Development of General Practitioners Screening Tool of Frail Older Old Community
NCT ID: NCT02087982
Last Updated: 2016-12-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
840 participants
OBSERVATIONAL
2014-01-31
2016-12-31
Brief Summary
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It has been shown that the integration of CGA in the decision-making and care management at hospital improves inpatient's health and functional status, and reduces mortality rate and healthcare expenditures. The effects of CGA in daily practice of general practitioners remain unknown.
Implementation of a systematic CGA for every older old community-dwellers performed by a general practitioner remains yet difficult because of number of issues. First, although the number of older old community-dwellers keeps increasing, the number of health care professional with geriatric skills does not. Second, CGA is a complex and time-consuming process. Third, CGA requires a multidisciplinary geriatric team that cannot support alone the care of all frail older old community-dwellers due to their limited number. An implication of non-geriatricians in CGA is therefore required.
Recently, it was confirmed that CGA cannot be applied to all older adults, and that the best compromise could be the use of a two-step approach. The first step is the identification by non-geriatricians of elderly inpatients at high risk of adverse outcomes using a screening tool, and the second step is a CGA by geriatricians with a diagnosis purpose.
None of existing tools used for screening is adapted to the population of elderly people who visit general practitioners.Thus, healthcare professionals working in ED need a simple, standardized and brief geriatric assessment (BGA) to identify as soon as possible frail older old community-dwellers requiring specialized geriatric care.
The investigators hypothesized that a BGA older old community-dwellers carried out by a general practitioner could predict the adverse health events (i.e. hospitalization, institutionalisation, medical consultations and death) occurring during a 6-months follow-up period before the evaluation.
Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Seniors
The study will be based on a 6-months assessment period, with two consecutive monitoring visits on enrollment.
Patient follow-up after 3 months will be conducted by telephone and monitoring after 6 months will be carried out as part of a routine consultation.
Each subject will have a BGA (Brief Geriatric assesment).
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* the patient comes to a normal medical consultation without any acute health problem,
* the patient lives at home,
* the patient is able to respond to questions he is asked,
* the patient has given his agreement to answer questions during the initial consultation, to answer further questions by telephone after 3 months and to return in 6 months for a further consultation,
* the life expectancy of the patient as estimated by the primary care practitioner is greater than 6 months.
* the patient has french nationality and is a member of a national Social Security scheme.
* if a close relation of the patient does not agree the patient to be part of the study.
Exclusion Criteria
80 Years
ALL
Yes
Sponsors
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University Hospital, Angers
OTHER_GOV
Gerontopôle des Pays de la Loire
OTHER
Responsible Party
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Principal Investigators
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Gilles Berrut, PhD
Role: PRINCIPAL_INVESTIGATOR
Nantes University Hospital
Locations
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Nord Pas de Calais
Leers, , France
Countries
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Other Identifiers
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Reperage - 23
Identifier Type: -
Identifier Source: org_study_id