The purpose of the study is to determine if temporarily relocating clinicians who deliver remote care using the eICU telehealth system to Sydney, Australia will lead to greater job satisfaction, reduced physiologic stress, and improve performance. Four nurses and six physicians will be sent to a site in Sydney Australia on a rotating basis to determine whether providing care during the Australian daytime is more efficient and precise than providing care during the night in the United States.
The purpose of the study is to determine if temporarily relocating clinicians who deliver remote care using the eICU telehealth system to Sydney Australia will lead to greater job satisfaction, reduced physiologic stress, and improve performance. Four nurses and six physicians will be sent to a site in Sydney Australia on a rotating basis to determine whether providing care during the Australian daytime is more efficient and precise than providing care during the night in the United States. As part of this pilot, each participant will undergo a series of evaluations before leaving, while in Australia, and after returning. The evaluations will include questionnaires related to well-being, task assessment (such as completing a paper maze or performing arithmetic), physiology assessment (such as continuous measure of heart rate by a wristwatch type device), and stress assessment (by sampling saliva and measuring cortisol and interleukin-1 Beta). The researchers would like to determine whether normalization of the provider's (physician or nurse who are the research subjects) sleep-wake cycle improves subjective and objective well-being. Additionally, investigators seek to determine whether normalization of the provider's (physician or nurse who are the research subjects) sleep-wake cycle improves alertness and focus, and determine whether normalization of the provider's (physician or nurse who are the research subjects) sleep-wake cycle improves job performance.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Enrollment
7
Clinical Operations Room (COR) staff will travel to Sydney Australia to deliver telehealth to patients in Georgia United States. Upon arrival, participants will have eight nights and seven days free of clinical responsibilities. Thereafter, each participant will work four consecutive days of 12 hour shifts followed by four consecutive days with no clinical assignment. The following week, participants will work three consecutive days of 12 hour shifts followed by four consecutive days with no clinical assignment. Upon return to the USA, participants will have a week free of clinical responsibilities.
Emory University
Atlanta, Georgia, United States
Change in Salivary Cortisol Levels
Saliva will be collected via a mouth swab and tested for cortisol levels. Cortisol is a stress biomarker.
Time frame: Baseline, Post Intervention (Up to 8 weeks)
Change in Stanford Sleepiness Scale Score
The Stanford Sleepiness Scale is a seven point scale that asks participants to assess how alert they are feeling throughout the day. A result of 4 or below may indicate that a participant could be suffering from a lack of sleep
Time frame: Baseline, Post Intervention (Up to 8 weeks)
Change in the Trail Making Test A Score
During the Trail Making Test A, participants will be asked to draw lines to connect circled numbers in a numerical sequence (i.e., 1-2-3, etc.) as rapidly in possible. A shorter time indicates better cognition.
Time frame: Baseline, Post Intervention (Up to 8 weeks)
Change in the Trail Making Test B Score
During the Trail Making Test B, participants will be asked to draw lines to connect circled numbers and letters in an alternating numeric and alphabetic sequence (i.e., 1-A-2-B, etc.) as rapidly as possible. A shorter time indicates better cognition.
Time frame: Baseline, Post Intervention (Up to 8 weeks)
Change in Physical Activity assessed by Multi-Scale Entropy
Multi-scale entropy will be measured using a Jawbone wristband device provided to participants upon enrollment.
Time frame: Baseline, Post Intervention (Up to 8 weeks)
Change in Physical Activity assessed by Multi-Scale Complexity
Multi-scale complexity will be measured using a Jawbone wristband device provided to participants upon enrollment.
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Time frame: Baseline, Post Intervention (Up to 8 weeks)
Change in Heart Rate Variability assessed by Deceleration Capacity
Deceleration capacity will be measured using a Jawbone wristband device provided to participants upon enrollment.
Time frame: Baseline, Post Intervention (Up to 8 weeks)
Change in Heart Rate Variability assessed by Acceleration Capacity
Acceleration capacity will be measured using a Jawbone wristband device provided to participants upon enrollment.
Time frame: Baseline, Post Intervention (Up to 8 weeks)
Frequency of Arrhythmias
The frequency of arrhythmias will be collected using a Jawbone wristband device provided to participants upon enrollment.
Time frame: Duration of Study (Up to 31 Days)
Change in Sleep Latency
Sleep latency is the length of time it takes to accomplish the transition from full wakefulness to sleep. This will be measured in minutes using a Jawbone wristband device provided to participants upon enrollment.
Time frame: Baseline, Post Intervention (Up to 8 weeks)
Number of Awakenings per Hour
The number of times a participants awakes during sleep will be monitored at every hour using a Jawbone wristband device provided to participants upon enrollment.
Time frame: Duration of Study (Up to 31 Days)
Change in Percent of Non Rapid Eye Movement (REM) Sleep
Change is the difference between the percentage of non REM sleep taken during performance phases.
Time frame: Baseline, Post Intervention (Up to 8 weeks)
Change in Mood Symptom Questionnaire Score
The Mood Symptom Questionnaire was originally designed to diagnose bipolar disorder. The questionnaire takes about five minutes to complete, and can provide important insights into diagnosis and treatment.If the patient answers "Yes" to seven or more of the 13 items in question number 1 AND "Yes" to question number 2 AND "Moderate" or "Serious" to question number 3, there is a positive screen.
Time frame: Baseline, Post Intervention (Up to 8 weeks)
Change in Patient Health Questionnaire-9 (PHQ-9) Score
The PHQ-9 is a multi-purpose instrument for screening, diagnosing, monitoring, and measuring the severity of depression. A score of 5-9 represents signs of minimal depression symptoms. A score of 10-14 represents symptoms of minor depression. A score of 15-19 represents symptoms of major depression, moderately severe. A score of greater than 20 represents symptoms of major depression, severe.
Time frame: Baseline, Post Intervention (Up to 8 weeks)
Change in Number of Camera Sessions
Difference in the number of camera sessions completed during performance phases.
Time frame: Day 1, Day 31
Change in Duration of Camera Sessions
Difference in the duration of camera sessions during performance phases measured in minutes.
Time frame: Day 1, Day 31
Change in Urgency of Clinical Contacts
Difference in priority levels assigned to each clinical contact (levels: preventative; informative/procedural; urgent; life-threatening)
Time frame: Day 1, Day 31
Change in Number if Clinical Record Entries
Difference in the number of clinical record entries made by physicians only during the performance phases.
Time frame: Day 1, Day 31
Change in Duration of Service
Difference in the duration of physician services during each performance phase measured in hours.
Time frame: Day 1, Day 31