Kaltenborn Mobilization With and Without Proprioceptive Neuromuscular Facilitation Technique in Low Back Pain.

February 4, 2026 updated by: Riphah International University

Effects of Kaltenborn Mobilization With and Without Proprioceptive Neuromuscular Facilitation Technique on Pain, Range of Motion and Function in Patients With Chronic Non Specific Low Back Pain.

The study was conducted to determine the effects of Kaltenborn mobilization with and without proprioceptive neuromuscular facilitation technique on pain, range of motion and function in patients with chronic non-specific low back pain.

Study Overview

Study Type

Interventional

Enrollment (Actual)

50

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
        • General hospital lahore

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:

  • Age range of 25 to 45
  • Pain lasting for more than 3 months
  • Score between 2 to 7 in NPRS
  • Score of greater than 20 in ODI
  • Pain localized between the level below the ribs at the posterior side and above the level of buttocks.

Exclusion Criteria:

  • Any neoplasm involving back
  • Radiating pain
  • Metabolic disorders like osteoporosis
  • Pregnancy
  • Acute infection
  • Prior orthopedic surgeries
  • Acute trauma

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
Experimental: Kaltenborn Mobilization with Proprioceptive neuromuscular facilitation technique
Kaltenborn mobilization was applied to the lumbar spine area in the dorsal direction . Patient was positioned in flexion , side bending and rotation to the right and glide was applied in dorsal direction. Similar glide was given to patient in extension, side bending and rotation to the right. These techniques were performed for 3 days per week for 6 consecutive weeks.
PNF Hold Relax technique was performed on lumbar spine to increase the extensibility of the surrounding muscles after a maximal response. These techniques were performed for 3 days per week for 6 consecutive weeks.
Hotpack for 10 mins was applied with Tens at a burst mode with pulse width 200 microsec, frequency 100 Hz, burst frequency 2 Hz for 10 mins. Ultrasound was applied for 10 mins, stretching of calf, hamstrings and gluteals along with back strengthening.
Active Comparator: Kaltenborn mobilization
Kaltenborn mobilization was applied to the lumbar spine area in the dorsal direction . Patient was positioned in flexion , side bending and rotation to the right and glide was applied in dorsal direction. Similar glide was given to patient in extension, side bending and rotation to the right. These techniques were performed for 3 days per week for 6 consecutive weeks.
Hotpack for 10 mins was applied with Tens at a burst mode with pulse width 200 microsec, frequency 100 Hz, burst frequency 2 Hz for 10 mins. Ultrasound was applied for 10 mins, stretching of calf, hamstrings and gluteals along with back strengthening.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Numeric Pain Rating Scale
Time Frame: From enrollment to the end of treatment at 6 weeks.
Numeric Pain Rating scale is used to measure intensity of pain. It ranges from 0 to 10 where 0 represents no pain, 1-3 represents mild pain, 4-6 represents moderate pain and 7-10 shows severe pain.
From enrollment to the end of treatment at 6 weeks.
Oswestry Disability Index
Time Frame: From enrollment to the end of treatment at 6 weeks
Oswetry Disability index is a questionnaire consisting of 10 questions used to asses functional disability in patients with low back pain. In this scale, 0-20% = minimal disability, 21-40% = moderate disability, 41-60% = severe disability, 61-80% = crippled and 81-100% = bedbound.
From enrollment to the end of treatment at 6 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
ROM Lumbar spine (Flexion)
Time Frame: From enrollment to end of treatment at 6 weeks.
Changes in lumbar flexion range of motion was measured using goniometer at baseline and at the end of 6 weeks.
From enrollment to end of treatment at 6 weeks.
ROM of Lumbar Spine ( Extension)
Time Frame: From enrollment to the end of treatment at 6 weeks
Changes in lumbar extension range of motion was measured using goniometer at baseline to the end of treatment at 6 weeks.
From enrollment to the end of treatment at 6 weeks

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Shakil ur Rehman, Ph.D, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Thomas JS, Clark BC, Russ DW, France CR, Ploutz-Snyder R, Corcos DM; RELIEF Study Investigators. Effect of Spinal Manipulative and Mobilization Therapies in Young Adults With Mild to Moderate Chronic Low Back Pain: A Randomized Clinical Trial. JAMA Netw Open. 2020 Aug 3;3(8):e2012589. doi: 10.1001/jamanetworkopen.2020.12589.
  • Fouda KZ, Dewir IM, Abdelsalam MS. Effects of proprioceptive neuromuscular facilitation techniques in treating chronic nonspecific low back pain patients. Physiotherapy Quarterly. 2021;29(2):32-7.
  • Panjaitan LA, Hon WHC, Baait SN, Mawaddah N. Comparison between proprioceptive neuromuscular facilitation and mckenzie method in lumbar range of motion on non-specific low back pain. ACTIVE: Journal of Physical Education, Sport, Health and Recreation. 2020;9(1):63-71.
  • Mehyar F, Santos M, Wilson SE, Staggs VS, Sharma NK. Effect of grade III lumbar mobilization on back muscles in chronic low back pain: a randomized controlled trial. Journal of Allied Health. 2020;49(1):20-8.
  • Karkamandi F, Miri H, Letafatkar A, Haghighi M. Comparing the effects of motor control exercises and PNF exercises on postural control, strength, endurance, and proprioception in women with chronic nonspecific low back pain. Sport Sciences and Health Research. 2021;13(2):165-77.
  • Lizis P, Kobza W, Jaszczur-Nowicki J, Wisniewski D. Osteopathic Manual Treatment Compared to Kaltenborn-Evjenth Orthopedic Manual Therapy for Chronic Low Back Pain: A Randomized Study. Alternative Therapies in Health and Medicine. 2021:AT6593-AT.
  • Koutarapu S, Ghumare D. Proprioceptive neuromuscular facilitation exercises versus lumbar stabilization exercises for chronic low back pain patients: A randomized interventional study. The Indian Journal of Occupational Therapy. 2022;54(1):23-8.
  • Arcanjo FL, Martins JVP, Mote P, Leporace G, de Oliveira DA, de Sousa CS, et al. Proprioceptive neuromuscular facilitation training reduces pain and disability in individuals with chronic low back pain: A systematic review and meta-analysis. Complementary Therapies in Clinical Practice. 2022;46:101505.
  • Malik A, Ramsha M, Samad A. Outcomes of the butler neural mo-bilization technique and manual therapy for chronic low back pain in patients with lumbar radiculopathy: A cross-sectional comparative study. J Basic Clin Med Sci. 2022;1:3-11.
  • Kasimis K, Iakovidis P, Lytras D, Koutras G, Chatziprodromidou IP, Fetlis A, et al. Short-term effects of manual therapy plus capacitive and resistive electric transfer therapy in individuals with chronic non-specific low back pain: a randomized clinical trial study. Medicina. 2023;59(7):1275.
  • Shahzadi M, Tanveer S, Batool M, Sheikh SA, Faraz K, Fatima Z. Comparing Muscle Energy Technique and Kaltenborn-Evjenth Orthopaedic Manual Therapy: A Study on Effectiveness in Treating Chronic Low Back Pain. Journal of Health and Rehabilitation Research. 2023;3(2):1200-5.
  • Khalid R, Hasan S, Anis T, Riaz SW, Maroof A, Arshad A, et al. Comparative Effectiveness of Muscle Energy Technique (MET) With or Without Proprioceptive Neuromuscular Facilitation (PNF) Pattern in Lumbosacral Dysfunction: Comparative Effectiveness of Muscle Energy Technique (MET). THE THERAPIST (Journal of Therapies & Rehabilitation Sciences). 2024:51-5.
  • Deopa V, Kumar N, Thapliyal S, Sharma S. To Compare the Effect of PNF Stretching and Core Stabilizing Exercise Versus McKenzie Technique in Subjects with Low Back Pain.

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)

October 14, 2025

Primary Completion (Actual)

December 1, 2025

Study Completion (Actual)

December 5, 2025

Study Registration Dates

First Submitted

February 4, 2026

First Submitted That Met QC Criteria

February 4, 2026

First Posted (Actual)

February 11, 2026

Study Record Updates

Last Update Posted (Actual)

February 11, 2026

Last Update Submitted That Met QC Criteria

February 4, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Other Study ID Numbers

  • REC/RCR & AHS/24/0177

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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