The psychological well-being and health-related quality of life of patients admitted to the hospital with COVID-19.
Completed
- Conditions
- COVID-19
- Registration Number
- NL-OMON23092
- Lead Sponsor
- Franciscus Gasthuis & Vlietland Group
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 250
Inclusion Criteria
Above 18 years of age
- Admitted with symptoms suitable with COVID-19 (respiratory (dyspnea, coughing, sore throat, rhinorhea, saturation <94%, respiratory rate >24/minute) or gastro-intestinal (diarrhea, vomiting) for a duration >24 hours) and eventually tested for SARS-CoV-2 using PCR.
- Able to understand the Dutch language
Exclusion Criteria
- Patients who participate in interventional trials of which the outcomes interfere with the outcomes in the current study
- Patients without a formal home adress and without an e-mail address.
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The occurrence and severity of psychological distress, defined as either one or a combination of PTSD, depression and/or anxiety, at 1, 3 and 12 months after hospital discharge in patients admitted with symptoms suitable with COVID-19 during the COVID-19 pandemic.
- Secondary Outcome Measures
Name Time Method The health-related quality of life (HRQoL) at 1, 3 and 12 months after hospital discharge in patients admitted with symptoms suitable with COVID-19 during the COVID-19 pandemic.