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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06288295
Acronym
SCORDOM
Enrollment
600
Registered
2024-03-01
Start date
2021-10-01
Completion date
2023-02-28
Last updated
2024-03-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Continuity of Patient Care

Keywords

predictive score, return to home, elderly

Brief summary

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.

Interventions

None listed

Sponsors

Elsan
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
No

Inclusion criteria

For the development of the score: 1. All patients over 60 years of age admitted to the multidisciplinary medical department in the investigating center between October 2021 and February 2022. 2. Patients for whom data of interest to this study are available in medical records. For score validation : 1. All patients aged over 60 admitted to the multidisciplinary medicine department of the investigating center between October 2022 and February 2023. 2. Patients for whom data of interest to this study are available in medical records.

Exclusion criteria

1. Patients transferred from an intensive care or continuing care unit 2. Patients in palliative care 3. Patients residing in an EHPAD (establishment for the elderly) or nursing home prior to hospitalization 4. Patients without a minimum blood test on admission (blood test less than 48 hours old) 5. Patients whose reason for hospitalization is due to COVID 6. Patients who have objected to the use of their personal data

Design outcomes

Primary

MeasureTime frameDescription
Number of patients with a return to home after hospitalization and with similar clinical parameters, similar age category, similar pathology and similar biological parametersHospital stay, up to 3 weeksData 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

MeasureTime frameDescription
Number of patients with a return to home after hospitalization and with similar clinical parameters, similar age category, similar pathology and similar biological parametersHospital stay, up to 3 weeksData 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)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026