ClinicalTrials.gg
CompletedNCT07751926Updated Sep 1, 2026

Workplace Stress Among School Teachers: Minfulness Based Stress Reduction Intervention

An interventional study of MBSR in MBSR and Workplace Stress, sponsored by Riphah International University. Completed at 1 site in Pakistan. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-01.

Sponsored by Riphah International University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 1 year after the study started (first participant enrolled Jul 2025, registered Aug 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
86
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • MBSR
  • Workplace Stress

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03

In context

Occupational Stress

237 studies on the registry are indexed under Occupational Stress; 64 are open to participants now.

This study's enrollment of 86 is close to the median of 86 across 169 interventional studies indexed under Occupational Stress.

Browse Occupational Stress studies →

Lead sponsor

Riphah International University is the lead sponsor of 2,193 studies on the registry; 650 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Secondary school teachers employed in public or private schools in District Swat, Pakistan.
  • Currently employed as a full-time teacher with at least one year of teaching experience.
  • Reporting moderate to high workplace stress, as determined by the Workplace Stress Scale (WSS) during screening.
  • Able to read and understand Urdu or English.
  • Willing to participate in the 8-week Mindfulness-Based Stress Reduction (MBSR) program.
  • Able to attend weekly intervention sessions and complete home practice assignments.
  • Willing to provide written .

Exclusion criteria

Exclusion Criteria:

  • Current diagnosis of a severe psychiatric disorder (e.g., psychotic disorders, bipolar disorder, or severe major depressive disorder) that may interfere with participation.
  • Current participation in another psychological or stress-management intervention.
  • Regular mindfulness, meditation, or yoga practice (defined as practicing at least once per week during the previous six months).
  • Cognitive impairment or neurological disorder that would prevent completion of study assessments or participation in the intervention.
  • Planned extended leave, retirement, or transfer from the school during the study period.
  • Inability or unwillingness to attend the intervention sessions or complete the study assessments.
  • Declines or withdraws at any stage of the study.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
86 participants (actual)

Study arms

  • Experimental
    Experimental A

    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)

    Behavioral: MBSR

  • No intervention
    Control B

    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.

Interventions

  • BehavioralMBSR

    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.

06

What researchers measure

Primary outcomes

  1. Change from Baseline in Workplace Stress Scale Scores at 8 Weeks

    Workplace stress will be measured using the Workplace Stress Scale (WSS), an 8-item self-report questionnaire that assesses occupational stress experienced in the workplace. Each item is rated on a 5-point Likert scale ranging from 1 (Never) to 5 (Very Often). Total scores range from 8 to 40, with higher scores indicating greater workplace stress. The primary outcome will be the change in total WSS score from baseline (Week 0) to post-intervention (Week 8).

    Time frame: Baseline (Week 0) and Post-intervention (Week 8)

Secondary outcomes

  1. Change from Baseline in Perceived Stress Scale Scores at 8 Weeks

    Perceived stress will be measured using the Perceived Stress Scale (PSS-10), a 10-item self-report questionnaire assessing the extent to which individuals perceive situations in their lives as stressful during the previous month. Items are rated on a 5-point Likert scale from 0 (Never) to 4 (Very Often). Total scores range from 0 to 40, with higher scores indicating greater perceived stress. The secondary outcome will be the change in total PSS-10 score from baseline (Week 0) to post-intervention (Week 8).

    Time frame: Baseline (Week 0) and Post-intervention (Week 8)

Other outcomes

  1. Change from Basaseline in Mean Workplace Stress Scale Scores Between Experimental and Control Groups at 8 Weeks

    The mean change in Workplace Stress Scale (WSS) total scores from baseline to Week 8 will be compared between participants receiving the Mindfulness-Based Stress Reduction (MBSR) intervention and those in the control group. Total WSS scores range from 8 to 40, with higher scores indicating greater workplace stress.

    Time frame: after 8 weeks intervention

07

Study locations

1 site
  • Riphah International University Malakand Campus
    Swāt, KPK 19000, Pakistan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Jul 2025 to primary completion in Apr 2026, 9 months.

Of 127 non-industry interventional studies with no phase under Occupational Stress, half reached primary completion within 10 months of starting (the median), counting those still running; a quarter within 5 and three quarters within 28. This study's 9 months is close to that.

Counting every sponsor, half of 135 studies reached it within 10 months; a quarter within 5 and three quarters within 27.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 4, 2026
First posted
Aug 7, 2026
StartActual
Jul 10, 2025
Primary completionActual
Apr 10, 2026
CompletionActual
Jul 10, 2026
Last update
Sep 1, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 1, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07751926
Responsible party
Sponsor
First posted
Aug 7, 2026
Start date
Jul 10, 2025
Primary completion
Apr 10, 2026
Completion
Jul 10, 2026
Last update
Sep 1, 2026

Study contacts

Mazhar Ali
principal investigator · Riphah International University Malakand Campus

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Aug 2026. You cannot join it, but the record below documents what was studied.

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