COVID-19 Severity and Psychiatric Morbidity

Sponsor
Instituto Mexicano del Seguro Social (Other)
Overall Status
Recruiting
CT.gov ID
NCT05124158
Collaborator
Universidad Autonoma de Coahuila (Other)
50
1
8
6.3

Study Details

Study Description

Brief Summary

The COVID-19 pandemic represents the most serious global health threat since the Spanish influenza, with repercussions on physical and mental health. The balance between physical and mental state is essential when establishing treatment for a critically ill patient and must be taken into account by health professionals. Therefore, the investigators hypothesize that there is an association between the severity of the clinical picture of COVID-19 and psychiatric morbidity.

Objective. Associate the severity of the clinical picture of COVID-19 with psychiatric morbidity.

Material and method. Hospitalized participants in the COVID respiratory area at the General Hospital of the Zone will be included. # 51 of Gómez Palacio, Dgo. in the period from October 1, 2021 to March 31, 2022. This is an epidemiological, observational, prospective, longitudinal, analytical study. Sociodemographic, clinical and psychiatric evaluation data will be obtained using GMHAT / PC. A statistical analysis will be carried out using descriptive statistics (frequencies, measures of central tendency and dispersion) and analytical, to evaluate the association (Chi2) and to evaluate the effect of the intervening variables (binary logistic regression and multivariate regression). The data will be analyzed in the SPSS version 21 program.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Subjects who meet selection criteria entered into the COVID area will be included in the period from October 1, 2021 to March 31, 2022. A non-probabilistic convenience sampling will be carried out, occluding all patients who agree to participate and meet the criteria of selection.

    Patients entering the COVID area will be invited to participate in the study. Participants will be questioned about the selection criteria, and if they are eligible to be included in the study, they will be given the letter of informed consent for reading, clarification of doubts and signature. Each participant will receive a copy of the informed consent letter, this copy will remain in the COVID area until the participant is discharged. The researcher's copy will be handled under the biosafety standards established in the institute for materials and documents in contact with COVID patients.

    Information about their general data and conventional medical history will be obtained through direct questioning and review of the medical record and a brief neuropsychiatric evaluation will be performed. The severity data of the COVID clinical picture and clinical evolution will be obtained from the records in the electronic medical record. The evaluation of psychiatric morbidities using the GMHAT / PC will be carried out later, prior to feeding the database.

    The information obtained will be emptied into an Excel database for subsequent statistical analysis with the IBM SPSS STATISTICS program. The information of the study will remain confidential, the identity of the participants will be protected through the use of the initials of the participant's name. The data collected will be in charge of the researcher for safekeeping. The management of the information from the data collection sheets will be organized by folios.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    50 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Association of the Severity of the Clinical Picture of COVID-19 and Psychiatric Morbidity
    Actual Study Start Date :
    Oct 1, 2021
    Anticipated Primary Completion Date :
    Mar 31, 2022
    Anticipated Study Completion Date :
    May 31, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Patients with a diagnosis of COVID-19

    A directed psychiatric evaluation will be carried out and 1 evaluation instrument will be applied: Global Tool for the Evaluation of Mental Health in Primary Care (GMHAT / PC). The Global Mental Health Assessment Tool / Primary Care (GMHAT / PC) is a computerized, semi-structured clinical interview tool developed to assess and identify mental health problems. The main diagnosis derives from the use of a hierarchical model based on ICD-10. The diagnostic program takes into account the severity of symptoms (moderate to severe). It also generates alternative diagnoses and comorbidity states based on the presence of symptoms of other disorders. In addition, it includes a suicide risk assessment.

    Outcome Measures

    Primary Outcome Measures

    1. Degree of severity of the clinical picture of COVID-19 [Duration of hospitalization (20 days)]

      Severity of COVID-19 according to the clinical and paraclinical parameters established by the WHO (Mild, Moderate, Severe, Critical)

    2. Number of participants with depression [Duration of hospitalization (20 days)]

      According to the result of the psychiatric evaluation using GMHAT/PC: Absent or Present

    3. Number of participants with anxiety [Evaluation at hospital admission (2 hours)]

      According to the result of the psychiatric evaluation using GMHAT/PC: Absent or Present

    4. Number of participants with panic disorder [Evaluation at hospital admission (2 hours)]

      According to the result of the psychiatric evaluation using GMHAT/PC: Absent or Present

    5. Number of participants with psychosis [Evaluation at hospital admission (2 hours)]

      According to the result of the psychiatric evaluation using GMHAT/PC: Absent or Present

    Secondary Outcome Measures

    1. Clinical evolution of the participants measured by clinical and paraclinical parameters [Duration of hospitalization (20 days)]

      Worsening or improvement of the disease measurable by observable and diagnosable signs and symptoms according to the clinical and paraclinical parameters established by the WHO.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Beneficiaries in the COVID respiratory area of HGZ No.51

    • COVID-19 diagnosis confirmed by PCR.

    • Complete neuropsychiatric medical history data that allows the evaluation of the psychiatric status using GMHAT / PC

    • Accept to participate in the study and sign the informed consent.

    Exclusion Criteria:
    • Pre-existing neuropsychiatric diseases and under psychiatric medical treatment.

    • History of psychotropic use and / or withdrawal syndrome.

    • Incomplete file data or that do not allow the assessment of the severity of the clinical picture of COVID-19 upon admission to the respiratory area.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Instituto Méxicano del Seguro Social Gómez Palacio Durango Mexico 35025

    Sponsors and Collaborators

    • Instituto Mexicano del Seguro Social
    • Universidad Autonoma de Coahuila

    Investigators

    • Principal Investigator: Lilia E Luque Esparza, Dra., IMSS

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Lilia Edith Luque Esparza, Principal Investigator, Instituto Mexicano del Seguro Social
    ClinicalTrials.gov Identifier:
    NCT05124158
    Other Study ID Numbers:
    • R-2021-902-025
    First Posted:
    Nov 17, 2021
    Last Update Posted:
    Nov 17, 2021
    Last Verified:
    Nov 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Lilia Edith Luque Esparza, Principal Investigator, Instituto Mexicano del Seguro Social
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 17, 2021