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OpenTrials
Completed

NCT Number: NCT01699984

PERDOVE ANZIANI: a Prospective Cohort Study on Older Patients

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.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

IRCCS Centro San Giovanni di Dio Fatebenefratelli, Brescia, Italy

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • age 65 or older
  • informed consent provided

Exclusion criteria

  • younger than 65 years
  • informed consent not provided

Treatment and study plan

Primary outcomes

  1. evaluation of clinical improvement

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

Secondary outcomes

  1. identification of variables predictive of outcomes

    Time frame: at discharge (or 3 months after admission) and 6 months follow-up

Other outcomes

  1. evaluation of predictive abilities of clinicians

    Time frame: admission, discharge (or 3 months of hospitalization) and 6 months follow-up

Sponsors and collaborators

Lead sponsor

IRCCS Centro San Giovanni di Dio Fatebenefratelli

Other

Registry information

Official study title

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

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
Oct 4, 2012
Registry last updated
Oct 4, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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