- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04714138
Remote Video Consultation for Quality of Life Assessment in Patients Hospitalised After COVID-19 Infection (TELECOVID)
Remote Evaluation of Quality of Life and Functional Capacities in Patients Hospitalised for COVID-19: a Prospective Observational Study
Around 90.000 patients have been hospitalised due to COVID-19 infection in France between March 1st and June 15th; 19% of those requiring intensive care. Approximately 80% of these patients have been discharged home by September 30th. Nonetheless, COVID-19 infection along with intensive care consequences are very likely to impede those patients quality of life and functional capacities.
This study aims to describe the quality of life outcomes and functional capacities of COVID-19 survivors, at least 6 months after primary care hospital discharge.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Normandie
-
Montivilliers, Normandie, France, 76290
- Groupe Hospitalier Du Havre
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Adult patient
- COVID-19 hospitalisation at Le Havre hospital between March 1st and May 11th
- Non-opposition during first phone contact
Exclusion Criteria:
- Guardianship
- Juvenile patients
- Pregnancy
- Inability to communicate
- Cognitive disorders
- Deceased patient
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Health-related quality of life
Time Frame: 10 to 12 months after hospital discharge during remote video consultation
|
Measured with the Short-Form health survey (SF-36) scale (score ranging form 0 (worst score) to 100 (best score) per item)
|
10 to 12 months after hospital discharge during remote video consultation
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Functional capacity
Time Frame: 10 to 12 months after hospital discharge during remote video consultation
|
One-minute Sit-to-stand test
|
10 to 12 months after hospital discharge during remote video consultation
|
|
Independency
Time Frame: 10 to 12 months after hospital discharge during remote video consultation
|
KATZ score (ranging 0 (fully dependent) to 6 (fully independent))
|
10 to 12 months after hospital discharge during remote video consultation
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2020-A03110-39
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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