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Effectiveness of a Mindful Compassion Care Program in reducing burnout and psychological distress amongst frontline hospital nurses during the COVID-19 pandemic: a study protocol for a randomized controlled trial.

Trials
January 1, 1970
Luca Bodini et al. (10 authors)
Clinical Trial ProtocolJournal ArticleHuman StudyClinical
Study Details

Study Goal

The researchers aimed to assess the feasibility, acceptability, and efficacy of a mindfulness and compassion-focused program in reducing burnout and emotional distress among frontline nurses during the COVID-19 pandemic.

Results Summary

The study will evaluate the impact of mindfulness and compassion interventions on emotional exhaustion, cynicism, professional efficacy, anxiety, depression, insomnia, stress perception, mindfulness, and self-criticism/reassurance among nurses. Results are pending as the study is a planned randomized controlled trial.

Population

Frontline nurses working during the COVID-19 pandemic at Verona University Hospital Trust in Italy.

Effective Dosage

Not specified

Duration

Not specified

Interactions

None mentioned

Extracted Claims (10)
InterventionDirectionEndpointPopulationDosageImpactClaim #
mindfulness and compassion interventions
decrease
burnout and emotional distress
healthcare professionals
-
effectiveness in reducing
#1
a mindfulness and compassion-focused programme
neutral
Emotional Exhaustion subscale of the Maslach Burnout Inventory General Survey (MBI-GS)
frontline nurses who had been working during the COVID-19 pandemic
-
will assess the feasibility, acceptability, and efficacy
#2
a mindfulness and compassion-focused programme
neutral
Cynicism and Professional Efficacy subscales of the MBI-GS
frontline nurses who had been working during the COVID-19 pandemic
-
will assess the feasibility, acceptability, and efficacy
#3
a mindfulness and compassion-focused programme
neutral
Patient Health Questionnaire (PHQ-9)
frontline nurses who had been working during the COVID-19 pandemic
-
will assess the feasibility, acceptability, and efficacy
#4
a mindfulness and compassion-focused programme
neutral
Generalized Anxiety Disorder (GAD-7)
frontline nurses who had been working during the COVID-19 pandemic
-
will assess the feasibility, acceptability, and efficacy
#5
a mindfulness and compassion-focused programme
neutral
Insomnia Severity Index (ISI)
frontline nurses who had been working during the COVID-19 pandemic
-
will assess the feasibility, acceptability, and efficacy
#6
a mindfulness and compassion-focused programme
neutral
Impact of Stressful Events (IES-R)
frontline nurses who had been working during the COVID-19 pandemic
-
will assess the feasibility, acceptability, and efficacy
#7
a mindfulness and compassion-focused programme
neutral
Perceived Stress Scale (PSS)
frontline nurses who had been working during the COVID-19 pandemic
-
will assess the feasibility, acceptability, and efficacy
#8
a mindfulness and compassion-focused programme
neutral
Five Facet Mindfulness Questionnaire (FFMQ)
frontline nurses who had been working during the COVID-19 pandemic
-
will assess the feasibility, acceptability, and efficacy
#9
a mindfulness and compassion-focused programme
neutral
Forms of Self-Criticising/attacking and Self-Reassuring Scale (FSCRS)
frontline nurses who had been working during the COVID-19 pandemic
-
will assess the feasibility, acceptability, and efficacy
#10
Abstract

BACKGROUND: Recent studies have shown that nurses have been more affected by the COVID-19 pandemic than any other group of hospital workers in terms of anxiety, depression, and burnout. Several clinical studies had previously demonstrated the effectiveness of mindfulness and compassion interventions in reducing burnout and emotional distress amongst healthcare professionals. METHODS AND ANALYSIS: A parallel-group randomized controlled trial will assess the feasibility, acceptability, and efficacy of a mindfulness and compassion-focused programme on frontline nurses who had been working during the COVID-19 pandemic. Seventy-two participants will be recruited from Verona University Hospital Trust (Veneto Region, north-east Italy) and will be divided equally into an intervention group and a control group. Primary outcome will be assessed using the Emotional Exhaustion subscale of the Maslach Burnout Inventory General Survey (MBI-GS). Secondary outcomes will be measured by the Cynicism and Professional Efficacy subscales of the MBI-GS, the Patient Health Questionnaire (PHQ-9), the Generalized Anxiety Disorder (GAD-7), the Insomnia Severity Index (ISI), the Impact of Stressful Events (IES-R), the Perceived Stress Scale (PSS), the Five Facet Mindfulness Questionnaire (FFMQ), and the Forms of Self-Criticising/attacking and Self-Reassuring Scale (FSCRS). DISCUSSION: The study aims to fill a gap in the literature and present a scientifically validated intervention for those healthcare professionals most exposed to the stressful conditions of working during the COVID-19 pandemic. TRIAL REGISTRATION: ClinicalTrials.gov; Identifier: NCT05308537.

Medical Subject Headings (MeSH)
Burnout, ProfessionalCOVID-19EmpathyHospitalsHumansMindfulnessPandemicsPsychological DistressRandomized Controlled Trials as Topic
Study Links
Quality Scores
SafetyNot Assessed
Efficacy75/10
Quality85/10
Citation Metrics
Total Citations4
Citations/Year1.3
Relative Citation Ratio0.98
NIH Percentile49.6%
Research Impact Scores
APT Score0.25
Weight Score1.61
Normalized Score0.67
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