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Clinical Trials/NCT02871557
NCT02871557
Completed
Not Applicable

Frail Elderly Subjects Martinique: Adverse Outcome After Hospitalisation in Geriatric Department

Société Martiniquaise de Gérontologie et Gériatrie0 sites287 target enrollmentJanuary 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Elderly People With Polypathology or Disabilities
Sponsor
Société Martiniquaise de Gérontologie et Gériatrie
Enrollment
287
Primary Endpoint
Mortality
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This was a prospective multicenter cohort study of elderly people admitted to the acute care for elders in Martinique. They were followed up to 36 months. It aimed to study the adverse outcomes. In all, 287 subjects were included. They were 85+/-6 years, and mainly women (61%).

Detailed Description

The SAFMA cohort was an ad hoc study formed into the recruitment of the acute care for elders in the geriatric department of Martinique university Hospitals. The inclusion of subjects ran from January 1st 2012 to June 30th 2012. To be eligible, patients had to be 75 or over and hospitalised for acute condition. Each patient was visited by a specialist in geriatrics familiar with the survey procedures. In the course of this interview, patients were informed about the study, prior to signing the consent form. If the clinical status and/or the cognitive status of the patient did not enable informed consent, the interviewer referred to the subject's representative. Follow-up was performed by visits and telephone interview till 36 months.

Registry
clinicaltrials.gov
Start Date
January 2012
End Date
June 2015
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Société Martiniquaise de Gérontologie et Gériatrie
Responsible Party
Principal Investigator
Principal Investigator

Lidvine Godaert

Doctor

Société Martiniquaise de Gérontologie et Gériatrie

Eligibility Criteria

Inclusion Criteria

  • Age of 75 years or over
  • Admitted to acute care for elders
  • Consent to participate

Exclusion Criteria

  • Impossibility to perform the tests
  • Refusals to participate

Outcomes

Primary Outcomes

Mortality

Time Frame: 6 weeks

Nursing home admission

Time Frame: 6 weeks

Secondary Outcomes

  • Mortality(36 month)
  • Nursing home admission(36 month)

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