Clinical trial Recruiting at 1 site Interventional Ages 18 to 65

Evaluating Feldenkrais and Otago exercises for low back pain relief

Official title: Effects of Feldenkrais and Otago Exercise Protocols for Mechanical Low Back Pain

Run by Riphah International University · NCT06985849 · Data updated 2026-11-12

This study is testing whether the Feldenkrais Method or Otago exercises can help adults aged 18 to 65 with chronic low back pain feel better and improve their daily activities.

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment36 (estimated)
SponsorRiphah International University
Academic / other
Locations1 site (Lahore)
StatusRecruiting
StartedDecember 15, 2024
Main results expectedMay 15, 2025
Study endsJune 15, 2025
Registry record updatedMay 22, 2025
Trial IDNCT06985849 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18 to 65 with chronic low back pain lasting at least three months and moderate pain and disability levels.

Probably not a fit

Patients with severe low back pain, significant balance impairment, or specific health conditions like cardiovascular disease and diabetes may not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This study investigates the effectiveness of the Feldenkrais Method and the Otago Exercise Programme in alleviating chronic low back pain and improving functional abilities in adults aged 18 to 65. Participants will be randomly assigned to one of the two intervention protocols, with data collected to assess pain levels, disability, and balance. The study aims to provide evidence for these interdisciplinary approaches in managing mechanical low back pain and reducing fall risks among older adults. Conducted at Farooq Hospital and Boston Physiotherapy and Wellness Clinic, it seeks to enhance understanding of non-pharmacological treatments for this common condition.

Why it matters

Potential benefit: If successful, this study could provide effective non-invasive treatment options for individuals suffering from chronic low back pain.

How similar studies have gone: Previous studies have shown promise in using similar non-invasive approaches for managing low back pain, suggesting potential for success in this trial.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* • Age group 18 to 65 year (3)

  * Both gender male and female
  * LBP (duration ≥ 3 months) (3)
  * NPRS score ≥ 4/10 (indicating moderate pain)
  * ODI: Score ≥ 20/100 (indicating moderate disability)
  * BBS: Score ≤ 45/56 (indicating balance impairment)
  * BC Scale score: ≤ 60/100 (indicating moderate to low balance confidence)
  * Ability to walk independently
  * No severe cognitive impairment
  * Patient willing to perform in the study

Exclusion Criteria:

* • Recurrent spinal surgery(3)

  * Malignancy
  * Spine Infection
  * Spinal fracture
  * Congenital disturbance
  * Severe LBP (NPRS ≥ 9/10)
  * Significant balance impairment (BBS ≤ 20/56)
  * Severe disability (ODI ≥ 60/100)
  * ABC Scale score: ≥ 80/100 (indicating high balance confidence)
  * Older individuals with specific health conditions, such as cardiovascular disease and diabetes

Where it's running

  • Farooq Hospital
    Lahore, Pakistan
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.