Evaluating the Impact of Mindfulness Based Physical Therapy on Burnout Syndrome Among University Students.

March 27, 2026 updated by: Fansub Choudhary, University of Health Sciences Lahore

The goal of this clinical trial is to evaluate whether a mindfulness-based physical therapy intervention can reduce burnout syndrome and improve musculoskeletal pain and quality of life among undergraduate Allied Health Sciences students aged 18-30 years who are experiencing burnout symptoms, musculoskeletal pain, and reduced quality of life.

The main questions it aims to answer are:

  • Does a structured Mindfulness-Based Physical Therapy (MBPT) program reduce burnout symptoms compared to standard physical therapy alone?
  • Does MBPT improve musculoskeletal pain and quality of life compared to standard physical therapy alone?

Researchers will compare a Mindfulness-Based Physical Therapy intervention group to a control group receiving a standardized physical therapy program to determine whether the addition of mindfulness techniques results in greater improvements in burnout, pain, and quality of life.

Participants will:

  • Be randomly assigned to either the intervention or control group.
  • Attend supervised 60-minute sessions three times per week for six weeks (total of 18 sessions).
  • Receive a standardized baseline physical therapy program consisting of full-body active range of motion and general mobility exercises within pain-free limits.
  • If assigned to the intervention group, receive structured mindfulness meditation, breathing exercises, posture correction, stretching, progressive muscle relaxation, and group reflection during each session.
  • Complete 10-15 minutes of daily home mindfulness practice (intervention group only).
  • Complete validated questionnaires at baseline and immediately after the 6-week intervention.

Study Overview

Detailed Description

Burnout and musculoskeletal pain are common issues affecting university students, often resulting from prolonged stress, poor posture, and high academic demands. Mindfulness-based interventions have been shown to reduce stress, enhance resilience, and improve mental well-being. Physical therapy interventions, including exercise and rehabilitative techniques, target musculoskeletal pain and functional limitations. Combining mindfulness with physical therapy may provide a holistic, non-invasive approach to improving both mental and physical health in students.

This study evaluates the impact of a structured Mindfulness-Based Physical Therapy (MBPT) program on burnout syndrome, musculoskeletal pain, and quality of life among undergraduate Allied Health Sciences students aged 18-30 years. Participants will engage in a six-week program supervised by trained professionals, incorporating mindfulness exercises, stretching, posture correction, progressive muscle relaxation, and home practice. The control group will receive standard physical therapy, allowing the study to assess the additional benefits of the mindfulness component.

The findings of this trial may provide evidence for a low-cost, integrative intervention that universities can implement to support student health and wellness. If effective, MBPT could serve as a model for combined mind-body programs, helping to reduce burnout, improve functional capacity, and enhance quality of life, potentially contributing to better academic performance and long-term health outcomes. This research addresses a gap in the literature on combined mindfulness and physical therapy interventions for university populations and may inform the development of future student wellness initiatives.

Study Type

Interventional

Enrollment (Actual)

55

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Punjab Province
      • Lahore, Punjab Province, Pakistan, 54000
        • University of Health Sciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • University Students aged 18-30 years enrolled in an undergraduate Allied Health Sciences program.
  • Reporting burnout symptoms as assessed by the School Burnout Inventory (SBI).
  • Having musculoskeletal pain in at least one body region during the past 7 days or past 12 months (Assessed by the Nordic Musculoskeletal Questionnaire).
  • Having decline in the quality of life in at least one domain (physical, psychological, social, or environmental) (Assessed by the WHOQOL-BREF questionnaire).

Exclusion Criteria:

  • Current diagnosis of any psychiatric disorder or taking any medicine.
  • Current participation in another mindfulness, yoga or meditation intervention.
  • Musculoskeletal injury requiring surgical or medical care.
  • Student who has had major life upheavals recently, such as a family member loss.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Standard Physical Therapy (Control Group)
The control group will receive a standardized baseline physical therapy program consisting of supervised full-body active range of motion exercises and general mobility exercises (shoulder rolls, arm swings, and pelvic tilts) throughout the study duration. All exercises will be performed within pain-free limit
A supervised physical therapy program consisting of full-body active range of motion and general mobility exercises, including shoulder rolls, arm swings, and pelvic tilts, performed within pain-free limits.
Experimental: Mindfulness-Based Physical Therapy (MBPT)
The intervention group will undergo a standardized baseline physical therapy program followed by a structured Mindfulness-Based Physical Therapy (MBPT) program delivered over six consecutive weeks, three supervised 60-minute sessions per week, under the guidance of a registered physical therapist. Participants will also be instructed to perform daily home practice for 10-15 minutes.
Mindfulness Based Physical Therapy is a structured program combining supervised physical therapy exercises with mindfulness practices. The intervention includes guided mindfulness meditation (body scan and breath awareness), diaphragmatic and paced breathing exercises, posture correction and ergonomic education, gentle stretching of the neck, shoulders, and back, and progressive muscle relaxation. Sessions are delivered three times per week for six weeks under the supervision of a registered physiotherapist. Participants are also instructed to complete daily home practice incorporating mindfulness and stretching techniques.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Burnout Score
Time Frame: Baseline and Week 6 (post-intervention)
The primary outcome is the change in student burnout, measured with the School Burnout Inventory (SBI), which evaluates three domains: exhaustion related to study demands, cynicism toward academic work, and sense of inadequacy as a student. Higher scores indicate greater burnout. The School Burnout Inventory is a nine item scale, that utilizes a 6- point Likert scale, resulting in a minimum total score of 9 and a maximum total score of 54. The study will assess the mean subscale scores at baseline and Week 6. A decrease in scores indicates a reduction in burnout symptoms following the intervention.
Baseline and Week 6 (post-intervention)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Reduction in Musculoskeletal Pain
Time Frame: Baseline and Week 6 (post-intervention)
Musculoskeletal pain will be evaluated using the Nordic Musculoskeletal Questionnaire (NMQ), which assesses the presence and location of musculoskeletal pain or discomfort over the past 7 days and past 12 months. It is primarily a categorical screening tool reporting prevalence as "Yes" or "No" for symptoms in nine anatomical regions. Pain levels will be recorded at baseline and Week 6. A reduction in reported symptoms will indicate improvement due to the intervention.
Baseline and Week 6 (post-intervention)
Improvement in Quality of Life
Time Frame: Baseline and Week 6 (post-intervention)
Quality of life will be assessed using the World Health Organization Quality of Life Instrument (WHOQOL-BREF), which measures physical, psychological, social, and environmental domains. It is a 26 item scale in which raw scores are typically transformed into a linear scale ranging from 0 (minimum value) to 100 (maximum value). Higher scores indicate better quality of life. Scores will be collected at baseline and Week 6. An increase in domain scores will indicate improvement following the intervention.
Baseline and Week 6 (post-intervention)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Fansub Choudhary, University of Health Sciences, Lahore, Pakistan

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 3, 2026

Primary Completion (Estimated)

March 30, 2026

Study Completion (Estimated)

April 20, 2026

Study Registration Dates

First Submitted

March 2, 2026

First Submitted That Met QC Criteria

March 2, 2026

First Posted (Actual)

March 6, 2026

Study Record Updates

Last Update Posted (Actual)

April 2, 2026

Last Update Submitted That Met QC Criteria

March 27, 2026

Last Verified

March 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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.

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