Delirium Clinical Trial
Official title:
Usefulness of Bright Light Therapy in the Prevention of Delirium in Patients Undergoing Hematopoietic Stem Cell Transplant (HSCT)
The purpose of this study is to find out if using bright light sessions during bone marrow transplant can prevent people from developing confusion also known as delirium.
Status | Recruiting |
Enrollment | 90 |
Est. completion date | April 2014 |
Est. primary completion date | April 2014 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 90 Years |
Eligibility |
Inclusion Criteria: - 18 or older - Male or female - Patients scheduled to undergo HSCT - English speaking Exclusion Criteria: - Previous history of bipolar affective disorder - On-going delirium - History of substance abuse/dependence within 6 months prior to HSCT - History of invasive melanoma. Patients with a history of basal cell carcinoma, melanoma in situ, or squamous cell carcinoma are permitted to enroll if the lesion(s) have been excised with negative margins - History of medical/dermatological conditions that make skin especially sensitive to light,such as systemic lupus erythematosus (SLE) and/or porphyria - Eye condition that makes eyes vulnerable to light damage - Concomitant use of medications that increase sensitivity to sunlight, such as the herbal supplement St. John's Wort - Established primary insomnia |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Outcomes Assessor), Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
United States | Massachusetts General Hospital | Boston | Massachusetts |
Lead Sponsor | Collaborator |
---|---|
Massachusetts General Hospital | American Cancer Society, Inc. |
United States,
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* Note: There are 27 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Incidence of delirium (Time to the development of delirium based on meeting criteria on the Delirium Rating Scale and/or Memorial Delirium Assessment Scale) | Monday, Wednesday, and Friday assessments will begin after beginning light therapy and include the Delirium Rating Scale-Revised-98 (DRS-98)and Memorial Delirium Assessment Scale (MDAS) | From hospital admission until the date of first documented delirium, assessed up to 28 days post-transplant | No |
Secondary | Length and severity of delirium episodes | Monday, Wednesday, and Friday assessments include the Delirium Rating Scale-Revised-98 (DRS-98)and Memorial Delirium Assessment Scale (MDAS); Patients will receive assessments after beginning light therapy until day 28 post-transplant or discharge, whichever comes first. | From first documented episode of delirium until discharge from the hospital, assessed up to 28 days post-transplant | No |
Secondary | Average dose of antipsychotic medications required to manage delirium | From admission to hospital to discharge, an expected average of 28 days post-transplant | No | |
Secondary | Hospital length of stay | From admission to hospital to discharge, an expected average of 28 days post-transplant | No | |
Secondary | Complications (falls, aspiration, infections, nutritional deficits) | Available and pertinent laboratory data will be collected including serum electrolytes, serum BUN, serum creatinine, TSH, LFTs, CBC with differential, Alkaline phosphatase and urinalysis. These tests are performed as part of routine clinical care on patients undergoing HSCT. | From admission to hospital to discharge, an expected average of 28 days post-transplant | No |
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