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Completed

NCT Number: NCT06288295

Retrospective Study on Data Aiming to Establish a Prediction Score for Return Home at the Time of Admission to a Multidisciplinary Medical Department (SCORDOM

The goal of this observational study is to define clinical, biological and socio-cultural criteria, from the very first days of hospitalization on the multidisciplinary medicine department, to guide the patient's discharge from hospital (return to home when discharged from hospital).

The data collected will be those contained in the medical records of patients over 60 years of age who were admitted to the multidisciplinary medical department between October 2021 and February 2022 and between October 2022 and February 2023.

This study also aims at developing and validating a predictive score of orientation at the end of hospitalisation.

Participants are patients previously hospitalized. They will be informed about the study by post and will be able to object to the use of his or her data.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hôpital Privé Nancy Lorraine

Nancy, 54000, France

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

For the development of the score:

  • All patients over 60 years of age admitted to the multidisciplinary medical department in the investigating center between October 2021 and February 2022.
  • Patients for whom data of interest to this study are available in medical records.

For score validation :

  • All patients aged over 60 admitted to the multidisciplinary medicine department of the investigating center between October 2022 and February 2023.
  • Patients for whom data of interest to this study are available in medical records.

Exclusion criteria

  • Patients transferred from an intensive care or continuing care unit
  • Patients in palliative care
  • Patients residing in an EHPAD (establishment for the elderly) or nursing home prior to hospitalization
  • Patients without a minimum blood test on admission (blood test less than 48 hours old)
  • Patients whose reason for hospitalization is due to COVID
  • Patients who have objected to the use of their personal data

Treatment and study plan

Primary outcomes

  1. Number of patients with a return to home after hospitalization and with similar clinical parameters, similar age category, similar pathology and similar biological parameters

    Time frame: Hospital stay, up to 3 weeks

    Data collected among hospital data from october 2021 to february 2022. Clinical parameters measured: age, confusional syndrome, fever, eschar, blood pressure, etc; biological paremeters: (blood test performed in the last 2 days before discharge: albuminemia, natremia, protein C, Creatinemy, hemoglobinemy)

Secondary outcomes

  1. Number of patients with a return to home after hospitalization and with similar clinical parameters, similar age category, similar pathology and similar biological parameters

    Time frame: Hospital stay, up to 3 weeks

    Data collected among hospital data from october 2022 to february 2023. Clinical parameters measured: age, confusional syndrome, fever, eschar, blood pressure, etc; biological paremeters: (blood test performed in the last 2 days before discharge: albuminemia, natremia, protein C, Creatinemy, hemoglobinemy)

Sponsors and collaborators

Lead sponsor

Elsan

Other

Registry information

Official study title

Retrospective Study on Data Aiming to Establish a Prediction Score for Return Home at the Time of Admission to a Multidisciplinary Medical Department

Acronym: SCORDOM

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Mar 1, 2024
Registry last updated
Mar 1, 2024

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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