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Main
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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. |
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Register:
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TCTR |
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Last refreshed on:
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29 April 2024 |
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Main ID: |
TCTR20170330001 |
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Date of registration:
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30/03/2017 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Bright Light Therapy for prevention of delirium in patients at Surgical Intensive Care Unit in King Chulalongkorn Memorial Hospital.
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Scientific title:
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Bright Light Therapy for prevention of delirium in patients at Surgical Intensive Care Unit in King Chulalongkorn Memorial Hospital. |
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Date of first enrolment:
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01/09/2016 |
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Target sample size:
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Recruitment status: |
Completed |
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URL:
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https://www.thaiclinicaltrials.org/show/TCTR20170330001 |
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Study type:
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Interventional |
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Study design:
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Randomized
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Phase:
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N/A
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Countries of recruitment
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Thailand
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Contacts
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Name:
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Sirimas
Potharajaroen |
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Address:
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1873 King Chulalongkorn Memorial Hospital Rama IV road. Bangkok
10330
Bangkok
Thailand |
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Telephone:
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0879966631 |
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Email:
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puiphay_moomoo@hotmail.com |
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Affiliation:
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Department of Psychiatry, Faculty of Medicine, Chulalongkorn University |
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Name:
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Sirimas
Potharajaroen |
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Address:
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1873 King Chulalongkorn Memorial Hospital Rama IV road. Bangkok
10330
Bangkok
Thailand |
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Telephone:
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0879966631 |
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Email:
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puiphay_moomoo@hotmail.com |
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Affiliation:
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Department of Psychiatry, Faculty of Medicine, Chulalongkorn University |
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Key inclusion & exclusion criteria
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Inclusion criteria: age ≥ 50 years, both sexes, understand Thai language, APACHE II Score ≥ 8, post-operation and admitted to the SICU
Exclusion criteria: no history of delirium, brain diseases or dementia, Psychiatric illness, memory problems, coma, can not sit in 30 degree or 45 degree (for example due to c-spine injury), had eye problems such as had allergic of bright light, Glaucoma and Diabetic Retinopathy.
Age minimum:
50 Years
Age maximum:
100 Years
Gender:
Both
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Health Condition(s) or Problem(s) studied
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patient denied
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Intervention(s)
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Intervention group ,Control group
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Experimental Device,No Intervention No treatment
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Intervention group had bright light therapy 5,000 lx for 2 hrs. at 09.00-11.00 am after admission within the first 24 hrs SICU admission and had usual care.,control group had light 500-600 lx and had usual care.
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Primary Outcome(s)
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bright light reduce delirium 3 days questionnaire
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Secondary Outcome(s)
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bright light reduce insomnia 3 days questionnaire
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Source(s) of Monetary Support
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Chulalongkorn University Scholarship
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Ethics review
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Status: Submitted, approved
Approval date:
Contact:
Ethics Committees Faculty of Medicine, Chulalongkorn University
022564493 Ext.
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Results
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Results available:
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Date Posted:
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Date Completed:
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31/03/2017 |
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URL:
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