Actively Recruiting

Phase Not Applicable
Age: 25Years - 60Years
All Genders
ID07280806

Biopsychosocial Model-based Care Versus Routine Physical Therapy in Chronic Back Pain

Led by Lahore University of Biological and Applied Sciences · Updated on 2026-03-09

80

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Chronic low back pain (CLBP) is a persistent condition influenced by physical, psychological, and social factors. This trial compares biopsychosocial (BPS) model-based care with routine physical therapy to evaluate their effects on pain, disability, psychosocial outcomes, and inflammation in adults aged 25 to 60 years with CLBP lasting 12 weeks or more. The study aims to provide evidence supporting a holistic approach to managing chronic low back pain. Participants are randomly assigned to either the Routine Physical Therapy group or the BPS Model-Based Care group. Both groups receive baseline treatments including hot packs and TENS, stretching, and strengthening exercises administered three times weekly over four weeks. The BPS group additionally receives manual therapy, neural mobilization, cognitive behavioral therapy, pain education, guided imagery, and group exercise therapy to address psychological and social factors. Participants will attend supervised therapy sessions lasting about 45 minutes each, three times a week for four weeks. Outcomes such as pain self-efficacy, functional disability, inflammatory markers, and perceived social support will be measured at baseline, after the intervention, and at follow-up. The study uses questionnaires and biochemical assessments to evaluate physical, psychological, and social dimensions of recovery in chronic low back pain.

CONDITIONS

Brief Title

Biopsychosocial Model-based Care Versus Routine Physical Therapy in Chronic Back Pain

Who Can Participate

Age: 25Years - 60Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with non-specific chronic low back pain lasting more than 12 weeks
  • Pain intensity score of 3 or higher on the Visual Analog Scale
  • Able to read and understand study instructions and questionnaires
  • Not currently undergoing structured physiotherapy or psychological treatment for low back pain
  • Aged between 25 and 60 years
Not Eligible

You will not qualify if you...

  • History of specific spinal pathology such as fracture, tumor, infection, or inflammatory disease
  • Presence of neurological deficits like radiculopathy or cauda equina syndrome
  • Previous lumbar spine surgery
  • Current major psychiatric illness interfering with participation
  • Pregnancy or within 6 months postpartum
  • Ongoing treatment with systemic corticosteroids or medications affecting musculoskeletal health
  • Participation in another clinical trial within the past 3 months
  • Any other medical condition deemed unsafe for participation by the investigator

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 4 weeks

Participants receive physical therapy sessions three times per week for 4 weeks. The Biopsychosocial group receives a multimodal program including physical, psychological, and social components, while the Routine Physical Therapy group receives standard physical therapy focused on pain relief and muscle strengthening.

3 visits per week for 4 weeks

Follow-up

Duration - 4 weeks

Participants are assessed for pain intensity, functional disability, and other outcomes 4 weeks after completing treatment to evaluate lasting effects.

1 visit (in-person) at 8 weeks post-baseline

Trial Site Locations

Total: 1 location

1

University of Lahore

Lahore, Punjab Province, Pakistan, 05450

Actively Recruiting

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Research Team

M

Muhammad Tariq, BSPT, tDPT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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