Main
|
Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
|
ChiCTR |
Last refreshed on:
|
21 August 2017 |
Main ID: |
ChiCTR-POR-15006944 |
Date of registration:
|
2015-08-21 |
Prospective Registration:
|
Yes |
Primary sponsor: |
|
Public title:
|
A Perioperative Multidisciplinary Intervention to Prevent Postoperative Delirium in Elderly Patients: a Cluster Randomized Controlled Study
|
Scientific title:
|
A perioperative multidisciplinary intervention to prevent postoperative delirium in elderly patients |
Date of first enrolment:
|
2015-09-01 |
Target sample size:
|
Group HELP :119;Control:121; |
Recruitment status: |
Pending |
URL:
|
http://www.chictr.org.cn/showproj.aspx?proj=11685 |
Study type:
|
Prevention |
Study design:
|
Randomized parallel controlled trial
|
Phase:
|
Other
|
|
Countries of recruitment
|
China
| | | | | | | |
Contacts
|
Name:
|
Yanyan Wang
|
Address:
|
37 Guoxuexiang, Chengdu, China
610041
|
Telephone:
|
+86 18140052755 |
Email:
|
Amywyy@126.com |
Affiliation:
|
West China School of Medicine/West China Hospital, SIchuan University |
|
Name:
|
Jirong Yue
|
Address:
|
37 Guoxuexiang, Chengdu, China
610041
|
Telephone:
|
+86 18980601143 |
Email:
|
yuejirong11@hotmail.com |
Affiliation:
|
|
| |
Key inclusion & exclusion criteria
|
Inclusion criteria: 1. Patients aged 70 and older undergoing elective surgery in West China Hospital;
2. Admission to the hospital for at least 2 days;
3. Informed consent and voluntary subjects.
Exclusion criteria: 1. Delirium at baseline, as assessed by the Confusion Assessment Method (CAM);
2. Terminal condition with life expectancy < 6 months;
3. Inability to perform cognitive tests because of legal blindness, severe deafness, or severe dementia;
4. History of schizophrenia or psychosis;
5. Alcohol abuse.
Age minimum:
70
Age maximum:
100
Gender:
Both
|
Health Condition(s) or Problem(s) studied
|
Delirium
|
Intervention(s)
|
Group HELP :HELP intervention protocols;Control:Routine protocol;
|
Primary Outcome(s)
|
Postoperative delirium rate within 7 days after surgery;
|
Secondary Outcome(s)
|
Mean delirium severity;Delirium duration;Length of hospital stay;Cognitive function decline;Physical function decline;Frailty index;Postoperative complications after surgery;Patients Cost;
|
Source(s) of Monetary Support
|
MILSTEIN MEDICAL ASIAN AMERICAN Partnership Foundation
|
Results
|
Results available:
|
|
Date Posted:
|
|
Date Completed:
|
|
URL:
|
|
|
|