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Clinical Trials/NCT01699984
NCT01699984
Completed
N/A

THE HOSPITALIZATION OF OLDER PATIENTS: RISK FACTORS, ADVERSE EVENTS AND OUTCOMES. A MULTICENTRE STUDY.

IRCCS Centro San Giovanni di Dio Fatebenefratelli4 sites in 1 country329 target enrollmentFebruary 2011

Overview

Phase
N/A
Intervention
Not specified
Conditions
Dementia
Sponsor
IRCCS Centro San Giovanni di Dio Fatebenefratelli
Enrollment
329
Locations
4
Primary Endpoint
evaluation of clinical improvement
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

This prospective observational cohort study aims at studying functional and clinical outcomes of patients (N = 329) admitted to 4 geriatric hospital facilities of the St John of God Order in Northern Italy during an index period of 4 months. Other areas assessed include variables that help or hinder the discharge of patients with sufficient residential autonomy and the predictive ability of clinicians compared with the evaluation of selective indicators of outcome (clinical and instrumental).

Patients are followed from the first day of hospitalization until discharge or up to 3 months and 1 day after the date of admission ("long-term care" patients).

At admission a "Patient Form" including social, demographic and clinical informations and a series of standardized assessment tools is completed with the help of clinicians, nurses and caregivers (when available).

For each patient, during hospitalization, an analysis of apolipoprotein ApoE polymorphisms is performed and adverse events occurred during hospitalization are monitored, as well as the predictive abilities of clinicians and any recent CT and MRI. Patients are reassessed at discharge (or after 3 months for "long-term care" patients) and at 6 months follow-up of with a standardized telephone interview to assess clinical and functional status and possible changes in the residential status of the patient.

Registry
clinicaltrials.gov
Start Date
February 2011
End Date
September 2012
Last Updated
13 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
IRCCS Centro San Giovanni di Dio Fatebenefratelli
Responsible Party
Principal Investigator
Principal Investigator

Giovanni de Girolamo, M.D.

M.D., Scientific Director

IRCCS Centro San Giovanni di Dio Fatebenefratelli

Eligibility Criteria

Inclusion Criteria

  • age 65 or older
  • informed consent provided

Exclusion Criteria

  • younger than 65 years
  • informed consent not provided

Outcomes

Primary Outcomes

evaluation of clinical improvement

Time Frame: from admission to discharge (or after 3 months of hospitalization) and 6 months follow-up

Secondary Outcomes

  • identification of variables predictive of outcomes(at discharge (or 3 months after admission) and 6 months follow-up)

Study Sites (4)

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