- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02837406
Evaluation of the Health Digital Territories Program in the Five Pilot Territories (EvaTSN Project ) (EvaTSN)
May 12, 2022 updated by: University Hospital, Bordeaux
Evaluation of the Implementation and Results of the Health Digital Territories Program in the Five Pilot Territories (EvaTSN Project )
The aim is to evaluate a national health information technology-based program to improve healthcare coordination and access to information.
Study Overview
Status
Completed
Detailed Description
Improvement of coordination of all health and social care actors in the patient pathways is an important issue in many countries; Health Information (HI) technology has been considered as a potentially effective answer to this issue.
The French Health Ministry first funded the development of five TSN ("Territoire de Soins Numérique" / Digital health territories) programs, aiming at improving healthcare coordination and access to information for healthcare providers, patients or the population, and at improving healthcare professionals work organization; The French Health Ministry then launched a call for grant to fund one Eva TSN project consisting in evaluating the TSN programs implementation and impact and to develop a model for HI technology evaluation.
Study Type
Observational
Enrollment (Actual)
150
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Chalon-sur-Saône, France, 71100
- Agences Régionales de Santé Bourgogne
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LYON cedex, France, 69418
- Agence régionale de santé de Rhône Alpes
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Mont de Marsan, France, 40100
- Agences Régionales de Santé Aquitaine
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Paris, France, 75019
- Agence Régionale de Santé (ARS) Ile-de-France
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Saint-Denis, France, 97743
- Agence Régionale Santé Océan Indien
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Health professionals, primary care physicians (General Practitioner ), other liberal medical professionals, hospital practitioners, field professionals, medical social, users of evaluated systems, patients, industrial responsable of digital health program
Description
- Patients(people living in the five pilot territories of the Health Digital Territories program and the five control territories
- 'Users' who used the devices implemented, including platforms computerized,
- "Health professionals" : which includes both the health professions, medical and social professionals and groups representing them (URPS, etc.) and health facilities
- "Governance bodies" such as Regional Hospitalization Agency, the local authorities, etc.
- Manufacturers responsable for implementation of considered digital solutions.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
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Doctors
specialists and general practitioners by ich territory
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Health professionals
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Medical-social institutes
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Type and number of services developed for professionals
Time Frame: June 2018
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June 2018
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Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
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Number of users who are familiar with the program
Time Frame: June 2018
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June 2018
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Number of users (professional and / or patient / citizen)
Time Frame: June 2018
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June 2018
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Number of clicks by professional and / or user patient / citizen
Time Frame: June 2018
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June 2018
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Online time (start, end) by professional and / or user patient / citizen
Time Frame: June 2018
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June 2018
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Relevance rate of short stay admissions
Time Frame: june 2018
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june 2018
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Rates of preventable hospital stays
Time Frame: June 2018
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June 2018
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Rate of irrelevant drug prescriptions
Time Frame: June 2018
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June 2018
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Rate of recourse to prevention programs
Time Frame: June 2018
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June 2018
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Louis-Rachid SALMI, MD, PhD, University Hospital, Bordeaux
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 20, 2015
Primary Completion (Actual)
October 30, 2019
Study Completion (Actual)
October 30, 2019
Study Registration Dates
First Submitted
July 15, 2016
First Submitted That Met QC Criteria
July 15, 2016
First Posted (Estimate)
July 19, 2016
Study Record Updates
Last Update Posted (Actual)
May 19, 2022
Last Update Submitted That Met QC Criteria
May 12, 2022
Last Verified
May 1, 2022
More Information
Terms related to this study
Other Study ID Numbers
- CHUBX2014/42
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
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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