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Clinical Trials in France / NCT07792187
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Interest of Telemedicine in Primary Care in an Multidisability Population Institutionalized

NCT07792187 · tracked via the Priya Life Science France tracker
Phase
Not applicable
Started
2027-01
Last updated
2026-08-28

Condition(s) studied

Deglutition Disorders in Disabled Persons

Investigational drug(s) / intervention(s)

Experimental procedure: swallowing assessment by telemedicineStandard procedure: day hospitalization

Experimental procedure: swallowing assessment by telemedicine: The teleconsultation will be scheduled by the UVD programming IDE after contact by the structure team. This teleconsultation will take place in the presence of the patient's care assistant as well as medical staff (IDE, occupational therapist, physiotherapist, speech therapist, etc.) from the institution and a doctor specializing in swallowing and a speech therapist for the university hospital. The resident will do a food test under the eyes of CHU specialists. The patient will be able to test several textures (more or less solid/liquid) prepared in the center in order to be more accurate in their daily life. The meal will be in his familiar environment with his usual caregivers and tools. The CHU team will be able to interact directly with the institution's staff in order to have all the information necessary to determine their conclusions : questions, details on the patient's degree of compliance, etc.

Standard procedure: day hospitalization: Treatment for swallowing disorders in the hospital sector consists of the patient coming to the university hospital or to a day hospital in order to carry out a swallowing assessment consisting of invasive examinations such as nasofibroscopy (NF), swallowing fluoroscopy (VFS) as well as eating a meal outside the patient's usual context, sometimes in the presence of other people foreign to the patient (source of distractibility and sometimes anxiety).

Study summary

Swallowing disorders are common and fall within the scope of primary care (as basic, essential health services accessible to all individuals within a community). These swallowing disorders, strongly linked to the environment, do not require, in the majority of cases, a technical and intrusive evaluation. The main objective of this project is to study the relevance of an assessment of dysphagia by teleconsultation

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients aged ≥ 18 years living in a medical institution (MAS type, FAM from the ASEI network) * Indication of a medical swallowing assessment in hospital * Person affiliated to or beneficiary of a social security system. * Free, informed and written consent signed by the participant or their guardian Exclusion Criteria: * Participation in another research including a period of exclusion still ongoing * non-movable patient * Pregnant woman, Woman of childbearing age without contraception * any contraindication to nasofibroscopy and/or fluoroscopy

Primary outcome measure(s)

Trial sites (5)

FacilityCityRegionStatus
FAM la Vitarelle Montauban France
MAS de Granès Montauban France
Mas Azure Rieux-Volvestre France
Larrey Hospital - Toulouse University Hospital Toulouse France
MAS Jean de la Fontaine Toulouse France

More University Hospital, Toulouse trials in France

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07792187 on ClinicalTrials.gov ↗ ← All trials in France