Validation Study of Oral Teleconsultation (EDENT2)

September 13, 2016 updated by: University Hospital, Montpellier

Validation Study of Oral Teleconsultation - Study EDENT2

In this study we want to evaluate the oral care pathway after an oral teleconsultation.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

An oral teleconsultation was proposed to the 461 residents of the public hospital of Uzès. A specifically trained nurse recorded 4 videos (1 per quadrant) per mouth with an intra-oral camera using fluorescent light (Soprocare®) and keyed in information about the resident (general state, identification,…). These data were recorded and sent onto a central secured server, through a specific piece of software (e-DENT®). The dentists from the University Hospital of Montpellier were then able to analyse the videos remotely, make a diagnosis and organise each resident's oral care.

Study Type

Observational

Enrollment (Actual)

700

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

14 years to 96 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

People who are in long-term care home with oral telemedicine activity

Description

Inclusion Criteria:

  • The subject is aged at least 18 years
  • Patients cared for in their host institution

Exclusion Criteria:

  • NA

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

  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Diagnostic of caries
Time Frame: 1 day
Teleconsultation will be made using a specific camera SoproCare®6, the company Acteon
1 day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Diagnostic of caries
Time Frame: 6 months
Teleconsultation will be made using a specific camera SoproCare®6, the company Acteon
6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University Hospital, Montpellier

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

March 1, 2014

Primary Completion (Actual)

September 1, 2016

Study Completion (Actual)

September 1, 2016

Study Registration Dates

First Submitted

September 7, 2016

First Submitted That Met QC Criteria

September 13, 2016

First Posted (Estimate)

September 16, 2016

Study Record Updates

Last Update Posted (Estimate)

September 16, 2016

Last Update Submitted That Met QC Criteria

September 13, 2016

Last Verified

February 1, 2014

More Information

Terms related to this study

Other Study ID Numbers

  • 9370

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

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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