CClinicalTrials.gg
Active, not recruitingNCT07456527Updated Apr 2, 2026

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

An interventional study of Standard Physical Therapy and Mindfulness Based Physical Therapy in Burnout Syndrome, sponsored by University of Health Sciences Lahore. Active, not recruiting at 1 site in Pakistan. Open to participants aged 18 Years to 30 Years. Per ClinicalTrials.gov, last updated 2026-04-02.

Sponsored by University of Health Sciences Lahore · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Mar 2026, 6 months ago, but the record still lists the study as active, not recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
55
Allocation
Randomized
Ages
18 Years to 30 Years
Sex
All
01

Study summary

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.
Read the 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.

02

Conditions studied

  • Burnout Syndrome

Keywords

  • Mindfulness Based Physical Therapy
  • MBPT
  • Mindfulness
  • Mindfulness interventions
  • Physical Therapy
  • Burnout
  • Burnout Syndrome
  • Musculoskeletal pain
  • Quality of life
  • University students
  • Randomized Controlled Trial
03

In context

Burnout, Psychological

442 studies on the registry are indexed under Burnout, Psychological; 106 are open to participants now.

This study's enrollment of 55 is below the median of 80 across 319 interventional studies indexed under Burnout, Psychological.

Browse Burnout, Psychological studies →

Lead sponsor

University of Health Sciences Lahore is the lead sponsor of 77 studies on the registry; 49 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 30 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
55 participants (actual)

Study arms

  • 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

    Behavioral: Standard Physical Therapy

  • 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.

    Behavioral: Mindfulness Based Physical Therapy

Interventions

  • BehavioralStandard Physical Therapy

    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.

  • BehavioralMindfulness Based Physical Therapy

    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.

06

What researchers measure

Primary outcomes

  1. Change in Burnout Score

    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.

    Time frame: Baseline and Week 6 (post-intervention)

Secondary outcomes

  1. Reduction in Musculoskeletal Pain

    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.

    Time frame: Baseline and Week 6 (post-intervention)

  2. Improvement in Quality of Life

    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.

    Time frame: Baseline and Week 6 (post-intervention)

07

Study locations

1 site
  • University of Health Sciences
    Lahore, Punjab Province 54000, Pakistan
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 2, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07456527
Lead sponsor
University of Health Sciences Lahore
Responsible party
Fansub Choudhary (Principal Investigator, University of Health Sciences Lahore) — Principal investigator
First posted
Mar 6, 2026
Start date
Jan 3, 2026
Primary completion
Mar 30, 2026 (estimated)
Completion
Apr 20, 2026 (estimated)
Last update
Apr 2, 2026

Study contacts

Fansub Choudhary
principal investigator · University of Health Sciences, Lahore, Pakistan

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion