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NCT Number: NCT07751926

Mindfulness-Based Stress Reduction for Workplace Stress Among Secondary School Teachers ( WORKPLACE STRESS )

This randomized controlled trial aims to evaluate the effectiveness of an eightweek Mindfulness-Based Stress Reduction (MBSR) program in reducing workplace stress among secondary school teachers from public and private schools in the Malakand Division, Khyber Pakhtunkhwa, Pakistan. Eligible teachers experiencing moderate to high workplace stress will be randomly assigned to either an MBSR intervention group or a wait-list control group. Stress levels will be assessed before and after the intervention using the Workplace Stress Scale (WSS) and the Perceived Stress Scale (PSS). The study also aims to compare stress levels between public and private school teachers and investigate gender differences in intervention outcomes. This description aligns with your synopsis objectives and design.

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Key information

Age range

18 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Riphah International University Malakand Campus

Swāt, KPK, 19000, Pakistan

About this study

Workplace stress is one of the most significant occupational health challenges among school teachers and negatively affects psychological well-being, teaching effectiveness, and educational quality. Teachers frequently encounter excessive workload, administrative demands, classroom management difficulties, and work-life imbalance, making them particularly vulnerable to chronic stress. Mindfulness-Based Stress Reduction (MBSR), developed by Jon Kabat-Zinn, is an evidence-based intervention designed to cultivate present-moment awareness and non-judgmental acceptance through mindfulness meditation, body scanning, mindful yoga, and other mindfulness practices. Numerous studies have demonstrated its effectiveness in reducing psychological stress and improving emotional well-being across diverse populations. This study will employ a two-arm parallel randomized controlled trial with pretest and posttest assessments. Eighty-six eligible secondary school teachers will be randomly allocated to either the experimental group receiving the standardized eight-week MBSR program or a wait-list control group receiving no intervention during the study period. The intervention consists of weekly 2.5-hour group sessions, a day-long retreat between Weeks 6 and 7, and daily home practice of 30-45 minutes. Outcome measures include workplace stress and perceived stress assessed before and immediately after the intervention. The study will also evaluate whether the effectiveness of MBSR differs by school sector (public versus private) and gender.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

(1) employed in a public or private school in Malakand Division, (2) had a WSS Total score of 24 or higher (moderate to high risk of workplace stress), (3) had a PSS-10 Total score of 20 or higher (moderate to high level of perceived stress), (4) were willing to provide written informed consent for the RCT and accept being randomly allocated to a group, and (5) speak Urdu or Pashto

Exclusion criteria

(1) participation at the time of recruitment in other structured psychological intervention, counselling and/or mindfulness program; (2) severe mental health diagnosis (psychosis, bipolar disorder, major depressive disorder with suicidal ideation and/or PTSD); (3) use of psychotropic medication at the time of recruitment; (4) absence from teaching for more than four consecutive weeks during the previous three months; (5) intention to leave the teaching post or change districts during the 8 week period of the program

Treatment and study plan

MBSR

Behavioral

Experimental Group Mindfulness-Based Stress Reduction (MBSR) Participants will receive the standardized eight-week MBSR program delivered in weekly 2.5-hour group sessions by trained instructors. The Experimental Group Mindfulness-Based Stress Reduction (MBSR) Participants will receive the standardized eight-week MBSR program delivered in weekly 2.5-hour group sessions by trained instructors. The intervention includes body scan meditation, sitting meditation, mindful yoga, breathing exercises, interpersonal mindfulness, a day-long mindfulness retreat, and daily home practice (30-45 minutes). Behavioral Intervention Mindfulness-Based Stress Reduction (MBSR)

________________________________________ Wait-list Control Group Participants assigned to the control group will continue their usual routine without receiving the intervention during the study period. They will be offered the MBSR program after completion of post-intervention assessments.

Primary outcomes

  1. Participants who engage in MBSR experience a statistically significant reduction in self-reported stress levels following the intervention.

    Time frame: Baeline to Week-8

    Participants receiving the eight-week Mindfulness-Based Stress Reduction (MBSR) intervention are expected to demonstrate a statistically significant decrease in workplace and perceived stress scores from baseline to post-intervention, as measured by validated stress assessment instruments.

Secondary outcomes

  1. Gender differences in the effectiveness of MBSR on stress reduction will be identified.

    Time frame: baseline to week-8

    The study will compare changes in stress scores between male and female teachers following the MBSR intervention to determine whether gender influences the effectiveness of the program in reducing workplace and perceived stress.

Sponsors and collaborators

Lead sponsor

Riphah International University

Other

Registry information

Official study title

Workplace Stress Among School Teachers: Minfulness Based Stress Reduction Intervention

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Aug 7, 2026
Registry last updated
Aug 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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