← Back to Search

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 weeks
Treatment ~ Varies
Follow Up ~through study completion, an average of 1 year
This trial's timeline: 3 weeks for screening, Varies for treatment, and through study completion, an average of 1 year for reporting.

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 more

Trial 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.

Find a Location

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

Media Library

Low-High stress group Clinical Trial Eligibility Overview. Trial Name: NCT05798052 — N/A
Stress Research Study Groups: Low-High stress group, High-Low stress groups
Stress Clinical Trial 2023: Low-High stress group Highlights & Side Effects. Trial Name: NCT05798052 — N/A
Low-High stress group 2023 Treatment Timeline for Medical Study. Trial Name: NCT05798052 — N/A

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."

Answered by AI
~54 spots leftby Apr 2025