- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05755542
Long-Covid in Patients Post Rehabilitation Treatment and Reintegration Into Everyday Life
Occurrence of Long-Covid in Patients After Inpatient Rehabilitation Due to Acute Covid-19 Infection. How Easy is it for Patients to Return to Everyday Life and Work After Inpatient Rehabilitation Due to Acute Covid-19-infection?
The aim of the first study is to investigate how often a long Covid syndrome occurs after an inpatient rehabilitation due to previous hospitalization because of after acute Covid and whether there might be a connection with the severity during acute illness. 3 clusters of acute cases have been identified to be studied with regard to the long-term symptoms
- Mild course (medication, oxygen)
- Moderate course (IPS-IMC with NIV but without intubation)
- Severe course (intubation)
The aim of the second study is to use a catamnestic survey and subsequent evaluation of the information to gain an insight into the existing functional deficits relevant to everyday life and restriction of the ability to participate in the workplace after rehabilitation treatment. The assessment of functional deficits is carried out in relation to:
- Deficits in everyday skills (ADLs)
- Restrictions in the ability to participate in the profession.
Study Overview
Status
Conditions
Detailed Description
All patients who had been infected with Walenstadtberg after acute Covid infection were included.
Patients were hospitalized for inpatient rehabilitation in the period from 01.04.2020 to 30.06.2022.
A written follow-up survey was carried out with regard to a possible persistent long Covid symptoms and possible persistent deficits in everyday skills and Restrictions in the ability to participate in the profession. There are 2 cohort studies.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Jaroslaw A Dudczak, MD
- Phone Number: 0041793414160
- Email: jaroslaw.dudczak@kliniken-valens.ch
Study Contact Backup
- Name: Claudia von Felten, MD
- Email: clavofe21@hotmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- >18 years of age
- treated at a rehabilitation facility after being hospitilized for covid-19 infection
- complete questionnaire
- written consent to use collected data
Exclusion Criteria:
- < 18 years
- incomplete questionnaire
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Occurance of Symptoms pointing at Long-Covid after rehabilitation treatment
Time Frame: 2 years
|
Occurance of Symptoms pointing at Long-Covid after rehabilitation treatment
|
2 years
|
Occurance of deficits in managing everyday life and work after covid infection
Time Frame: 2 years
|
Investigation of deficits experienced by patients who have been treated at a rehabilitation facility after beeing hospitilized for a covid-19 infection and the impact of these deficits in everday life as well as in the workplace
|
2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
reinfection with covid-19 after rehabilition treatment
Time Frame: 2 years
|
reinfection with covid-19 after rehabilition treatment
|
2 years
|
Impact of Covid-19 infection on quality of life
Time Frame: 2 years
|
Impact of Covid-19 infection on quality of life in patients who have been treated at a rehabilition facility after beeing hospitilized due to a covid-19 infection
|
2 years
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Stefan Bachman, Prof., Rehazentrum Walenstadtberg
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Covid Outcome
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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