Skip to content

Remission of Lumbar Disc Herniation by Physiotherapy

Lumbal Disk Herniasyonunda farklı Tedavi yöntemlerinin etkinliğinin karşılaştırılması

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02699164
Enrollment
20
Registered
2016-03-04
Start date
2014-01-31
Completion date
2015-06-30
Last updated
2016-08-16

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

Conditions

Lumbar Disc Herniation

Keywords

non surgical spinal decompression therapy, deep friction massage, exercise

Brief summary

This study was conducted with the aim of determining whether or not Non surgical spinal decompression therapy was effective in remission of herniation, decreasing pain and improving functional status.

Detailed description

Both groups received combination of electrotherapy, deep friction massage and stabilization exercise for fifteen session. Combine group received non surgical spinal decompression therapy (NSDT) different from conventional physiotherapy group. Numeric Analog Scale, Straight leg raise (SLR) test, Oswestry Disability Index (ODI) were applied at baseline and after treatment. Disc height and herniation thickness were measured on Magnetic Resonance Imagination (MRI) which performed at baseline and three months after therapy.

Interventions

DEVICEDRX 9000, Axiom Worldwide, Tampa, Florida

non-surgical spinal decompression therapy consist 18 traction cycles. Traction force applied herniation levels according to Magnetic Resonance Imaging (MRI).

OTHERphysiotherapy

electrotherapy was used. electrotherapy consisted of 20 minutes of hot-pack, 20 minutes of TENS and 5 minutes of ultrasound.

spinal stabilization exercises started elementary exercises. According to patient tolerance, exercise program reestablished.

Sponsors

Hacettepe University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
25 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

diagnosed as lumbar disc herniation suffering from low back pain at least 8 weeks

Exclusion criteria

undergone any spinal surgery clinical diagnosis of osteoporosis clinical diagnosis of scoliosis and spondylolisthesis any neurological disease causes sensorial loss

Design outcomes

Primary

MeasureTime frameDescription
herniation thicknesschange from baseline in herniation thickness and disc height at three monthsherniation thickness were measured on MRI.

Secondary

MeasureTime frameDescription
functionup to 3 monthsOswestry Disability Index was used.Oswestry Disability Index used to assess the changes in function and disability levels. Scores range from 0 to 100. scores between 0 and 20 described as minimal disability, scores between 21and 40 described as moderate disability,scores between 41and 60 described as severe disability,scores between 61 and 80 described as crippled and scores between 81 and 100 described as bed bounded
mobilityup to 3 monthsstraight leg raise test was used. Pain free angle of straight leg raise was measured with goniometer.
pain severitychange form baseline in pain severity at 15 sessions of treatmentnumeric analog scale was used. 0 described no pain, 10 described unbearable pain.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026