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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05334394
Other study ID # E-10840098-772.02-2868
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date July 10, 2021
Est. completion date February 15, 2022

Study information

Verified date April 2022
Source Medipol University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was aimed to investigate the effectiveness of mulligan mobilization technique on balance, pain and functionality in patients with chronic low back pain and to compare it with exercise.37 patients aged between 18-65 who applied to Fındıkzade Medipol Hospital were included in the study. The individuals participating in the study were divided into two groups, 18 control and 19 mulligan groups, according to the randomization table. The intervention was performed 3 times a week for 4 weeks. Conventional physiotherapy and exercise program accompanied by a physiotherapist were applied to the control group, and conventional physiotherapy and mulligan mobilization technique were applied to the mulligan group. Conventional physiotherapy methods included ultrasound (US), Transcutaneous Electrical Nerve Stimulation (TENS), and hotpack. The patients were evaluated with TecnoBody Static Balance Device, algometer, electrogoniometer, visual analog scale, Oswestry Low Back Pain Disability Questionnaire before and after the treatment.


Recruitment information / eligibility

Status Completed
Enrollment 37
Est. completion date February 15, 2022
Est. primary completion date February 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - Experiencing non-specific chronic low back pain for more than 3 months - The diagnosis has been confirmed by the Health Board Report - Be over 18 years old - Be younger than 65 years old - Pain of at least 2 severity according to VAS - Voluntarily agree to participate in the study Exclusion Criteria: - Previous lumbar trauma or operation - Long-term use of corticosteroids - Cancer - Pregnancy - Osteoporosis - Systemic Diseases - Spinal Deformities - Lumbal Stenosis - Ankylozone Spondylitis - Spondylolisthesis - Spinal Deformities - Lumbal Stenosis

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Mulligan Technique
Mulligan suggested that injuries or sprains can cause a minor positional error in a joint, thereby causing limitations in physiological movement. Unique to this concept is mobilization of the spine while weight bearing and directing the mobilization parallel to the spinal facet planes. Although it includes various mobilization techniques, one of the most important techniques, motion co-mobilization, is the SNAG's technique, which includes the application of accessory passive gliding to the lumbar vertebra while the patient performs active movement simultaneously.
Exercise Therapy
Exercise is recommended by physical therapists for most chronic low back pain patients.

Locations

Country Name City State
Turkey Findikzade Medipol Hospital Istanbul Findikzade

Sponsors (1)

Lead Sponsor Collaborator
Medipol University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary TecnoBody Static Balance Device Measurements TecnoBody Stability Easy is a stabilometric system consisting of three highly sensitive sensors. The system is based on continuous observation of the foot pressure center (COP). By recording the postural oscillations of the body as a function of time, detailed information about the postural system is obtained 5 Minutes
Primary Pressure Pain-Threshold Measurements with Algometer It is a device used to evaluate the sensitivity to pain and to determine the perception of pressure. The pressure algometer has proven useful in evaluating fibrositis and hypersensitive spots, trigger points, arthritis activation, and visceral pain-pressure sensitivity. 5 Minutes
Primary Electrogoniometer It is an evaluation tool used to record the objective measurement of joint range of motion. 5 Minutes
Secondary Visual Analog Scale Visual Analog Scale (VAS) is used to convert some values that cannot be measured numerically into digital. Two end definitions of the parameter to be evaluated are written on both ends of a 100 mm line and the patient is asked to indicate where his / her condition is appropriate by drawing a line or by placing a dot or marking. 1 Minutes
Secondary Oswestry Disability Index The Oswestry Disability Index is a commonly used outcome measure to detect perceived disability in patients with low back pain. It consists of 10 questions, each of which is scored between 0 and 5, assessing the degree of pain, personal care, lifting, walking, sitting, standing, sleeping, social life, traveling, and change in pain. The minimum score obtained from the scale is 0, and the maximum score is 50. 0-4 points as no disability, 5-14 points as mild, 15-24 points as moderate, 25-34 points as severe and 35-50 points as complete functional disability. 10 Minutes
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