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CompletedNCT06295315PROPSICOPWSUpdated Apr 30, 2025

Evaluation of the Psychological Profile of Adult Patients With Prader-Willi Syndrome

An observational study in Prader-Willi Syndrome, sponsored by Istituto Auxologico Italiano. Completed at 1 site in Italy. Open to participants aged 18 Years to 55 Years. Per ClinicalTrials.gov, last updated 2025-04-30.

Sponsored by Istituto Auxologico Italiano · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
36
Ages
18 Years to 55 Years
Sex
All
01

Study summary

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.

Read the detailed 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:

  • anthropometric parameters (height, weight, BMI, waist circumference);
  • socio-demographic conditions (gender, age, origin, level of education, family composition)
  • concomitant hormonal and psychiatric therapies
  • intellectual profile through the Mini-Mental State Examination (MMSE), a neuropsychological test consisting of 30 items that refer to the following cognitive areas: orientation in time, orientation in space, word recording, attention and calculation, recall, language, constructional praxis.
  • psychological well-being through the Psychological General Well-Being Index (PGWBI), a questionnaire made up of 22 items that measure the following dimensions: anxiety, depression, positivity and well-being, self-control, general state of health, and vitality.
  • perception of life quality through the 36-Item Short Form Survey (SF-36), a questionnaire composed of 36 items that investigates the perception of quality of life in relation to: physical functioning, limitations due to physical health, limitations due to emotions, energy and fatigue, emotional well-being, social activities, pain, general health perception
  • mental distress through the Symptom Checklist-90-R (SCL-90-R), a questionnaire made up of 90 items capable of investigating the presence and severity of symptoms of mental distress related to nine psychopathological dimensions: somatization, obsession-compulsion, interpersonal sensitivity, depression, anxiety, anger-hostility, phobic anxiety, paranoid ideation, psychoticism.

The following variables will be investigated in the parents or caregivers of subjects with PWS:

  • psychological distress through the Depression, Anxiety, and Stress Scale (DASS-21), a questionnaire composed of 21 items aimed at investigating experiences of anxiety, depression, and stress
  • psychological well-being through the Psychological General Well-Being Index (PGWBI), a questionnaire made up of 22 items that measure the following dimensions: anxiety, depression, positivity and well-being, self-control, general state of health, and vitality.
  • coping strategies through Coping Orientation to Problem Experienced (COPE-new Italian version). It is a questionnaire made up of 60 items aimed at investigating how often the subject implements - in difficult or stressful situations - different coping strategies to deal with stressful daily situations.
  • hyperphagia of subjects with PWS through the Hyperphagia Questionnaire (HQ), a questionnaire to be administered to parents or caregivers of reference consisting of 11 items capable of investigating the hyperphagia of subjects affected by PWS.
02

Conditions studied

  • Prader-Willi Syndrome

Keywords

  • Prader-Willy syndrome
  • Psychological well-being
  • Quality of life
  • Psychological distress
03

In context

Prader-Willi Syndrome

138 studies on the registry are indexed under Prader-Willi Syndrome; 24 are open to participants now.

This study's enrollment of 36 is below the median of 52 across 34 observational studies indexed under Prader-Willi Syndrome.

Browse Prader-Willi Syndrome studies →

Lead sponsor

Istituto Auxologico Italiano is the lead sponsor of 196 studies on the registry; 78 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 55 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Subjects with a genetic diagnosis of PWS, hospitalized at the Division of Auxology, Istituto Auxologico Italiano, Piancavallo-Verbania (Italy) for a 3-week body weight reduction program

Eligibility 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)

05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
36 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. Psychological well-being through the Psychological General Well-Being Index (PGWBI)

    A neuropsychological test consisting of 30 items that refer to the following cognitive areas: orientation in time, orientation in space, word recording, attention and calculation, recall, language, constructional praxis.

    Time frame: Baseline

  2. Perception of life quality through the 36-Item Short Form Survey (SF-36)

    A questionnaire composed of 36 items that investigates the perception of quality of life in relation to: physical functioning, limitations due to physical health, limitations due to emotions, energy and fatigue, emotional well-being, social activities, pain, general health perception

    Time frame: Baseline

  3. Mental distress through the Symptom Checklist-90-R (SCL-90-R)

    A questionnaire made up of 90 items capable of investigating the presence and severity of symptoms of mental distress related to nine psychopathological dimensions: somatization, obsession-compulsion, interpersonal sensitivity, depression, anxiety, anger-hostility, phobic anxiety, paranoid ideation, psychoticism.

    Time frame: Baseline

Secondary outcomes

  1. Psychological distress through the Depression, Anxiety, and Stress Scale (DASS-21)

    A questionnaire composed of 21 items aimed at investigating experiences of anxiety, depression, and stress

    Time frame: Baseline (investigated in the parents or caregivers of subjects with PWS)

  2. Coping strategies through Coping Orientation to Problem Experienced (COPE-new Italian version).

    A questionnaire made up of 60 items aimed at investigating how often the subject implements - in difficult or stressful situations - different coping strategies to deal with stressful daily situations.

    Time frame: Baseline (investigated in the parents or caregivers of subjects with PWS)

  3. Hyperphagia of subjects with PWS through the Hyperphagia Questionnaire (HQ)

    A questionnaire to be administered to parents or caregivers of reference consisting of 11 items capable of investigating the hyperphagia of subjects affected by PWS.

    Time frame: Baseline (investigated in the parents or caregivers of subjects with PWS)

07

Study locations

1 site
  • Istituto Auxologico Italiano IRCCS, site Piancavallo
    Oggebbio, Verbania 28824, Italy
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 30, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06295315
Lead sponsor
Istituto Auxologico Italiano
Responsible party
Sponsor
First posted
Mar 6, 2024
Start date
Apr 21, 2023
Primary completion
May 31, 2024
Completion
May 31, 2024
Last update
Apr 30, 2025
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Apr 2025. You cannot join it, but the record below documents what was studied.

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