- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07022613
- Original Trial
The Impact of Mindfulness-Based Stress Reduction on Mindfulness, Self-Compassion, and Perceived Stress Among Healthcare Professionals
Mindfulness is defined as a state of awareness in which an individual consciously pays attention to the present moment without judgment, reaction, or resistance, thereby promoting mental and psychological well-being.
Self-compassion refers to adopting a kind, understanding, and supportive attitude toward oneself. While mindfulness enables individuals to recognize sources of stress and develop strategies to cope with them, self-compassion encourages a gentle and caring approach toward oneself during this process. Research has shown that mindfulness practices enhance self-compassion and that these two constructs have a synergistic effect in reducing stress.
Work-related stress negatively affects both the professional functioning and overall health of individuals. Acknowledging the increasing prevalence of stress and stress-related illnesses, the International Labour Organization (ILO) officially included stress and stress-induced disorders in the list of occupational diseases in 2010. Compared to other professions, these stressors have a more profound physical and psychological impact on healthcare professionals. In this context, the concepts of mindfulness and self-compassion are critically important for enhancing the psychological resilience of healthcare professionals and improving their stress management skills.
This study is designed as a non-randomized, quasi-experimental pretest-posttest control group study to determine the effect of the Mindfulness-Based Stress Reduction (MBSR) program on the levels of mindfulness, self-compassion, and stress among healthcare professionals. Data collection tools will include a demographic information form, the Perceived Stress Scale (PSS), Mindful Attention Awareness Scale (MAAS), the A Scale to Mearsure Self-Compassion (SCS), and a Visual Analog Scale (VAS) for stress assessment. The research will be conducted with healthcare professionals working at Aksaray Training and Research Hospital, located in the central district of Aksaray, Turkey.
An 8-week Mindfulness-Based Stress Reduction (MBSR) program will be implemented for the intervention group. Data will be collected between May and December 2025. The results of the study will be analyzed using the Statistical Package for the Social Sciences (SPSS) version 25. In addition to standardized scales, the effectiveness of the MBSR program will also be evaluated using a biological stress marker-salivary cortisol.
The Mindfulness-Based Stress Reduction program implemented in this study is expected to contribute to the field of occupational health nursing. Furthermore, the program is anticipated to enhance healthcare professionals' abilities to consciously recognize their emotions, accept painful experiences with understanding rather than suppression, and transform negative thoughts and emotions into more constructive perspectives.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: LEYLA MUSLU
- Phone Number: +905072226632 +905369488003
- Email: leylamuslu@akdeniz.edu.tr
Study Contact Backup
- Name: BİRGÜL YAZAR
- Phone Number: +05072226632 +05072226632
- Email: birglyazar@gmail.com
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- The intervention group consisted of participants whose perceived stress levels were above the arithmetic mean, as measured by the Perceived Stress Scale
- Individuals who provided informed consent to participate in the study.
Exclusion Criteria:
- Individuals with communication impairments (e.g., hearing, vision, or speech difficulties)
- Individuals currently engaged in stress-reducing practices such as yoga or various forms of meditation
- Pregnant individuals
- Individuals receiving medical or psychosocial treatment
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: program designed specifically for healthcare professionals, the intervention group
In the first and last sessions, the Perceived Stress Scale (PSS), the Mindful Attention Awareness Scale (MAAS), the Self-Compassion Scale (SCS), and the Visual Analog Scale (VAS) will be administered, and saliva samples will be collected. In the remaining sessions, only the VAS-one of the stress measurement parameters-will be verbally administered. In this way, participants will be informed weekly about the progression of their stress levels. The program to be implemented in the study will consist of weekly sessions held over eight weeks. Each session will be conducted for groups of 10 participants, three consecutive days per week. |
The Mindfulness-Based Stress Reduction (MBSR) program is considered to offer healthcare professionals working under high levels of stress the opportunity to develop knowledge and skills in consciously recognizing their emotions, compassionately accepting painful feelings without suppression, and transforming negative thoughts and emotions into more constructive ones. In the first and last sessions, the Perceived Stress Scale (PSS), the Mindful Attention Awareness Scale (MAAS), the Self-Compassion Scale (SCS), and the Visual Analog Scale (VAS) will be administered, and saliva samples will be collected. In the remaining sessions, only the VAS-one of the stress measurement parameters-will be verbally administered. In this way, participants will be informed weekly about the progression of their stress levels. The program to be implemented in the study will consist of weekly sessions held over eight weeks. Each session will be conducted for groups of 10 participants, three consecutive days
Other Names:
|
|
No Intervention: control group
Participants will be interviewed twice: once at the beginning and once at the end of the intervention.During both the initial and final interviews, the Perceived Stress Scale (PSS), the Mindful Attention Awareness Scale (MAAS), the Self-Compassion Scale (SCS), and the Visual Analog Scale (VAS) will be administered, and saliva samples will be collected.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Perceived Stress Scale
Time Frame: Participants will complete the scale once in the first phase of the study, and again during the first and final (eighth) weeks of the second phase."
|
The Perceived Stress Scale (PSS) was developed by Cohen, Kamarck, and Mermelstein (1983).The PSS consists of 14 items and is designed to measure the degree to which situations in one's life are perceived as stressful. The internal consistency reliability of the scale, calculated based on item analysis, yielded a Cronbach's alpha coefficient of 0.84, and the test-retest correlation was found to be 0.87. Participants evaluate each item on a 5-point Likert-type scale ranging from "Never (0)" to "Very Often (4)." The scale comprises two subdimensions: perceived distress and perceived lack of control/self-efficacy. Items 1, 2, 3, 7, 11, 12, and 14 assess perceived distress, while items 4, 5, 6, 8, 9, 10, and 13 assess perceived lack of self-efficacy. Seven of the items, which are positively worded, are reverse scored. The total score on the PSS-14 ranges from 0 to 56, with higher scores indicating greater perceived stress. |
Participants will complete the scale once in the first phase of the study, and again during the first and final (eighth) weeks of the second phase."
|
|
Mindful Attention Awareness Scale
Time Frame: In the second phase of the study, the scale will be administered in both the first and the final (eighth) week.
|
The Mindful Attention Awareness Scale (MAAS) was developed by Brown and Ryan (2003), and its Turkish validity and reliability study was conducted by Özyeşil et al. (2011). The scale has a Cronbach's alpha internal consistency coefficient of .80 and a test-retest correlation of .86. The MAAS measures the general tendency to be aware of and attentive to present-moment experiences in daily life. It consists of 15 items and is rated on a 6-point Likert-type scale (almost always, very frequently, sometimes, rarely, very rarely, almost never). The scale has a unidimensional structure and yields a single total score. Higher scores on the scale indicate higher levels of mindfulness. |
In the second phase of the study, the scale will be administered in both the first and the final (eighth) week.
|
|
A Scale to Mearsure Self-Compassion
Time Frame: In the second phase of the study, the scale will be administered in both the first and the final (eighth) week.
|
The Self-Compassion Scale (SCS) was developed by Neff in 2003 and consists of 26 items. The scale measures six subdimensions: self-kindness, self-judgment, common humanity, isolation, mindfulness, and over-identification. It is rated on a 5-point Likert-type scale (1 = Almost Never, 2 = Rarely, 3 = Sometimes, 4 = Often, 5 = Almost Always). The overall reliability of the scale is high, with a Cronbach's alpha coefficient of .92. For the subscales, Cronbach's alpha values range between .75 and .81, indicating good internal consistency. |
In the second phase of the study, the scale will be administered in both the first and the final (eighth) week.
|
|
Visual Analog Scale
Time Frame: At the beginning of each session conducted with the intervention group in the second phase of the study, it is planned to use the Visual Analog Scale (VAS) to assess the participants' stress levels based on the previous week's evaluation.
|
At the beginning of each session conducted with the intervention group in the second phase of the study, it is planned to use the Visual Analog Scale (VAS) to assess the participants' stress levels based on the previous week's evaluation. The Visual Analog Scale (VAS) is a tool used to convert subjective, non-quantifiable values into numerical data. It consists of a 10-centimeter horizontal line marked with numbers from 1 to 10 at one-centimeter intervals. The VAS is a well-established and widely accepted assessment instrument in the global scientific literature.Within the context of this study, a score of 10 on the Visual Analog Scale (VAS) will represent the highest level of perceived stress ('very stressed'), whereas a score of 0 will represent the absence of stress ('not stressed at all |
At the beginning of each session conducted with the intervention group in the second phase of the study, it is planned to use the Visual Analog Scale (VAS) to assess the participants' stress levels based on the previous week's evaluation.
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- AkdenizU-SBF-BY-01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Healthcare Professionals
-
University of BeykentMaltepe UniversityNot yet recruitingSustainability | Climate Change | Healthcare Professionals
-
PXL University CollegeKorian; VitasNot yet recruitingHealthcare ProfessionalsBelgium
-
Istanbul University - Cerrahpasa (IUC)Hatay Mustafa Kemal Univercity; Turan ŞahmaranNot yet recruitingHealth Physics, Healthcare Professionals, Toolbox Trainings
-
Poitiers University HospitalNot yet recruitingNicotine Replacement Therapy | Healthcare Professionals | Tobacco Craving | Tabacco CessationFrance
-
gizem boztasCompletedArtificial Intelligence | Attitude | Perception | Healthcare Professionals | Technology Acceptance | Orthotics and Prosthetics | CompetencyTurkey (Türkiye)
-
Wake Forest University Health SciencesNot yet recruiting
-
Ahmed AA Wali, MDArabian Gulf University, BahrainRecruitingAttitude of Health Personnel | Healthcare Professionals | Awareness and Knowledge LevelEgypt
-
Najran UniversityCompletedHealthcare ProfessionalsSaudi Arabia
-
Novo Nordisk A/SCompletedDiabetes | Delivery Systems | Healthcare ProfessionalsDenmark
-
Novo Nordisk A/SCompletedDiabetes | Delivery Systems | Healthcare ProfessionalsUnited States
Clinical Trials on Mindfulness-Based Stress Reduction Program
-
Necmettin Erbakan UniversityCompletedDEPRESSION | ANXIETY | STRESS | HOPELESSNESS | MİNDFULNESSTurkey (Türkiye)
-
Ankara UniversityCompletedBreast Cancer | Nursing CariesTurkey
-
University of Maryland, BaltimoreCompletedChild Abuse SurvivorsUnited States
-
Agri Ibrahim Cecen UniversityAtaturk UniversityCompletedMindfulness Based Stress ReductionTurkey (Türkiye)
-
Ataturk UniversityCompleted
-
University of Thi-QarCompletedPsychological Stress | Academic StressIraq
-
Mersin UniversityNot yet recruiting
-
Ondokuz Mayıs UniversityCompleted
-
Halic UniversityCompletedMultiple Sclerosis | Mindfulness | Upper Motor Neuron LesionTurkey