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Study identifier: NCT05308537 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Randomized Controlled Trial of the Mindful Compassion Care Program in Reducing Psychological Distress Amongst Nurses During the COVID-19 Pandemic

Condition: Burnout · COVID-19  ·  Sponsor: Universita di Verona

PhaseNA
Planned participants33
Who can joinAll sexes, 25 Years to 65 Years
Healthy volunteersNo

About this study

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. 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 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). 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.

This description comes directly from the study's public registry record.

Talk to the study team

Antonio Lasalvia  ·  +39 045 8283901  ·  antonio.lasalvia@univr.it

Always discuss trial participation with your own doctor first.

Locations (1)

Università di VeronaVerona, Italia, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT05308537