- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05435469
The Changes of Coping With Stressful Events Among Adolescents Under the COVID-19 Pandemic.
May 22, 2023 updated by: Wei XIA, PhD
Study on the Changes of Coping Strategies With Stressful Events and Mental Health Level Among Adolescents Before and After COVID-19 Pandemic.
This study aims to describe the changes in coping strategies used by adolescents for stressful life events under the background of epidemic normalization; and explore the causes of coping strategy changes of stressful life events under the background of normalization of the epidemic situation among adolescents.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Under the special background of normalization of the epidemic situation, this paper describes and discusses the subjective feelings, changes in coping strategies, and causes of adolescent stressful life events, and puts forward a coping mechanism model of stressful adolescent events, which reflects the psychological changes of adolescent groups in the era of the epidemic situation and provides the basis for subsequent intervention measures.
Study Type
Observational
Enrollment (Actual)
4300
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Guangdong
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Guangzhou, Guangdong, China, 510080
- XIAW
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-
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
14 years to 25 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Non-Probability Sample
Study Population
General adolescents
Description
Inclusion Criteria:
- Aged 14-25
- Chinese nationality, who has lived in China since the outbreak of the COVID-19 epidemic, and has experienced or is experiencing the epidemic and its normalization.
- Have the normal cognitive ability, expression ability, and social participation ability.
Exclusion Criteria:
- Be diagnosed with psychological or mental illness.
- Incapacitated or unable to provide informed consent.
- Patients with severe diseases.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Questionnaires assessed adolescents
① Teenagers aged 14-25.
② Chinese nationality, who has lived in China since the outbreak of the COVID-19 epidemic, and has experienced or is experiencing the epidemic and its normalization.
③ Have the normal cognitive ability, expression ability, and social participation ability.
|
Participants will be asked to respond to the demographic information sheet, Adolescent Self-Rating Life Events Check List, Coping Inventory For Stressful Situations, Social Skills Rating System, brief-symptom-inventory, and Wong and Law EI Scale.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Coping strategies used after the pandemic
Time Frame: Baseline
|
The Coping strategies used by the adolescents for the stressful life events after the COVID-19 pandemic will be measured by Coping Inventory For Stressful Situations with the 21-items.
|
Baseline
|
|
Coping strategies used before the pandemic
Time Frame: Baseline
|
The Coping strategies used by the adolescents for the stressful life events before the COVID-19 pandemic will be measured by Coping Inventory For Stressful Situations with the 21-items.
|
Baseline
|
|
Mental health
Time Frame: Baseline
|
The mental health level of the adolescents will be measured by brief-symptom-inventory with 53-items.
|
Baseline
|
|
Emotional Intelligence status
Time Frame: Baseline
|
The Emotional Intelligence status of the adolescents will be measured by Wong and Law EI Scale with 16-items.
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Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Stressful Life Events after pandemic
Time Frame: Baseline
|
The Stressful Life Events experienced by the adolescents after the COVID-19 pandemic will be measured by Adolescent Self-Rating Life Events Check List with the 27-items.
|
Baseline
|
|
Stressful Life Events before pandemic
Time Frame: Baseline
|
The Stressful Life Events experienced by the adolescents before the COVID-19 pandemic will be measured by Adolescent Self-Rating Life Events Check List with the 27-items.
|
Baseline
|
|
Social support
Time Frame: Baseline
|
The social support that the adolescent could approach will be measured by Social Skills Rating System with the 10-items.
|
Baseline
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Wei Xia, PhD, Sun Yat-sen University
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)
July 1, 2022
Primary Completion (Actual)
August 30, 2022
Study Completion (Actual)
December 31, 2022
Study Registration Dates
First Submitted
June 25, 2022
First Submitted That Met QC Criteria
June 25, 2022
First Posted (Actual)
June 28, 2022
Study Record Updates
Last Update Posted (Actual)
May 23, 2023
Last Update Submitted That Met QC Criteria
May 22, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- L2022SYSU-HL-044
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Plan Description
The non-identified IPD will be shared after the outcomes have been published.
IPD Sharing Time Frame
After the publication of the study
IPD Sharing Access Criteria
Researchers should contact the PI for approval of the study protocol.
IPD Sharing Supporting Information Type
- SAP
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.
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