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Behavioral Intervention
Online Coaching for Burnout
N/A
Recruiting
Led By Zahidee (Saidie) Rodriguez, MD
Research Sponsored by Emory University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 month or 9 months
Awards & highlights
Study Summary
This trial will assess if online coaching can help reduce burnout in APPs by providing support and guidance.
Who is the study for?
This trial is for nurse practitioners, physician assistants, clinical nurse specialists, and certified registered nurse anesthetists at CHOA, Emory University, CU and affiliates. It includes pregnant women but excludes those who can't consent, are not adults or prisoners, have cognitive impairments or don't understand English.Check my eligibility
What is being tested?
The study tests if online coaching can reduce burnout in advanced practice providers. Participants will receive either usual treatment or join a hybrid coaching program involving video sessions, written materials and self-coaching tools.See study design
What are the potential side effects?
Since this trial involves non-medical interventions like coaching programs rather than drugs or medical procedures, traditional side effects are not expected; however participants may experience stress or discomfort from discussing personal issues.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 month or 9 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 month or 9 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Change in Burnout
Change in the percentage of participants that accept the program course
Change in the percentage of participants that complete >50% of self-study worksheets
+3 moreSecondary outcome measures
Change in Loneliness
Change in Moral Injury
Change in Self Reflection and Insight Scale
+4 moreTrial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Group Coaching ProgramExperimental Treatment1 Intervention
The study intervention is a hybrid asynchronous-synchronous group coaching treatment that will occur over four months. Participants will be given access to a members-only, web-based platform to access the intervention.
Group II: Usual TreatmentPlacebo Group1 Intervention
This group will participate in the study intervention following a 4-month waitlist/control group.
Find a Location
Who is running the clinical trial?
University of Colorado, DenverOTHER
1,738 Previous Clinical Trials
2,149,226 Total Patients Enrolled
Emory UniversityLead Sponsor
1,640 Previous Clinical Trials
2,560,357 Total Patients Enrolled
Children's Healthcare of AtlantaOTHER
165 Previous Clinical Trials
104,830 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am unable to give consent for myself.I am under 18 years old.I have difficulty making decisions due to cognitive issues.I do not fully understand English.
Research Study Groups:
This trial has the following groups:- Group 1: Group Coaching Program
- Group 2: Usual Treatment
Awards:
This trial has 0 awards, including: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.
Is enrollment for this research endeavor currently available?
"Per the details on clinicaltrials.gov, this trial is not accepting patients as of now. It debuted on July 1st 2023 and was last modified five days later on the 7th of that same month. Though applicants are uninvited at present, there are 66 other trials currently recruiting volunteers."
Answered by AI
What positive results are expected from this clinical investigation?
"The primary goal of this study, assessed at Baseline, 4 months and 9 months is to gauge the amount of alteration in patient participation. Secondary objectives include assessing change in self-compassion (as measured by Neff's Self Compassion Score Short Form), moral injury (through a Moral Injury Symptom Scale for Health Professions) and imposter syndrome symptoms (using Young's Imposter Syndrome Symptoms Scale)."
Answered by AI
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