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Stress Resilience Training for Nurse Burnout
N/A
Waitlist Available
Led By Soo-Jeong Lee
Research Sponsored by University of California, San Francisco
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 baseline to immediately post-esrt intervention; baseline to 1 month after esrt intervention; baseline to 3 months after esrt intervention th, and 3-month after the 5-week esrt
Awards & highlights
Study Summary
This trial examines the effects of a 5-week intervention to improve psychosocial and occupational well-being of critical care nurses, reducing burnout and increasing stress resilience.
Who is the study for?
This trial is for adult critical care nurses working at UCSF Health who are experiencing job stress and burnout. Participants must be able to attend all five sessions of the Enhanced Stress Resilience Training (ESRT). Travel nurses or those unable to commit fully are excluded.Check my eligibility
What is being tested?
The study tests the effectiveness of a 5-week Enhanced Stress Resilience Training program aimed at improving stress management, emotional well-being, and job performance among critical care nurses. It's a randomized trial with some participants on a waitlist as control.See study design
What are the potential side effects?
Since ESRT is a training intervention focused on stress management techniques rather than medication, it does not have traditional side effects. However, individuals may experience varying levels of emotional discomfort during the process.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline to immediately post-esrt intervention; baseline to 1 month after esrt intervention; baseline to 3 months after esrt intervention 3-month after the 5-week esrt
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline to immediately post-esrt intervention; baseline to 1 month after esrt intervention; baseline to 3 months after esrt intervention 3-month after the 5-week esrt
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Changes in burnout score
Secondary outcome measures
Changes in depressive symptom score
Changes in mindfulness score
Changes in perceived stress score
+6 moreOther outcome measures
ESRT acceptability scores
Percentage of participants in each ESRT session
The frequency of ESRT skill use (ESRT sustainability)
Trial Design
2Treatment groups
Experimental Treatment
Group I: Waitlist ControlExperimental Treatment1 Intervention
The control group will receive ESRT after the intervention group finishes the 5-week ESRT program.
Group II: ESRT InterventionExperimental Treatment1 Intervention
Five 1-hour weekly ESRT sessions
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Who is running the clinical trial?
University of California, San FranciscoLead Sponsor
2,507 Previous Clinical Trials
15,238,527 Total Patients Enrolled
Soo-Jeong LeePrincipal InvestigatorUniversity of California, San Francisco
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: ESRT Intervention
- Group 2: Waitlist Control
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 new patients still being enrolled for this research?
"Indeed, the clinicaltrials.gov records show that this trial is currently seeking patients to enrol in the study. It was originally posted April 25th 2023 and has recently been updated on June 6th 2023; it seeks a total of 100 participants from one medical site."
Answered by AI
How many participants are qualifying for this trial?
"Correct. According to clinicaltrials.gov, this medical research project which was first uploaded on April 25th 2023 is currently recruiting participants. 100 people are needed from 1 facility for the duration of the trial."
Answered by AI
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