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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05128097
Other study ID # 7792
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 1, 2020
Est. completion date December 31, 2021

Study information

Verified date October 2021
Source University Hospital, Strasbourg, France
Contact Emmanuel ANDRES, MD, PhD
Phone 33 3 88 11 50 66
Email emmanuel.andres@chru-strasbourg.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Nowadays, EHPAD residents are polypathological (cognitive and psycho-behavioral pathologies, undernutrition, IC, diabetes, COPD, IR, etc.) and multi-medicated. From a medical point of view, this implies the need for regular monitoring and a high level of medical or even multidisciplinary expertise for the healthcare team. The objective of the GER-e-TEC ™ project is to provide these complex patients with telemedicine tools allowing protocolized and personalized, non-intrusive monitoring. The GER-e-TEC ™ project more specifically takes into account the significant issues in nursing homes of aging residents with the main geriatric syndromes (fall, undernutrition, cognitive-behavioral disorders, iatropathogeny, etc.) The objective of the work undertaken is to develop a codified preventive approach for the management of the main geriatric risks, in order to avoid the occurrence of an acute decompensation factor in the elderly.


Recruitment information / eligibility

Status Recruiting
Enrollment 107
Est. completion date December 31, 2021
Est. primary completion date December 31, 2021
Accepts healthy volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion criteria: - Major subject (=65 years old) - Subject hospitalized between June 17, 2019 to November 13, 2019, in the UF 3723 department, of the Medical Clinic B of the University Hospitals of Strasbourg - Having not expressed his opposition, after information, to the reuse of his data for the purposes of this research. Exclusion criteria: - Subject having expressed opposition to participating in the study - Impossibility of providing the subject with enlightened information (difficulties in understanding the subject, etc.) - Subject under guardianship or guardianship - Subject under safeguard of justice - Subject in palliative / end of life situation - Subject in acute emergency situation

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Médecine interne, Diabète, et Maladies Métaboliques - Hôpitaux Universitaires de Strasbourg Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Retrospective study of the management of the main geriatric risks in the University HÔptaux de Strasbourg Files analysed retrospectively from from June 17, 2019 to November 13, 2019 will be examined]
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