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CompletedNCT04008472GERONTACCESSUpdated Jun 9, 2026

Telemedicine - Evaluation of the Impact of a Telemedicine Device (DTM) on the Prevention of Emergency Department Visits and Hospitalizations of Nursing Home Residents Aged Polypathological

An interventional study of Telemedecine in Polypathology, sponsored by University Hospital, Limoges. Completed at 1 site in France. Open to participants aged 60 Years and older. Per ClinicalTrials.gov, last updated 2026-06-09.

Sponsored by University Hospital, Limoges · Not applicable, Interventional, and Prevention

From the registry’s dates

  • Registered 3 years 8 months after the study started (first participant enrolled Nov 2015, registered Jul 2019).
Phase
Not applicable
Study type
Interventional
Enrollment
428
Allocation
Randomized
Ages
60 Years and older
Sex
All
01

Study summary

For several decades, there is an aging population, particularly in industrialized countries. This lengthening of the duration of life is accompanied by an increase in the number of chronically ill patients. On an estimate of 15 million patients in France today, the figure reported for 2020 would be 20 million patients. Chronic diseases are responsible for functional decompensation and admission responsible autonomy breaks in nursing homes (Accommodation Establishment of People Dependent Elderly).

An estimated 700,000 the number of people currently living in retirement homes in France. These residents are mostly dependent and multiple pathologies requiring regular general and specialist medical monitoring . Medical concern demographic outlook and the need for access to quality care across the country leads to the development of telemedicine.

The need for telemedicine is not the same throughout the territory. It is less, or different, in highly urbanized areas where the density of health professionals is high, then it can be a new response to the needs of rural, isolated or landlocked. Telemedicine promotes the development of the concept of graduated care sector, especially in the management of patients with chronic diseases.

Telemedicine in rural nursing homes and can be a tool for assessing, monitoring and coordination to avoid decompensation of chronic conditions and rehospitalization.

This organization can afford to break the isolation of general practitioners and EHPAD coordinators physicians in rural areas and provide access to several specialties.

02

Conditions studied

  • Polypathology

Keywords

  • Telemedecine
03

In context

Lead sponsor

University Hospital, Limoges is the lead sponsor of 255 studies on the registry; 36 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Resident in one of 9 nursing homes participating in the project
  • Resident polypathologique has at least two comorbidities
  • Having made no request to change place of residence at the time of the inclusion visit
  • Having given free consent, informed writing and signed by himself and / or his legal representative

Exclusion criteria

Exclusion Criteria:

  • Unaffiliated resident or non-receiving of social security
  • severe pathology (ies) involving life-threatening in the short term
  • Resident whose return home, transfer to another nursing home or to a long term care unit is programmed
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
428 participants (actual)

Study arms

  • Experimental
    Telemedecine

    Patients benefiting from telemedicine

    Other: Telemedecine

  • No intervention
    Control

    routine care without telemedecine

Interventions

  • OtherTelemedecine

    Initiation of tele-medical consultation with the resident, a caregiver for the nursing home, the referring physician and geriatrician téléexpert. After a overall geriatric assessment in nursing homes by UPSAV the first teleconsultation is organized within 10 days. Subsequent visits are scheduled every 3 months for 12 months. Spontaneous visits can be requested at the initiative of the referring physician.

06

What researchers measure

Primary outcomes

  1. Evaluation of telemedicine on prevention in old and polypathological patients

    Proportion of patients with emergency admission or unscheduled hospitalization in medical or surgical service over 12 months.

    Time frame: After 12 months

Secondary outcomes

  1. Medico-economic impact

    cost effectiveness of the telemedicine device

    Time frame: After 12 months

  2. Impact on recurring hospitalizations

    Number of readmissions

    Time frame: After 12 months

  3. Impact on overall health

    Number of emergency admissions Number of readmissions Number of days of hospitalization Number of medical consultations o

    Time frame: After 12 months

  4. Impact on the quality of life ( EQ5D questionnary)

    The EQ-5D (Europen Qyuality of llive) five dimension scale) questionnaire has two components: health state description and evaluation. In the description part, health status is measured in terms of five dimensions (5D); mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Mobility dimension asks about the person's walking ability. Self-care dimension asks about the ability to wash or dress by oneself, and usual activities dimension measures performance in "work, study, housework, family or leisure activities". In pain/discomfort dimension, it asks how much pain or discomfort they have, and in anxiety/depression dimension, it asks how anxious or depressed they are. Higher values represent a worse outcome. The scale ranges from 5 to 15.

    Time frame: After 12 months

  5. Impact on mortality

    Proportion of patients who died at 12 months

    Time frame: After 12 months

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Study locations

1 site
  • CHU de Limoges
    Limoges, 87042, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT04008472
Lead sponsor
University Hospital, Limoges
Responsible party
Sponsor
First posted
Jul 5, 2019
Start date
Nov 2015
Primary completion
Jan 2018
Completion
May 2019
Last update
Jun 9, 2026

Study contacts

Achille TCHALLA, Professor
principal investigator · University Hospital, Limoges

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jul 2019. You cannot join it, but the record below documents what was studied.

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