- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04177589
Incidence of Delirium in Inpatient Elderly Patients
Incidence of Delirium and Some Related Factors in Elderly Patients Hospitalized in Geriatrics Department, Gia Dinh Hospital.
Study: prospective cohort study Register for research topic on ClinicalTrails.gov. Convenience sampling, all patients aged 60 and older entered the geriatric department of Gia Dinh People's Hospital in Ho Chi Minh City from December 2020 to May 2021.
Direct interview with the patient. Minimum time 10-15 minutes for each interview.
Evaluation at the time of admission (within the first 24 hours of admission): demographic characteristics, diagnosis at Geriatric ward, frailty, activities of daily living.
Assessment during hospital stay: identifying delirum using the CAM tool. Assessment at the time of discharge: diagnosis at discharge and the drugs used during inpatient treatment in the department.
Research objectives:
- Determine the incidence of delirium in elderly patients in general geriatric department.
- Investigate some of the important related factors that are common for delirium in elderly patients in general geriatric department.
- Determine the relationship between delirium and clinical outcomes in elderly patients in general geriatric department.
Study Overview
Status
Intervention / Treatment
Detailed Description
Study design: prospective cohort study. Time: From December 2020 to May 2021. Place: Department of Geriatrics, Gia Dinh People's Hospital, Ho Chi Minh City. Sample population: All patients aged 60 and older entered the Geriatric Department of Gia Dinh People's Hospital in Ho Chi Minh City from December 2020 to May 2021.
Sampling technique: Convenience sampling Admission criteria: All patients ≥ 60 years of age agree to participate in the study.
Exclusion criteria: Disturbance or other cognitive disorders at the time of assessment at admission, hospital stay not exceeding 48 hours
Data collection:
Data collection process:
Direct interview with the patient. Minimum time 10-15 minutes for each interview (excluding time to explain purpose, method of conducting research, time for collecting information on demographic characteristics and medical conditions).
Person doing interview: geriatric resident doctors including Dinh Pham Thi Thuy Van, Huynh Khoi Nguyen, Tran Tan Dat The interviewers will explain the research objectives and only started conducting the interview when the patient or his relative (authorized) agreed to participate in the study.
Conduct interviews:
*Evaluation at the time of admission (within the first 24 hours of admission): Patients entering the geriatric ward who agree to participate in the study will be assessed by the doctor for cognitive status, clinical characteristics and a diagnostic flow chart for Delirium
Record details about:
- Demographic characteristics: gender, age, address, occupation, family status and marital status.
- Diagnosis at the time of admission, co-morbidities (pulmonary disease, hypertension, type 2 diabetes, chronic kidney disease, osteoporosis, osteoarthritis, constipation, liver and gastrointestinal diseases, cardiovascular disease, arrhythmia, endocrine and metabolic disorders, neurological diseases, urological diseases, hematological pathologies and other diseases). Amount and type of medication being taken at home up to the time of admission. Routine tests.
Frailty status, functional activities according to ADLs and IADLs scale, initial cognitive status according to MMSE, vision and hearing.
- Evaluation during the hospital stay:
When a patient is suspected of delirium, we evaluate it using the CAM tool to identify. After that, the patient was recorded the following characteristics: the time of onset, the clinical form (increased activity, decreased activity or mixed), current medical conditions and medications.
Record falls, transfer to other wards (if any).
*Evaluation at the time of discharge: At the time of discharge, we will record the time of hospitalization, the reason for discharge (improved condition or relative request due to serious illness) or the place of hospital transfer or in-hospital death (if any).
Record diagnosis on discharge and drugs used during inpatient treatment at the department
Data collection tools: A sheet of prepared data and medical records.
Bias control:
Information discrepancy
- Clearly define the subjects of study.
- Choose a sample according to admission and exclusion criteria
Selection errors
- The person doing the interview is the person who wrote the data collection sheet, so it will limit the errors in the interview process.
- The variables are clearly defined and measurable.
- Collect information in a unified form.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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-
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Ho Chi Minh City, Vietnam, 700000
- Department of Geriatrics, Gia Dinh People's Hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- All patients ≥ 60 years of age agree to participate in the study.
Exclusion Criteria:
- Disturbance or other cognitive disorders at the time of assessment at admission, hospital stay not exceeding 48 hours
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Incidence of Delirium in Inpatient Elderly Patients
Time Frame: from December 2020 to May 2021
|
Incidence of Delirium in elderly patients entered the Geriatric Department of Gia Dinh People's Hospital in Ho Chi Minh City
|
from December 2020 to May 2021
|
Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- NTL
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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