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Clinical Trials/NCT05062590
NCT05062590
Recruiting
N/A

Socio-geriatric Evaluation (ESOGER): A Clinical Tool in Telehealth to Fight Against Vulnerable Seniors's Health Alterations and Social Isolation

Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal1 site in 1 country260 target enrollmentApril 4, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Social Isolation
Sponsor
Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal
Enrollment
260
Locations
1
Primary Endpoint
Autonomy
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

With the COVID-19 pandemic, elderly people (EP) living at home have seen their health deteriorated, thus increasing their needs in support and care. Indeed, while it was estimated that before the pandemic120 000 unattended living at home EP required care and services (taking bath, access to medication and food, etc.), the number doubled after COVID-19. Therefore, the waiting list for socio-medical services for unattended vulnerable clientele without a family doctor grew from 1300 à 1715 EP in a couple of months during the pandemic. With these numbers, it becomes clear that an intervention is needed. Truly, the Institut National d'Excellence en Santé et Services Sociaux (INESSS) conclude that it was pivotal to first identify the most vulnerable EP and second re-orient them according to their needs. Thus the investigator developed the Évaluation et orientation SOcio-GÉRiatrique (ESOGER) questionnaire available on a secure digital plateform enabling both a rapid evaluation and intervention to asses EP needs and provide the adequate ressources. Investigator's previous research has demonstrated that ESOGER is one of the rare clinical tools of first contact in telehealth while being global, multidimensional, and equitable. For this study, the investigator aims to evaluate the effect of ESOGER on EP physical and mental health, loss of autonomy, social isolation, quality of life and ressources consumption.

Registry
clinicaltrials.gov
Start Date
April 4, 2022
End Date
March 2026
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal
Responsible Party
Principal Investigator
Principal Investigator

Olivier Beauchet

MD, PhD, Senior researcher, Director of laboratory

Centre integre universitaire de sante et de services sociaux du Centre-Sud-de-l'Île-de-Montréal

Eligibility Criteria

Inclusion Criteria

  • Aged 65 and more
  • Living at home on the territory CIUSSS-Centre-Sud de l'île-de-Montréal (CCSMTL) of Jeanne-Mance
  • Brief Geriatric Assessment (BGA) score of 1/14 or more defining a severly to milidly frail health.

Exclusion Criteria

  • Principal address outside of the CCSMTL's Jeanne-Mance territory
  • Participate at another clinical trial, to avoid interferences
  • Not understand written or spoken French or English, questionnaires are only available in French and English.

Outcomes

Primary Outcomes

Autonomy

Time Frame: 3 months

ADL scale score from 0= very dependent to 6= very independent and IADL scale score 0= not autonomous 4= autonomous.

Social health

Time Frame: 3 months

Issues related to medication and food delivery and access to home care. Presence or not of a shortage in food, medication and home care ( binary question)

Socio-economic characteristics

Time Frame: 3 months

Presence or not of socio-economic problems (binary questions)

Participant's Quality of life

Time Frame: 3 months

Measured by the EQ-5D scale with two parts, scale 1 score from 1= no problem to 5 ( sever health problems) and scale 2 visual analogic scale score from 0= worst possible health to 100= best possible health.

COVID-19 symptoms

Time Frame: 3 months

presence or not of fever, cough, and shortness of breath (binary question)

psychological fraility

Time Frame: 3 months

Anxiety verbal analogic scale, score from 0= no anxiety to 10= extremly anxious

Secondary Outcomes

  • Caregiver burden(3 months)

Study Sites (1)

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