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single for Compassion Fatigue (CSRS Trial)
N/A
Waitlist Available
Led By Colleen Klein, PhD, MS, RN
Research Sponsored by OSF Healthcare System
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 change from baseline compassion satisfaction subscale measure at 1 and 6 months assessed by compassion satisfaction subscale of proqol 5 [ time frame: data collected before the program starts and one month after the end of the program and six months
Awards & highlights
CSRS Trial Summary
This trial will help health workers learn how to take care of themselves to prevent compassion fatigue and improve resilience.
Eligible Conditions
- Compassion Fatigue
- Secondary Traumatic Stress
- Resilience
CSRS Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change from baseline in resilience measure at 1 month and 6 months assessed by brs scale [ time frame: data collected before the program starts and one month after the end of the program and six months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline in resilience measure at 1 month and 6 months assessed by brs scale [ time frame: data collected before the program starts and one month after the end of the program and six months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Brief Resilience Scale
Professional Quality of Life Scale (ProQOL) Version 5
CSRS Trial Design
1Treatment groups
Experimental Treatment
Group I: singleExperimental Treatment1 Intervention
Educational intervention.
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Who is running the clinical trial?
OSF Healthcare SystemLead Sponsor
29 Previous Clinical Trials
33,665 Total Patients Enrolled
Colleen Klein, PhD, MS, RNPrincipal InvestigatorOSF Healthcare System
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You are currently enrolled in, or plan to enroll in, another program that teaches mindfulness-based stress reduction during the study period.
Research Study Groups:
This trial has the following groups:- Group 1: single
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 participants being accepted in this experiment?
"As indicated on clinicaltrials.gov, this particular medical study is not currently looking for participants; the trial was first published in April 2021 and last updated in August 2022. However, there are 226 other trials that remain open to new patients at this time."
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