The Psychological Impact of the COVID-19 on Students.

November 27, 2021 updated by: Dr. Agnes Yuen-Kwan Lai, The University of Hong Kong

Exploring the Psychological Impact of the COVID-19 on Higher Education Students

The COVID-19 outbreak has been rapidly transmitted in late January 2020 and aroused enormous attention globally. The public at large may also experience boredom, disappointment, and irritability under the isolation measures. Depression and anxiety are common mental health problems experienced by university students. This survey aims to investigate the psychological impact of COVID 19 on students.

Study Overview

Status

Recruiting

Detailed Description

The COVID-19 outbreak has been rapidly transmitted in late January 2020 and aroused enormous attention globally. Infected patients may develop severe and even fatal respiratory diseases (e.g., acute respiratory distress syndrome (ARDS) and acute respiratory failure) ending up in intensive care. Apart from physical suffering, it is not uncommon for confirmed or suspected cases of COVID-19 to suffer from great psychological pressure and other health-related problems. The limited knowledge of the COVID-19 and the overwhelming news may lead to anxiety and fear in the public. The public at large may also experience boredom, disappointment, and irritability under the isolation measures.

Depression and anxiety are common mental health problems experienced by university students. Being in higher education is associated with many stressors and transitional events, and students fall within the age range when common mental health problems are at their developmental peak. Depression and anxiety can impair students' academic performance and social functioning, cause significant burden at university, and potentially affect their future career opportunities. The study includes 2 parts. Part A is an online survey study with non-probabilistic convenience sampling and part B is focus group interviews.

This study aims to explore the psychological impact of COVID-19 and coping methods in higher education students.

Study Type

Observational

Enrollment (Anticipated)

300

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: LAI YK Agnes, PhD
  • Phone Number: +85239176779238
  • Email: agneslai@hku.hk

Study Contact Backup

  • Name: Kelvin MP Wang, PhD
  • Phone Number: +85239176636
  • Email: mpwang@hku.hk

Study Locations

      • Hong Kong, Hong Kong, 852
        • Recruiting
        • LAI Agnes
        • Contact:
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 100 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Part A: An online survey study with non-probabilistic convenience sampling n=384

Part B: Focus group interviews n=32

Description

Inclusion Criteria:

• Higher education students aged 18 years and above

Exclusion Criteria:

• Subjects refuse to answer this questionnaire

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Stress level
Time Frame: baseline
measured by Stress Scale
baseline

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Anxiety and depressive symptoms
Time Frame: baseline
measured by a 4-item Patient Health Questionnaire
baseline
Insomnia symptoms and the associated daytime impairment
Time Frame: baseline
measured by 7-item Insomnia Severity Index
baseline
Psychological response to trauma
Time Frame: baseline
measured by a 22-item Impact of Event Scale -Revised
baseline
Resilience
Time Frame: baseline
measured by a 2-item Connor-Davidson Resilience Scale
baseline
Attitude and practice students regarding preventive measures
Time Frame: baseline
measured by outcome-based questionnaire
baseline

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Agnes YK Lai, PhD, School of Nursing, The University of Hong Kong

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

April 28, 2020

Primary Completion (Anticipated)

December 31, 2022

Study Completion (Anticipated)

December 31, 2023

Study Registration Dates

First Submitted

April 25, 2020

First Submitted That Met QC Criteria

April 25, 2020

First Posted (Actual)

April 28, 2020

Study Record Updates

Last Update Posted (Actual)

December 10, 2021

Last Update Submitted That Met QC Criteria

November 27, 2021

Last Verified

November 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • UW20-298

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

It was not included in the participants' consent.

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

Clinical Trials on Mental Health Wellness 1

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