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Interprofessional Group Intervention to Enhance Compassion Satisfaction and Resilience

An Exploratory Study Examining Use of the Oxygen for Caregivers® Program

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04888000
Acronym
CSRS
Enrollment
11
Registered
2021-05-17
Start date
2021-04-29
Completion date
2023-11-01
Last updated
2023-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Compassion Fatigue, Resilience

Keywords

Compassion Fatigue, Resilience

Brief summary

The purpose of this study is to evaluate an educational professional development program designed to assist health care professionals in developing self-awareness and self-care choices as a means to avoid compassion fatigue and improve resilience.

Detailed description

Professional caregivers are at risk of compassion fatigue due to the nature of their work and repeated exposure over time to work-related stressors. Symptoms of compassion fatigue may include decreased concentration/productivity, increased sick days, and high turnover rates which directly effect patient satisfaction and safety. Lack of data that supports this use of program, though anecdotally, it has been endorsed and benefits from its use are described. Quality of patient care, workforce engagement, and financial effects from turnover of staff are viewed as negative impacts from compassion fatigue. Our study seeks to extend the body of knowledge with regard to use of a particular resilience program that has shown some promise in a small pilot study.

Interventions

OTHEREducational Intervention

Professional development program provided to small groups of health care professionals in three different sessions over a period of one month with additional independent individual work to be completed between sessions.

Sponsors

OSF Healthcare System
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Single Group Assignment

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* employment within inpatient or outpatient setting in non-profit healthcare system as a healthcare professional * Professional direct caregivers (nurses, physicians, advanced practice providers, social workers, counselors, chaplains, respiratory therapists, pharmacists

Exclusion criteria

* actively participating in or plans to participate in any other formalized mindfulness-based stress reduction program during the time period of the study

Design outcomes

Primary

MeasureTime frameDescription
Professional Quality of Life Scale (ProQOL) Version 5Change from baseline compassion fatigue subscale measure at 1 and 6 months assessed by compassion fatigue subscale of ProQOL 5 [ Time Frame: Data collected before the program starts and one month after the end of the program and six monthsProfessional Quality of Life Scale (ProQOL) Version 5 Compassion Fatigue Subscale
Brief Resilience ScaleChange 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 monthsResilience will be measured using the Brief Resilience Scale (BRS) a 6-item scale developed by Smith et al.(2008).

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026