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Impact of a Multifaceted Program to Prevent Postoperative Delirium in the Elderly

CONFUCIUS Study : Impact of a Multifaceted Program to Prevent Postoperative Delirium in the Elderly

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01316965
Acronym
CONFUCIUS
Enrollment
175
Registered
2011-03-16
Start date
2011-04-30
Completion date
2017-05-31
Last updated
2017-05-30

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

Conditions

Postoperative Delirium

Keywords

Postoperative delirium, elderly, prevention, stepped wedge design, healthcare workers

Brief summary

Postoperative delirium is common in the elderly and is associated with a significant increase in mortality, complications, length of hospital stay and admission in long care facility. Several interventions have proved their effectiveness to prevent it but their combination within a multifaceted intervention needs to be assessed using rigorous methodology based on randomized study design. CONFUCIUS trial aims to measure the impact of a multifaceted program on the prevention of postoperative delirium in elderly.

Interventions

BEHAVIORALMultifaceted prevention program HELP(Hospital Elder Life Program)

* A. Structured geriatric consultation will be performed by geriatricians of the MGT(Mobile Geriatric Teams) before surgery, including clinical examination and geriatric assessment * B. All members of medical and nursing staffs will attend a two hours training session performed by the MGTs and HELP(Hospital Elder Life Program) will be implemented in the surgical wards * C. On a quarterly basis, all members of medical and nursing staffs and MGTs will gathered to analyze medical records of patients having experienced a postoperative delirium.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* Male or female subject aged over 75 years * Admission for a scheduled surgery (i.e. all oncologic digestive surgery , ureterostomy, nephrectomy or cystectomy, total hip or knee replacement) * Participation agreement

Exclusion criteria

* Patients with a progressive and/or poorly managed psychiatric pathology (patients with stabilized depression could be included in the study)

Design outcomes

Primary

MeasureTime frame
Postoperative delirium rate within 7 days after surgery7 days after surgery

Secondary

MeasureTime frame
Mean delirium intensity within 7 days after surgery7 days after surgery
Length of hospital stayHospital discharge
Postoperative complications 30 days after surgery incidence30 days after surgery
Mortality 6 months after surgery6 months after surgery
Feasibility of the multidisciplinary prevention program24 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 29, 2026