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Effects of COVID-19 Forced Isolation Context on Adolescents With and Without Somatic Symptom Disorder

Somatic Symptom Disorder Clinical Trial

Official title:
Effects of a Pandemic Forced Isolation Context on Adolescents With Somatic Symptom Disorder. A Panel Study

Clinical Trial Summary

The purpose of this study is to evaluate whether a forced isolation context (such provided by the ongoing Covid-19 pandemic restrictive measures) could reduce the burden of somatic symptoms among a group of patients with Somatic Symptom Disorder (SSD). Secondary objective is to assess if a reduction in terms of depression tendency and anxiety occurs in this specific population and which are the effect of such a context among a group of adolescents without SSD. We want to compare these results with data obtained at the end of the pandemic.

Clinical Trial Description

This study aims to evaluate whether the forced isolation context provided by the ongoing Covid-19 pandemic is providing an advantage in terms of reduction of somatic symptoms burden among an Italian group of adolescents with SSD, assessed by the Patient Health Questionnaire (PhQ15) administered during and at the end of the pandemic. Secondary objectives of the study are: - To investigate the difference in anxiety and depression scores assessed by the Multidimensional Anxiety Scale for Children (MASC2) and Child Development Inventory (CDI-2) questionnaires among a group of SSD adolescents, during and after the pandemic isolation context. - To investigate the difference in anxiety and depression scores assessed by the Multidimensional Anxiety Scale for Children (MASC2) and Child Development Inventory (CDI-2) questionnaires among a group of adolescents without SSD, during and after the pandemic isolation context. - To compare the difference in anxiety and depression scores time modification between the two groups of adolescents. - To explore through tailored questions which adolescents' coping strategies are during a pandemic isolation context among SSD patients and a group of controls without SSD. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05795803
Study type Observational
Source IRCCS Burlo Garofolo
Contact
Status Completed
Phase
Start date April 1, 2020
Completion date May 31, 2020
View Details
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