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Active, Not Recruiting

NCT Number: NCT06521294

Mulligan SNAG Technique in Individuals With Lumbar Intervertebral Disc Protrusion

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.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Age range

20 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Faculty of Health Sciences in Biruni University

Istanbul, ZEYTINBURNU, 34010, Turkey (Türkiye)

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Being between the ages of 20-60
  • Those diagnosed with lumbar intervertebral disc heniation (protrusion on L1-L2, L2-L3, L3-L4, L4-L5, L5-S1) at a single level
  • 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

Treatment and study plan

Mulligan SNAG mobilization tecnique

Other

Mulligan SNAG mobilization tecnique

Conventional Physiotherapy

Other

Conventional Physiotherapy

Primary outcomes

  1. Magnetic Resonance Imaging

    Time frame: baseline and iafter the intervention (in the 5th week)

    to measure protrusion (bigger amount means worse outcome)

  2. Visual Analog Scale-VAS

    Time frame: baseline and immediately after the intervention (in the 5th week)

    to measure pain intensity (min. score is 0 and max. score is 10- higher score means worse outcome)

Secondary outcomes

  1. Oswestry Disability Index-ODI

    Time frame: baseline and immediately after the intervention (in the 5th week)

    to describe disabilty level resulting from pain (min. score is 0 and max. score is 50- higher score means worse outcome)

  2. Functional Independence Measure- FIM

    Time frame: baseline and immediately after the intervention (in the 5th week)

    to measure independency in daily living activities (min. score is 18 and max score is 156- higger score means better independency in daily living activities)

  3. Tampa Kinesiophobia Scale- TKS

    Time frame: baseline and immediately after the intervention (in the 5th week)

    to measure anxiety-avoidance state (min. score is 17 and max. score is 68- higher score means worse outcome)

  4. One Leg stand Test- OLST

    Time frame: before and after the intervention (in the 5th week)

    to measure static balance ability (min. score 0 and max. score is 60- Higher score means better balance)

  5. Sit-Stand Test-SST

    Time frame: before and after the intervention (in the 5th week)

    to measure lower extremity performance (min. score is 0 and max. score is 30- higher score means better outcome)

  6. 10-m Walking test and cadance measurement

    Time frame: before and after the intervention (in the 5th week)

    to measure walking speed (in second- higher score means worse outcome) and cadance (number of steps during the test- higher score means better outcome)

  7. Nottingham Health profile-NHP

    Time frame: before and after the intervention (in the 5th week)

    to describe level of quality of life (min. score is 38 and max. score is 3800 - higher score means poor health)

Sponsors and collaborators

Lead sponsor

Biruni University

Other

Registry information

Official study title

Effect of the Mulligan SNAG Technique on Structure of Intervertebral Disc and Physical Functioning in Individuals With Lumbar Intervertebral Disc Protrusion: A Randomized Controlled Study

Important dates

Study start
2025
Primary completion
2025
Study completion
2026
First posted
Jul 25, 2024
Registry last updated
Apr 6, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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