- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07920627
Epidemiology of Clostridioides Difficile Infection (CDI) in Long-term Care Facilities, Assessment of Professional Practices Related to CDI Risk Prevention, and Strategies for Improving Care. (EpiCE)
Clostridioides difficile infection (CDI) is the leading cause of infectious diarrhea among older adults. The epidemiology of community-acquired CDI, particularly among residents of long-term care facilities, remains poorly understood to this day. While numerous studies on the epidemiology, prevention, diagnosis, and treatment of CDI have been conducted in hospital settings, primary care often lags behind these advances. Limited access to diagnostic tests and treatment options, as well as insufficient resources allocated to preventing cross-transmission, are all factors that hinder the control of ICD in long-term care facilities. This will be the first French study on the epidemiology of ICD among nursing home residents, which can serve as a reference for implementing a multidisciplinary action plan and measuring its impact. This will be carried out as part of a city-hospital collaboration and will facilitate the creation of a healthcare network involving multiple healthcare providers, such as general practitioners working in nursing homes, clinical laboratories, pharmacies, dietitians and nutritionists, and the university hospital.
A better understanding of the epidemiology of ICD among residents in long-term care facilities and an assessment of professional practices related to ICD risk prevention should enable us to better target strategies for improving care while raising awareness among healthcare providers and public health policymakers. We therefore plan to optimize the impact of implementing a multidisciplinary action program aligned with the expectations of frontline practitioners regarding the reduction of the risk of ICD (training, prevention tools, diagnosis and treatment of ICD, appropriate use of antibiotics, nutritional counseling, prescribing probiotics, and establishing a coordinated care pathway for ICD). The implementation of this action program is expected to reduce the incidence rate of ICD, the recurrence rate, and antibiotic use in nursing homes, as well as the number of transfers to the hospital for ICD management.
Studieöversikt
Status
Betingelser
Studietyp
Inskrivning (Beräknad)
Kontakter och platser
Studieorter
-
-
-
Marseille, Frankrike
- Assistance Publique Hopitaux de Marseille
-
-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Testmetod
Studera befolkning
residents of nursing homes
Beskrivning
Inclusion Criteria:
- Men or women aged 65 or older
- Patients who have received information about the study and have not expressed objection
- Residents of the nursing home for more than 72 hours during the 12-month enrollment period
- No objection to the use of clinical and biological data in the event of an ICD.
Exclusion Criteria:
- A patient who is in the exclusion period of another research protocol at the time the informed consent form is obtained.
- A person who does not understand French
- No inclusion criteria.
Studieplan
Hur är studien utformad?
Designdetaljer
- Observationsmodeller: COHORT
- Tidsperspektiv: PROSPECTIVE
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
Incidence Rate of ICD
Tidsram: 24 MONTHS
|
|
24 MONTHS
|
Sekundära resultatmått
Resultatmått |
Tidsram |
|---|---|
|
the recurrence rate of C. difficile colitis
Tidsram: 24 MONTHS
|
24 MONTHS
|
|
Measuring the Use of Critical Antibiotics
Tidsram: 24 MONTHS
|
24 MONTHS
|
|
Measure the number of hospital transfers for ICD management.
Tidsram: 24 MONTHS
|
24 MONTHS
|
|
the prevalence of the main risk factors for ICD
Tidsram: 24MONTHS
|
24MONTHS
|
Samarbetspartners och utredare
Utredare
- Huvudutredare: cassir nadim, assistance publique hôpitaux de Marseille
Studieavstämningsdatum
Studera stora datum
Studiestart (Beräknad)
Primärt slutförande (Beräknad)
Avslutad studie (Beräknad)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- RCAPHM26_0189
- PADS26-262 (Annan identifierare: APHM)
Läkemedels- och apparatinformation, studiedokument
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