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Interprofessional Group Intervention to Enhance Compassion Satisfaction and Resilience (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
No Placebo-Only Group

Summary

This trial evaluates an educational program that helps healthcare workers learn self-awareness and self-care to prevent compassion fatigue. It targets healthcare professionals who face high stress levels. The program works by teaching them how to manage stress and take care of themselves.

Eligible Conditions
  • Compassion Fatigue
  • Resilience

Timeline

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
This trial's timeline: 3 weeks for screening, Varies for treatment, and 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 for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Brief Resilience Scale
Professional Quality of Life Scale (ProQOL) Version 5

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

1Treatment groups
Experimental Treatment
Group I: singleExperimental Treatment1 Intervention
Educational intervention.

Find a Location

Who is running the clinical trial?

OSF Healthcare SystemLead Sponsor
30 Previous Clinical Trials
33,745 Total Patients Enrolled
Colleen Klein, PhD, MS, RNPrincipal InvestigatorOSF Healthcare System

Media Library

Educational Intervention Clinical Trial Eligibility Overview. Trial Name: NCT04888000 — N/A
Compassion Fatigue Research Study Groups: single
Compassion Fatigue Clinical Trial 2023: Educational Intervention Highlights & Side Effects. Trial Name: NCT04888000 — N/A
Educational Intervention 2023 Treatment Timeline for Medical Study. Trial Name: NCT04888000 — N/A
~2 spots leftby Dec 2025
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