco, S; Del Prete, E; Di Biasio, F; Frosini, D; Gualtieri, V; Mascioli, D; Sambati, L; ...espandi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/459943
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