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Clinical Trials/NCT06804720
NCT06804720CompletedNot Applicable

Self-Compassion As a Well-Being Strategy Against Occupational Burnout in Dentistry: a Controlled Clinical Trial

Cukurova University1 site in 1 country49 target enrollmentStarted: March 1, 2024Last updated:
Conditions
Interventions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
49
Locations
1
Primary Endpoint
Self-Compassion Scale

Study Overview

Brief Summary

Although studies have highlighted the relationship between stress-related psychopathological symptoms and changes in biochemical parameters, no study in dentistry has concurrently evaluated the association of stress and relaxation with biochemical markers and psychological parameters. Moreover, the impact of mindfulness-based self-compassion training programs on these variables has yet to be explored within this context. To enhance the well-being of dentists, an evaluation of a test group participating in an 8-week Mindfulness-Based Compassionate Living (MBCL) program was conducted. This assessment included daily cortisol curves, as well as salivary IL-6, IL-1β, and oxytocin levels. Additionally, empathy, burnout, self-compassion, depression, and mindfulness levels were measured before and after the training. In this study, the main hypothesis was that, compared to the control group, the test group would exhibit lower IL-1β, IL-6, and cortisol levels, along with higher oxytocin levels. Furthermore, as the secondary hypotheses was that the test group would demonstrate increased empathy, self-compassion, and mindfulness levels, accompanied by reductions in depression and burnout scores.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Health Services Research
Masking
Single (Outcomes Assessor)

Eligibility Criteria

Ages
24 Years to 35 Years (Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • •dentists in their final year of specialty training at the Faculty of Dentistry,
  • •systemicaly healthy

Exclusion Criteria

  • •individuals who received a diagnosis of mood disorders based on DSM-5 criteria following a standard diagnostic assessment conducted by psychiatrists from the Department of Psychiatry

Arms & Interventions

Test group (Self Compassion Training group)

Experimental

Intervention: Mindfulness based Self compassion (Behavioral)

Control group (No training)

No Intervention

Outcomes

Primary Outcomes

Self-Compassion Scale

Time Frame: Baseline and after 8 weeks

The 6 subscales that comprise the 26-item self-compassion scale are self-kindness, self-judgment , common humanity , isolation , mindfulness and over-identification Participants indicate their responses to each item using a 5-point scale ranging from 1 (Almost Never) to 5 (Almost Always). Higher score indicates greater self-compassion.

Secondary Outcomes

  • Saliva Cortisol(Baseline and after 8 weeks)
  • Saliva IL 6(Baseline and after 8 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Cenk Haytac

Professor

Cukurova University

Study Sites (1)

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