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The primary aim of the present study is to investigate the psychological profile of adult patients with PWS and the fatigue experienced by family members. Specifically, the level of psychological well-being, the subjective perception of life quality, and the main characteristics present in terms of psychopathological functioning of subjects with PWS will be investigated. These variables will be investigated in order to detect their presence and the main bonds of interaction, either between them or with other socio-demographic data, in a sample of adults with PWS. At the same time, the presence of psychological distress, levels of well-being quality of life, and coping strategies in family members and caregivers of individuals with PWS will be investigated.
Full description
The observational study will be carried out at the U.O. of Auxology, Istituto Auxologico Italiano, IRCCS, Piancavallo.
36 subjects with a genetic diagnosis of PWS, of both sexes and aged between 18 and 55, and their caregivers will be taken into consideration.
In subjects affected by PWS, the following variables will be investigated:
The following variables will be investigated in the parents or caregivers of subjects with PWS:
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Inclusion and exclusion criteria
Inclusion Criteria: subjects with a genetic diagnosis of PWS capable of understanding the questionnaires
Exclusion Criteria: subjects with a genetic diagnosis of PWS with cognitive problems (evaluated throughout the Mini-Mental State Examination)
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Central trial contact
Alessandro Sartorio, MD; Luca Grappiolo, Dr.
Data sourced from clinicaltrials.gov
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