Clinical Trials Directory

Trials / Recruiting

RecruitingNCT03989245

Measuring the Impact of Care in the Cognitive Behavioural Unit

Status
Recruiting
Phase
Study type
Observational
Enrollment
588 (estimated)
Sponsor
Gérond'if · Academic / Other
Sex
All
Age
70 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to compare the rate of re-hospitalizations in relation to a disruptive behaviour disorder (at 3 and 6 months) between patients who have received care in Cognitive Behavioural Unity (UCC ) and those who have received care in Geriatric Follow-up and Rehabilitation Care Unit (SSR).

Detailed description

The purpose of this muliticentric non-interventional study is to compare the rate of re-hospitalization in relation to a disruptive behaviour disorder between patients receiving care in Cognitive Behavioural Unity UCC (target arm) and those who have received care in Geriatric Care Unit and Rehabilitation SSR (Control arm ). At Inclusion (Month 0) : Inclusion of patients admitted in UCC or in geriatric SSR units for less than 8 days after obtaining of their non opposition. Following data: Socio-educational Level, somatic and psychiatric comorbidities, classification of the type of dementia, evolution of nutritional status, biology (hemoglobin, creatinine, albuminemia), cognitive evaluation, treatment, pain assessment, assessment of disruptive behaviour disorders, discharge modalities, assistance plan, legal protection (before and after hospitalization), types of restraints, measurement of fall rates and their consequences, pathology and/or symptoms observed ( incidents) during hospitalization and vital status will be collected at inclusion and follow-up (1, 3 and 6 months ). At 1 month (M1), exit from hospitalization (M1): Data provided by Investigator . At 3 months (M3) and 6 months (M6) after discharge from hospital in UCC or SSR: Sponsor's Clinical Research Associateall call patient (or his legal representative) or to the primary caregiver or attending physician or EHPAD coordinating physician for collection of questionnaires.

Conditions

Timeline

Start date
2020-01-20
Primary completion
2025-01-01
Completion
2025-12-01
First posted
2019-06-18
Last updated
2024-04-25

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT03989245. Inclusion in this directory is not an endorsement.