- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05311241
Teleconsultation in Ambulatory Care in France (TELET)
Observational Study of the Use of the Service Giving Access to Teleconsultation in France by Telemedicine Companies
Teleconsultation is a telemedicine medical act carried out remotely via information and communication technologies. This medical procedure has been legal in France since 2010 and reimbursed by the National Health Insurance under certain conditions since 2018. In 2020, following the COVID-19 epidemic, the lockdowns and the extension of the scope of financial coverage, 17 million teleconsultations have been reimbursed.
To date, few scientific studies have been published in France to precisely describe the use of the service giving access to outpatient teleconsultation, in particular since the major increase in activity linked to the COVID-19 epidemic.
The objective is to describe the use of the service giving access to outpatient teleconsultation carried out in France by teleconsultation companies and compare the use of the teleconsultation service according to the medical density of the territory.
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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-
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Paris, France
- Les Entreprises de Télémédecine
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Patient who used the teleconsultation access service with one of the telemedicine companies member of the LET participating in the study
- Patient residing in France according to the written information (address and or postal code) given at registration to the telemedicine company
- Teleconsultation service used between August 1, 2021 and November 30, 2021
- Teleconsultation service used in the context of outpatient care (hospitals excluded)
- Teleconsultation service used for a teleconsultation with a doctor registered with the Medical Doctors Council in France
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Rate of patients without a treating doctor
Time Frame: Through the study completion at the time of the teleconsultation, average 1 day
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Through the study completion at the time of the teleconsultation, average 1 day
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Julie Salomon, MD, Qare
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
Other Study ID Numbers
- 001 (Buy Pharma Ecza Deposu San. Tic. Ltd.)
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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