Mulligan SNAG Technique in Individuals With Lumbar Intervertebral Disc Protrusion

NCT ID: NCT06521294

Last Updated: 2025-04-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

ACTIVE_NOT_RECRUITING

Clinical Phase

NA

Total Enrollment

38 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-02-16

Study Completion Date

2026-01-15

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study aimed to examine the effects of the Mulligan SNAG mobilization technique, applied in addition to conventional physiotherapy on the structure of the intervertebral disc and physical functioning in patients diagnosed with low back pain due to lumbar intervertebral disc protrusion. 38 volunteer patients will participate in the study. The participants will be randomized as an interventional and control gropus.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Participants will be treated 3 days a week for 4 weeks. The session duration will be 40-45 minutes. Visual analog scale-VAS, oswestry disability index, magnetic imaging-MRI assessment, functıonal independence scale-FIM, Tampa kinesiophobia scale, one leg stand test, sit-stand test, 10-meter walking test, cadence , Nottingham health profile will be used to assses the participants in the two groups. All participants will be evaluated in the 5th week of the study. The program includes physical therapy session (Hot packed, trans cuteneal electric stimulation, therapeutic ultrasound, and therapautic exercises) and the Mulligan SNAG mobilization technique.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Intervertebral Disc Protrusion

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Randomized controlled trial
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Group 1

SNAG

Group Type EXPERIMENTAL

Mulligan SNAG mobilization tecnique

Intervention Type OTHER

Mulligan SNAG mobilization tecnique

Conventional Physiotherapy

Intervention Type OTHER

Conventional Physiotherapy

Group 2

Physiotherapy

Group Type ACTIVE_COMPARATOR

Conventional Physiotherapy

Intervention Type OTHER

Conventional Physiotherapy

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Mulligan SNAG mobilization tecnique

Mulligan SNAG mobilization tecnique

Intervention Type OTHER

Conventional Physiotherapy

Conventional Physiotherapy

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

1. Being between the ages of 20-60
2. Those diagnosed with lumbar intervertebral disc heniation (protrusion on L1-L2, L2-L3, L3-L4, L4-L5, L5-S1) at a single level
3. Those who voluntarily agreed to participate in the study

Exclusion Criteria

* Individuals diagnosed with Lumbar Bulging, Extruded, Sequestered discs
* Individuals who have undergone lumbar region spinal surgery
* Individuals with spinal deformity (scoliosis, spondylolisthesis, Ankylosing Spondylitis)
* Individuals with lumbar stenosis
* Pregnant women
* Individuals receiving treatment for malignancy (primary or metastatic tumoral conditions in the lumbar region)
* Individuals diagnosed with advanced osteoporosis
* Individuals diagnosed with discitis
Minimum Eligible Age

20 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Biruni University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Ugur Cavlak

CLINICAL PROFESSOR

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

UGUR CAVLAK, Prof.

Role: PRINCIPAL_INVESTIGATOR

Biruni University

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Faculty of Health Sciences in Biruni University

Istanbul, ZEYTINBURNU, Turkey (Türkiye)

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Turkey (Türkiye)

References

Explore related publications, articles, or registry entries linked to this study.

Hussien HM, Abdel-Raoof NA, Kattabei OM, Ahmed HH. Effect of Mulligan Concept Lumbar SNAG on Chronic Nonspecific Low Back Pain. J Chiropr Med. 2017 Jun;16(2):94-102. doi: 10.1016/j.jcm.2017.01.003. Epub 2017 Mar 30.

Reference Type BACKGROUND
PMID: 28559749 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

BiruniUniversity34

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Non-Specific Chronic Low Back Pain Treatment Methods
NCT07057687 ACTIVE_NOT_RECRUITING NA