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McGill Versus Sahrmann's Exercises for Chronic Non-Specific Low Back Pain

Effects of McGill Versus Sahrmann's Protocol on Pain, Range of Motion and Disability in Chronic Non- Specific Low Back Pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07724704
Enrollment
40
Registered
2026-07-24
Start date
2026-07-16
Completion date
2026-09-16
Last updated
2026-07-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Non-specific Low Back Pain

Keywords

Chronic Non-Specific Low Back Pain, McGill Stabilization Exercise Protocol, Sahrmann Exercise Protocol, Pain Intensity, Lumbar Range of Motion, Functional Disability, Core Stabilization Exercises, Numeric Pain Rating Scale (NPRS), Oswestry Disability Index (ODI), Bubble Inclinometer

Brief summary

The goal of this clinical trial is to compare the effects of McGill stabilization exercises and Sahrmann's movement-based exercise protocol in adults with chronic non-specific low back pain. The study aims to determine which exercise program is more effective in reducing pain, improving lumbar range of motion, and decreasing functional disability. The main questions it aims to answer are: Do McGill stabilization exercises reduce pain, improve lumbar range of motion, and decrease disability in individuals with chronic non-specific low back pain? Are McGill stabilization exercises more effective than Sahrmann's movement-based exercise protocol in improving pain, lumbar range of motion, and functional disability? Researchers will compare the McGill stabilization exercise group with the Sahrmann exercise group to determine which intervention provides greater improvements in clinical outcomes. Participants will: Be randomly assigned to either the McGill stabilization exercise group or the Sahrmann exercise group. Receive baseline physiotherapy, including hot pack application, Transcutaneous Electrical Nerve Stimulation (TENS), lumbar isometric exercises, pelvic tilts, knee-to-chest exercises, and manual therapy. Attend supervised treatment sessions 2-3 times per week for 6 weeks. Complete outcome assessments before and after treatment using the Numeric Pain Rating Scale (NPRS) for pain, the Oswestry Disability Index (ODI) for disability, and a bubble inclinometer to measure lumbar range of motion. This study will provide evidence on the comparative effectiveness of two commonly used physiotherapy exercise protocols and help identify the most effective rehabilitation approach for managing chronic non-specific low back pain.

Detailed description

Chronic non-specific low back pain (CNSLBP) is one of the leading causes of disability worldwide and is associated with persistent pain, reduced spinal mobility, impaired motor control, and limitations in daily activities. Unlike specific low back pain, CNSLBP has no identifiable pathological cause, making rehabilitation through exercise therapy the primary treatment approach. Current clinical guidelines recommend exercise-based interventions to improve pain, function, and quality of life; however, there is no consensus regarding the most effective exercise protocol for individuals with chronic non-specific low back pain. Among the commonly prescribed physiotherapy interventions are the McGill stabilization exercise program and Sahrmann's movement-based exercise protocol. The McGill approach focuses on enhancing spinal stability by improving core muscle endurance and minimizing excessive spinal loading through spine-sparing stabilization exercises. In contrast, Sahrmann's protocol emphasizes correction of movement impairments, restoration of normal lumbopelvic movement patterns, and activation of deep stabilizing muscles to improve motor control and functional movement. Although both rehabilitation approaches have demonstrated beneficial effects when studied individually, direct comparative evidence regarding their effectiveness in improving pain, lumbar range of motion, and functional disability remains limited. Existing studies have primarily evaluated each intervention separately or compared them with conventional physiotherapy rather than with each other. Consequently, clinicians have limited evidence to guide the selection of the most appropriate exercise protocol for patients with chronic non-specific low back pain. This randomized controlled trial is designed to compare the clinical effectiveness of McGill stabilization exercises and Sahrmann's movement-based exercise protocol in adults with chronic non-specific low back pain. Clinical outcomes will be evaluated using validated measures of pain intensity, lumbar range of motion, and functional disability before and after the intervention period. The findings are expected to clarify whether one exercise approach provides superior improvements in patient outcomes and functional recovery. The results of this study will contribute to evidence-based physiotherapy practice by providing comparative evidence on two widely used rehabilitation protocols. Identifying the more effective intervention may assist physiotherapists in selecting appropriate exercise programs, improving clinical decision-making, optimizing rehabilitation outcomes, and supporting the development of standardized conservative management strategies for individuals with chronic non-specific low back pain.

Interventions

BEHAVIORALMcGill Stabilization Exercise Protocol

A progressive exercise program consisting of McGill stabilization exercises aimed at enhancing core muscle endurance, spinal stability, and neuromuscular control while reducing pain and improving lumbar function in individuals with chronic non-specific low back pain.

BEHAVIORALSahrmann's Exercise Protocol

A progressive movement-based exercise program designed to improve motor control, activate deep stabilizing muscles, correct faulty movement patterns, and enhance functional performance in individuals with chronic non-specific low back pain.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)

Masking description

Single (Outcome Assessor)

Intervention model description

Participants will be randomly assigned to one of two parallel intervention groups. One group will receive the McGill stabilization exercise protocol, while the other group will receive the Sahrmann's movement-based exercise protocol. Both groups will receive their assigned intervention concurrently throughout the study period, and outcomes will be compared between the groups to determine the relative effectiveness of the two exercise protocols in improving pain, lumbar range of motion, and functional disability in individuals with chronic non-specific low back pain.

Eligibility

Sex/Gender
ALL
Age
20 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Adults aged 20-50 years. * Male and female participants. * Diagnosed with chronic non-specific low back pain lasting more than 12 weeks. * Pain intensity of 3-4 on the Numeric Pain Rating Scale (NPRS) at baseline. * Able and willing to participate in the exercise program and attend all treatment sessions. * Willing to provide written informed consent.

Exclusion criteria

* History of spinal surgery. * Presence of neurological deficits. * Structural spinal deformities. * Pregnancy or within 6 months postpartum. * Presence of red flag signs or systemic illness (e.g., fracture, infection, malignancy, inflammatory disorders). * Individuals unable or unwilling to participate in the exercise program or complete the study protocol.

Design outcomes

Primary

MeasureTime frameDescription
1. Numeric Pain Rating Scale (NPRS)[Time Frame: 6 Weeks]Pain intensity will be assessed using the Numeric Pain Rating Scale (NPRS). The NPRS is a valid and reliable self-reported pain assessment tool that measures pain intensity on an 11-point scale ranging from 0 ("no pain") to 10 ("worst imaginable pain"). Participants will be asked to select the number that best represents their current pain intensity. A decrease in the NPRS score indicates an improvement in pain following the intervention.
2. Oswestry Disability Index (ODI)[Time Frame: 6 Weeks]Functional disability will be assessed using the Oswestry Disability Index (ODI). The ODI is a disease-specific, validated questionnaire used to evaluate disability associated with chronic low back pain. It consists of 10 sections covering pain intensity, personal care, lifting, walking, sitting, standing, sleeping, social life, travelling, and employment/homemaking. Each section is scored from 0 to 5, with higher total scores indicating greater disability. A reduction in the ODI score reflects improvement in functional status and daily activities.

Secondary

MeasureTime frameDescription
3. Bubble Inclinometer[Time Frame: 6 Weeks]Lumbar range of motion (ROM) will be measured using a bubble inclinometer, a reliable and valid instrument for assessing spinal mobility. Measurements will be obtained for lumbar flexion, extension, right and left lateral flexion, and right and left rotation according to standardized measurement procedures. The bubble inclinometer provides objective assessment of lumbar spinal movement in degrees. An increase in lumbar range of motion indicates improvement following the intervention.

Countries

Pakistan

Contacts

CONTACTImran Amjad, Phd
imran.amjad@riphah.edu.pk03324390125
PRINCIPAL_INVESTIGATORAnnum Manzoor, MS OMPT

Gulab Devi Teaching institute

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 25, 2026