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Stress Management for Team Coordination
N/A
Waitlist Available
Research Sponsored by Ottawa Hospital Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Timeline
Screening 3 weeks
Treatment Varies
Follow Up through study completion, an average of 1 year
Awards & highlights
Study Summary
This trial explores how stress affects healthcare teams providing high-quality care in emergency situations. It looks at how individual stress impacts team communication, coordination, and performance.
Who is the study for?
This trial is for postgraduate residents and emergency medicine nurses at the University of Ottawa. Participants will be involved in simulation education sessions where they'll face both low and high stress conditions to assess their team coordination and performance.Check my eligibility
What is being tested?
The study tests how teams of healthcare professionals handle simulated emergencies under different levels of stress. It aims to see if stress affects their ability to communicate, make decisions, and work together effectively.See study design
What are the potential side effects?
Since this trial involves psychological stressors rather than medical treatments, traditional side effects are not applicable. However, participants may experience temporary increased stress or anxiety during high-stress simulations.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ through study completion, an average of 1 year
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 1 year
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Team performance
Secondary outcome measures
Frequency of chances between implicit and explicit coordination
Ratio of information management to task management
Team heedfulness score
Other outcome measures
Cognitive appraisal
Heart rate variability - pNN50
Heart rate variability - rMSSD
+1 moreTrial Design
2Treatment groups
Experimental Treatment
Group I: Low-High stress groupExperimental Treatment1 Intervention
Complete the first simulated clinical scenario in the low stress condition, then complete the second simulated scenario in the high stress condition.
Group II: High-Low stress groupsExperimental Treatment1 Intervention
Complete the first simulated clinical scenario in the high stress condition, then complete the second simulated scenario in the low stress condition.
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Who is running the clinical trial?
Ottawa Hospital Research InstituteLead Sponsor
561 Previous Clinical Trials
2,785,583 Total Patients Enrolled
University of OttawaOTHER
205 Previous Clinical Trials
265,983 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:- Not applicable.
Research Study Groups:
This trial has the following groups:- Group 1: Low-High stress group
- Group 2: High-Low stress groups
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Are there any avenues of participation still available for individuals in this experiment?
"Clinicaltrials.gov indicates that this medical research is no longer recruiting subjects, having first been posted on April 1st 2023 and last updated three days later. However, there are presently 137 other clinical trials searching for participants."
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