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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04357769
Other study ID # 152/20
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 10, 2020
Est. completion date April 25, 2020

Study information

Verified date February 2021
Source Federico II University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Despite being originated in Wuhan, in the China mainland region of the Hubei, Italy has been the hardest-hit country in the world by the COVID-19 pandemic during the month of March. Due to the uncontrollable spread of the contagion, the Italian Government has been forced to impose a series of restrictions and social distancing measures, culminating in the extension of lockdown to the entire Italian territory on March 8th. During this period, the general population has been overwhelmed by feelings of worry, anxiety, and discomfort. The discomfort is reinforced by the lengthening of the lockdown, to the point that it may be considered as a mass model of chronic or subchronic mild stress. The predictable effects of this stress on mental health have already been claimed, Post-traumatic symptoms were found in 7% among 285 Wuhan and surrounding cities' residents during the COVID-19 outbreak. A recent survey in the Italian general population reported similar outcomes. In this context, the psychic conditions of the most fragile ones, i.e. those already affected by a severe mental disorder, represent a major concern. Having a history of psychiatric illness is regarded as one of the most relevant predictors of a negative psychological impact of quarantine. Patients with severe mental disorders may be among the hardest hit subjects, as they may be more vulnerable by the COVID-19 outbreak for a series of clinical and psychological factors. In the Italian context, the vulnerability of these patients may be increased by the lockdown of mental health services as a consequence of mass quarantine and optimization of health resources toward action to contrast COVID-19-related sanitary emergencies. Despite several reports investigated the psychological effects of COVID-19 pandemic on health-care workers, COVID-19 affected people, or the general population, at the moment, no study has investigated the effects of the distress caused by fear of contagion and mass quarantine on severe mental disorder patients. The present study aimed at providing a first evaluation of anxiety, depressive, stress-related symptoms in these patients.


Recruitment information / eligibility

Status Completed
Enrollment 400
Est. completion date April 25, 2020
Est. primary completion date April 20, 2020
Accepts healthy volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - DSM-5 Diagnosis of Schizophrenia or Psychosis Spectrum; Bipolar Disorder; REcurrent Major Depressive Disorder - Linguistic and cognitive ability to complete the rating scales - Written informed consent - Psychopathological compensation at last clinical evaluation on January-February 2020 Exclusion Criteria: - SARS-CoV-2 positive, suspected positive, or in recent close contact with positive ones - Not under strict quarantine, due to work reasons or to any other reason allowing to overcome quarantine - Current or recent hospitalization (i.e. on March-April), for any reason - Intellectual disability - Psychiatric disturbances secondary to general medical conditions or substances - Serious medical conditions with infaust prognosis or severely affecting the quality of life - Living in Northern Italy Adjunctive Exclusion Criteria for the General Population and Caregivers: - Psychiatric Disorder, of any type Adjunctive Exclusion Criteria for the General Population: - First degree relative or caregiver of a psychiatric patient

Study Design


Intervention

Other:
PSS (Perceived Stress Scale)
Self-administered scale for the evaluation of the stress perceived by the subject in the last weeks
GAD-7 (7-item Generalized Anxiety Disorder)
Self-administered scale for the evaluation of anxiety symptoms in the last weeks
PHQ-9 (9-item Patient Health Questionnaire)
Self-administered scale for the evaluation of depressive symptoms in the last weeks
SPEQ (Specific Psychotic Experiences Questionnaire) - Paranoia and Grandiosity Subscales
Self-administered scale for the evaluation of sub-threshold psychotic symptoms in the last weeks
Zaritt Burden Interview
Self-administered scale for the evaluation of severe mental disorder patients' caregiver burden

Locations

Country Name City State
Italy University of Naples "Federico II" Napoli

Sponsors (1)

Lead Sponsor Collaborator
Federico II University

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perceived Stress Scale (PSS) outcome Significant differences among groups in the mean Perceived Stress Scale (PSS) score, which measures the stress severity perceived by the subjects in the last month. The scale is constituted by 10 items that are self-rated by the subject on a 0-4 Likert scale. The scale minimum total score is 0, the maximum is 40. Higher total scores indicate a worse outcome 10 days
Secondary Generalized Anxiety Disorder (GAD-7) scale outcome Significant differences among groups in the mean Generalized Anxiety Disorder (GAD-7) scale score, which measures anxiety symptoms' severity in the last two weeks. The scale is constituted by 7 items that are self-rated by the subject on a 0-3 Likert scale. The scale minimum total score is 0, the maximum is 21. Higher total scores indicate a worse outcome 10 days
Secondary Patient Health Questionnaire (PHQ-9) scale outcome Significant differences among groups in the mean Patient Health Questionnaire (PHQ-9) scale score, which measures depressive symptoms' severity in the last two weeks. The scale is constituted by 9 items that are self-rated by the subject on a 0-3 Likert scale. The scale minimum total score is 0, the maximum is 21. Higher total scores indicate a worse outcome 10 days
Secondary Specific Psychotic Experiences Questionnaire (SPEQ) - Paranoia subscale outcome Significant differences among groups in the mean Specific Psychotic Experiences Questionnaire (SPEQ) - Paranoia subscale score. The SPEQ scale is designed for the assessment of current sub-threshold psychotic symptoms in multiple domains. The Paranoia subscale measures persecutory/reference ideas and is constituted by 15 items that are self-rated by the subject on a 0-5 Likert scale. The subscale minimum total score is 0, the maximum is 75. Higher total scores indicate a worse outcome 10 days
Secondary Specific Psychotic Experiences Questionnaire (SPEQ) - Grandiosity subscale outcome Significant differences among groups in the mean Specific Psychotic Experiences Questionnaire (SPEQ) - Grandiosity subscale score. The Grandiosity subscale measures grandiosity/megalomaniac ideas and is constituted by 8 items that are self-rated by the subject on a 0-3 Likert scale. The subscale minimum total score is 0, the maximum is 24. Higher total scores indicate a worse outcome 10 days
Secondary Caregiver Burden Significant correlations between mean Zarit Burden Interview (ZBI) and mean scores on the Perceived Stress Scale (PSS). The ZBI is designed for the assessment of caregiver burden. The scale is constituted by 22 items that are self-rated by the subject on a 0-4 Likert scale. The scale minimum total score is 0, the maximum is 88. Higher total scores indicate a worse outcome 10 days
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