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Trial registered on ANZCTR
Registration number
ACTRN12609000180213
Ethics application status
Approved
Date submitted
25/11/2008
Date registered
17/04/2009
Date last updated
9/06/2011
Type of registration
Retrospectively registered
Titles & IDs
Public title
A pilot study to monitor light exposure and sleep wake cycles in post-operative cardiac patients and its implications for hospital stay and depression.
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Scientific title
A pilot study to monitor light exposure and sleep wake cycles in post-operative cardiac patients and its implications for hospital stay and depression.
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Secondary ID [1]
262347
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No Secondary ID
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Light exposure in the hospital environment
4017
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Condition category
Condition code
Other
4222
4222
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0
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Conditions of unknown or disputed aetiology (such as chronic fatigue syndrome/myalgic encephalomyelitis)
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Patients have their light exposure and activity levels monitored using actigraphy and daysimetry. Patients are asked to wear both items from the evening following cardiac surgery until their discharge from hospital. Actiwatches and daysimeters both measure light levels as well as measuring rest-activity rhythms. One sits on the wrist and one on the ear. The concept is that they will hav differing results for the same patient due to their positioning.
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Intervention code [1]
3741
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Not applicable
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Comparator / control treatment
No control - validation study of the two different types of equipment. The study compares the well validated and more commonly used actigraphy (actiwatch on the wrist) with a newer device which is thought to be more useful due to its ideal positioning close to the retina.
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Light exposure in hospital environment measured using two methods of measurement, actigraphy is a validated method of light and activity measurement. Daysimetry results will then be correlated with the actigraphy results.
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Assessment method [1]
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Timepoint [1]
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Light exposure and activity levels measured throughout their hospital stay, starting immediately post-surgery
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Secondary outcome [1]
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Mood disruption measured using a questionnaire
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Assessment method [1]
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Timepoint [1]
8609
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Mood is measured using a questionnaire administered pre-surgery and on the last day of hospitalisation. Questionnaires used: Hamilton Depression Scale, Beck Depression Questionnaire, Hospital Anxiety and Depression Scale, Profile of Mood States.
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Eligibility
Key inclusion criteria
Patients must be scheduled for cardiac surgery
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Minimum age
18
Years
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Maximum age
Not stated
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
Any condition which may put the patient at risk by participating or any condition which may cause confounding of results
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Study design
Purpose
Psychosocial
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Duration
Cross-sectional
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Selection
Defined population
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
1/12/2008
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
20
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Accrual to date
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Final
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Recruitment outside Australia
Country [1]
1403
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New Zealand
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State/province [1]
1403
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Funding & Sponsors
Funding source category [1]
4203
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Self funded/Unfunded
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Name [1]
4203
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University of Auckland
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Address [1]
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7 Symonds St
Auckland Central
1010
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Country [1]
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New Zealand
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Primary sponsor type
University
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Name
University of Auckland
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Address
7 Symonds St
Auckland Central
1010
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Country
New Zealand
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
3776
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Country [1]
3776
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Ethics approval
Ethics application status
Approved
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Summary
Brief summary
Hospitals are characterized by their lack of strong daily light-dark cycles. Light levels in the intensive care unit and ward are generally much lower than normal during the day and higher than normal at night. Appropriately timed administration of bright light has been shown to be highly effective in entraining the circadian clock, improving sleep timing and mood of depressed patients in other clinical settings. In this study we aim to investigate the validity of a novel head worn device for the measurement of light exposure and sleep/ wake cycles in post-operative cardiac patients. Subjects will be asked to wear a wrist worn actimeter with an integrated light sensor and a head worn daysimeter (incorporating light and activity sensors). Data from this pilot study will for the first time provide accurate assessments of eye level light exposures in post-operative patients. Simultaneous monitoring of mood will also enable the determination of the influence of light exposure on post-operative depression.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Anisoara Jardim
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Address
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98 Mountain Rd
Epsom
Auckland
1024
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Country
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New Zealand
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Phone
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+64 21 705562
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Anisoara Jardim
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Address
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98 Mountain Rd
Epsom
Auckland
1024
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Country
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New Zealand
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Phone
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+64 21 705562
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Fax
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Email
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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