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STRIVE Group for Stress

N/A
Recruiting
Research Sponsored by Lawson Health 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 3 months
Awards & highlights

Study Summary

This trial aims to see if formal resilience training can improve self-reported resilience scores in junior physicians-in-training. They will also assess if the timing of the training (first vs second year of residency) makes

Who is the study for?
This trial is for first- and second-year medical residents at the Schulich School of Medicine & Dentistry, specifically in Anesthesia and Emergency Medicine programs. It's open to all eligible residents regardless of age, gender, health status, or race.Check my eligibility
What is being tested?
The STRIVE trial is testing whether a formal resilience training program can boost self-reported resilience scores among junior physicians-in-training compared to usual resources on resilience. The effect of training timing will also be assessed.See study design
What are the potential side effects?
Since this intervention involves educational content rather than medication or procedures, traditional physical side effects are not expected. However, participants may experience varying psychological impacts from the training.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and 3 months for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
To evaluate of the effect of formal resilience training using the STRIVE course on self-reported resilience at 3 months.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: STRIVE GroupExperimental Treatment1 Intervention
STRIVE is comprised of a 4-hour formal education session where participants are provided knowledge, skills, and resources specific to self-assessment for mental wellness and effective mindfulness strategies. High-fidelity simulation sessions are utilised to reinforce and apply mindfulness techniques learned in the formal session. Clinical scenarios are designed to be challenging and stressful.
Group II: ControlActive Control1 Intervention
Residents randomized to the control group will receive information regarding resilience development as per the usual standard of communication. All new residents will receive contact details of physician wellness services available at Schulich School of Medicine & Dentistry.

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Who is running the clinical trial?

Lawson Health Research InstituteLead Sponsor
659 Previous Clinical Trials
413,678 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Is the enrollment for this medical study currently accepting new participants?

"Affirmative. Data on clinicaltrials.gov indicates that this investigation is currently seeking volunteers. It was initially posted on April 4th, 2023 and most recently revised on February 26th, 2024. The aim is to recruit 54 participants from a single site."

Answered by AI

How many individuals are currently enrolled as participants in this clinical trial?

"Affirmative, information from clinicaltrials.gov indicates that this study is actively seeking suitable candidates. This trial was initially posted on April 4th, 2023 and last revised on February 26th, 2024. The aim is to recruit a total of 54 participants at one designated site."

Answered by AI
~20 spots leftby Dec 2024