COVID 19 and Psychological Health: a Cross Sectional Study to Evaluate Anxiety and Depression in Covid-19 Patients

NCT ID: NCT04689464

Last Updated: 2021-06-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

450 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-12-01

Study Completion Date

2021-06-01

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The covid-19 pandemic started to spread worldwide since December 2019. It promoted to an exaggerated psychological stress and anxiety in humans due to the intolerable symptoms higher than usual death of many infected patients. This study examines the corona related anxiety and if there is need for drug intervention to treat this anxiety.

To answer these questions, a survey made to the hospitalized patients including sex, age, educational level, Marital state, and a standardized questionnaires (GAD-7 and PHQ-9) which has been validated and shown to possess good psychometric qualities in studies of participants from multiple populations.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Covid19 Anxiety Depression

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_ONLY

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

mild covid

No interventions assigned to this group

moderate covid

No interventions assigned to this group

severe covid

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

\- patients with COVID19 willing to participate in the study

Exclusion Criteria

* unwilling unable to read or interact with standardized questionnaire unconscious
Minimum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

University of Basrah

OTHER

Sponsor Role collaborator

Ministry of Health, Iraq

NETWORK

Sponsor Role collaborator

Alhasan Mujtaba Al-Mudhaffer

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Alhasan Mujtaba Al-Mudhaffer

Clinical Pharmacy Specialist

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Zainab N Abdul-nabi, M.Sc.

Role: STUDY_DIRECTOR

University of Basrah

Hiba Dawood, M.Sc.

Role: STUDY_DIRECTOR

University of Basrah

Qussay N Almaliki, Ph.D.

Role: STUDY_DIRECTOR

AlFayhaa teaching hospital

Nadheera F Neamah

Role: STUDY_DIRECTOR

University of Basrah

Dania Zydoon

Role: PRINCIPAL_INVESTIGATOR

Al-Sader teaching hospital

Zainab Mahdi

Role: PRINCIPAL_INVESTIGATOR

Al-Mawani general hospital

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

AlFayhaa Teaching hospital

Basra, , Iraq

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Iraq

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

1120

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.