- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04357769
COVID-19 Pandemic Burden in Severe Mental Disease Patients (PsyCOVID)
A Study of Perceived Distress and Psychological Burden in Patients Suffering From Severe Mental Diseases During the COVID-19 Pandemic in Italy
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.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Napoli, Italy, 80131
- University of Naples "Federico II"
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
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 Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
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Patients
Individuals aged 18-70 years with a diagnosis of severe mental disorder (schizophrenia or psychosis spectrum disorder; bipolar disorder; major depressive disorder) who were in a condition of psychopathological compensation, had their last clinical evaluation at the University of Naples Federico II outpatient unit of Psychiatry during January-February 2020, were not positive or suspected positive for COVID-19, and were under strict quarantine
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Self-administered scale for the evaluation of the stress perceived by the subject in the last weeks
Self-administered scale for the evaluation of anxiety symptoms in the last weeks
Self-administered scale for the evaluation of depressive symptoms in the last weeks
Self-administered scale for the evaluation of sub-threshold psychotic symptoms in the last weeks
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Controls (General Population)
Individuals aged 18-70 years who had not a psychiatric condition nor were positive or suspected positive for COVID-19 and were under strict quarantine (e.g.
not getting out for work)
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Self-administered scale for the evaluation of the stress perceived by the subject in the last weeks
Self-administered scale for the evaluation of anxiety symptoms in the last weeks
Self-administered scale for the evaluation of depressive symptoms in the last weeks
Self-administered scale for the evaluation of sub-threshold psychotic symptoms in the last weeks
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First-degree Relatives
Individuals aged 18-70 years who were first-degree relatives and caregivers of an individual included in the Patients group, who had not a psychiatric condition nor were positive or suspected positive for COVID-19 and were under strict quarantine
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Self-administered scale for the evaluation of the stress perceived by the subject in the last weeks
Self-administered scale for the evaluation of anxiety symptoms in the last weeks
Self-administered scale for the evaluation of depressive symptoms in the last weeks
Self-administered scale for the evaluation of sub-threshold psychotic symptoms in the last weeks
Self-administered scale for the evaluation of severe mental disorder patients' caregiver burden
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Perceived Stress Scale (PSS) outcome
Time Frame: 10 days
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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
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10 days
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Generalized Anxiety Disorder (GAD-7) scale outcome
Time Frame: 10 days
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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
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10 days
|
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Patient Health Questionnaire (PHQ-9) scale outcome
Time Frame: 10 days
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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
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10 days
|
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Specific Psychotic Experiences Questionnaire (SPEQ) - Paranoia subscale outcome
Time Frame: 10 days
|
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
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10 days
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Specific Psychotic Experiences Questionnaire (SPEQ) - Grandiosity subscale outcome
Time Frame: 10 days
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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
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10 days
|
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Caregiver Burden
Time Frame: 10 days
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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
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10 days
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 152/20
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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