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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04365348
Other study ID # UW20-300
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date May 27, 2020
Est. completion date June 30, 2023

Study information

Verified date November 2021
Source The University of Hong Kong
Contact Agnes YK Lai, PhD
Phone 39176328
Email agneslai@hku.hk
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Patients with COVID-19 diagnoses are treated under isolation in hospitals and with high-stress level. Currently, there is little information on the mental health implications of exposure amongst COVID-19 survivors and their family members. Research exploring the psychological impact amongst survivors of exposure to COVID-19 is desperately needed to understand the effects, mental health toll, and support required in survivors of COVID-19. This study aims to assess the psychological impact of the COVID-19 outbreak on COVID-19 survivors and their family members.


Description:

Since the 2019 coronavirus disease (COVID-19) was first reported, it has been rapidly transmitted and has aroused enormous global attention. Infected patients may develop severe and even fatal respiratory symptoms such as acute respiratory distress syndrome (ARDS) and acute respiratory failure, ending up in intensive care. Patients with COVID-19 diagnoses are treated under isolation in hospitals and with high-stress level. The stress and psychological impact on patients were also correlated significantly with several adverse psychological effects, such as fatigue, fear of social contact, poor sleep, loneliness, and depressed mood. The psychological impact of COVID-19 may also evolve and last for a prolonged period after discharge from the hospital. However, there is currently little information on the mental health implications of exposure amongst COVID-19 survivors and their family members. Research exploring the psychological impact amongst survivors of exposure to COVID-19 is desperately needed to understand the effects, mental health toll, and support required in survivors of COVID-19. This study aims to assess the psychological impact of the COVID-19 outbreak on COVID-19 survivors and their family members.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date June 30, 2023
Est. primary completion date May 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - COVID-19 survivors (i.e., diagnosed with COVID-19 and discharged from the hospital) and/or a family member of a COVID-19 survivor; - Aged 18 years or above; - No medical diagnosis of psychiatric illness Exclusion Criteria: • Refusal to give consent

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Hong Kong Agnes Hong Kong

Sponsors (2)

Lead Sponsor Collaborator
The University of Hong Kong Queen Mary Hospital, Hong Kong

Country where clinical trial is conducted

Hong Kong, 

References & Publications (2)

Chua SE, Cheung V, McAlonan GM, Cheung C, Wong JW, Cheung EP, Chan MT, Wong TK, Choy KM, Chu CM, Lee PW, Tsang KW. Stress and psychological impact on SARS patients during the outbreak. Can J Psychiatry. 2004 Jun;49(6):385-90. — View Citation

Wang D, Hu B, Hu C, Zhu F, Liu X, Zhang J, Wang B, Xiang H, Cheng Z, Xiong Y, Zhao Y, Li Y, Wang X, Peng Z. Clinical Characteristics of 138 Hospitalized Patients With 2019 Novel Coronavirus-Infected Pneumonia in Wuhan, China. JAMA. 2020 Mar 17;323(11):1061-1069. doi: 10.1001/jama.2020.1585. Erratum in: JAMA. 2021 Mar 16;325(11):1113. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Stress level measured by the 10-item Perceived Stress Scale 1 month
Secondary Stress level measured by the 10-item Perceived Stress Scale 3 months
Secondary Negative emotion measured by the 13-item Hospital Anxiety and Depression Scale 3 months
Secondary Psychological response to trauma measured by the 22-item Impact of Event Scale -Revised 1 month and 3 months
Secondary Severity of insomnia symptoms and the associated daytime impairment measured by the 7-item Insomnia Severity Index 1 month and 3 months
Secondary Resilience measured by the 2-item Connor-Davidson Resilience Scale 1 month and 3 months
Secondary Quality of family functioning measured by 3-item Family Functioning Subscale 1 month and 3 months
Secondary Social support measured by 6-item social support questionnaire 1 month and 3 months
Secondary Psychological effects measured by 10-item outcome-based questionnaire 1 month and 3 months
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