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Controlled clinical trial comparing the effectiveness of a mindfulness and self-compassion 4-session programme versus an 8-session programme to reduce work stress and burnout in family and community medicine physicians and nurses: MINDUUDD study protocol.

BMC family practice
January 1, 1970
Luis-Angel Pérula-de Torres et al. (16 authors)
Clinical Trial ProtocolJournal ArticleResearch Support, Non-U.S. Gov'tHuman StudyClinical
Study Details

Study Goal

The researchers aimed to evaluate the effectiveness of a 4-session mindfulness and self-compassion program versus an 8-session standard program in reducing work stress and burnout among Family and Community Medicine and Nursing tutors and residents.

Results Summary

The study compared two mindfulness intervention durations (4 vs. 8 sessions) and a control group, measuring outcomes like stress, burnout, empathy, and anxiety-depression. Results were pending at the time of the abstract, but the study hypothesized that the abbreviated program could be as effective as the standard one, making it more feasible for implementation.

Population

Family and Community Medicine and Nursing tutors and residents.

Effective Dosage

EG8: 8 weekly sessions of 2.5 hours each with 30 minutes/day home practice; EG4: 4 sessions of 2.5 hours each with 15 minutes/day home practice.

Duration

8 weeks for EG8, 4 weeks for EG4.

Interactions

None mentioned.

Extracted Claims (2)
InterventionDirectionEndpointPopulationDosageImpactClaim #
mindfulness and self-compassion 4-session programme
decrease
work stress and burnout
Family and Community Medicine and Nursing tutors and residents
-
reduce
#1
mindfulness and self-compassion 8-session programme
decrease
work stress and burnout
Family and Community Medicine and Nursing tutors and residents
-
reduce
#2
Abstract

BACKGROUND: Health personnel are susceptible to high levels of work stress and burnout due to the psychological and emotional demands of their work, as well as to other aspects related to the organisation of that work. This paper describes the rationale and design of the MINDUUDD study, the aim of which is to evaluate the effectiveness of a mindfulness and self-compassion 4-session programme versus the standard 8-session programme to reduce work stress and burnout in Family and Community Medicine and Nursing tutors and residents. METHODS: The MINDUDD study is a multicentre cluster randomised controlled trial with three parallel arms. Six Teaching Units will be randomised to one of the three study groups: 1) Experimental Group-8 (EG8); 2) Experimental Group-4 (EG4) Control group (CG). At least 132 subjects will participate (66 tutors/66 residents), 44 in the EG8, 44 in the EG4, and 44 in the CG. Interventions will be based on the Mindfulness-Based Stress Reduction (MBSR) program, including some self-compassion practices of the Mindful Self-Compassion (MSC) programme. The EG8 intervention will be implemented during 8 weekly face-to-face sessions of 2.5 h each, while the EG4 intervention will consist of 4 sessions of 2.5 h each. The participants will have to practice at home for 30 min/day in the EG8 and 15 min/day in the EG4. The Five Facet Mindfulness Questionnaire (FFMQ), Self-Compassion Scale (SCS), Perceived Stress Questionnaire (PSQ), Maslach Burnout Inventory (MBI), Jefferson Scale of Physician Empathy (JSPE), and Goldberg Anxiety-Depression Scale (GADS) will be administered. Measurements will be taken at baseline, at the end of the programs, and at three months after completion. The effect of the interventions will be evaluated by bivariate and multivariate analyses (Multiple Linear Regression). DISCUSSION: If the abbreviated mindfulness programme is at least as effective as the standard program, its incorporation into the curriculum and training plans will be easier and more appropriate. It will also be more easily applied and accepted by primary care professionals because of the reduced resources and means required for its implementation, and it may also extend beyond care settings to academic and teaching environments as well. TRIAL REGISTRATION: The study has been registered at ClinicalTrials.gov ( NCT03629457 ; date of registration: 13.08.2018).

Medical Subject Headings (MeSH)
HumansBurnout, ProfessionalCommunity MedicineEmpathyEquivalence Trials as TopicMindfulnessNursesOccupational StressPhysicians, FamilySpainMulticenter Studies as TopicRandomized Controlled Trials as Topic
Study Links
Quality Scores
SafetyNot Assessed
Efficacy75/10
Quality85/10
Citation Metrics
Total Citations26
Citations/Year4.3
Relative Citation Ratio2.80
NIH Percentile83.5%
Research Impact Scores
APT Score0.75
Weight Score1.84
Normalized Score0.67
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