Effectiveness of Myofascial Release Versus Dry Cupping in Management of Non-Specific Low Back Pain

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age45-55
SponsorCairo University

About this trial

Objective: The aim of this study was to compare the differences between the effect of myofascial release technique versus cupping technique on pain intensity level, spinal mobility and functional disabilities level in patients with NSLBP.

Methods: The study participants were 60 patients from both genders diagnosed as NSLBP. Their age ranged from 45 to 55 years old. They were assigned randomly into two groups: Group A (MFR): 20 patients received MFR and conventional physical therapy treatment. Group B: 20 patients received cupping technique and conventional physical therapy treatment. Group C: 20 patients received conventional physical therapy treatment only. All groups received treatment protocols three times a week for 4 consecutive weeks.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

patients age ranged from 45 to 55 years old and body mass index of 18.5-24.9 (kg/m2) with NSLBP of 3 or more month's duration.

All patients reported pain score of 4-6 based on the visual analog scale (VAS). 3.Patient with limitation in range of motion of lumbar spine due to tightness of the muscles, hypersensitive tender points on palpation along with pain localized para spinally .

Disqualifiers

Patients presented with lumbar radiculopathy

spinal pathology (fracture or tumors) or history of any spinal surgery

lumbar canal stenosis, osteoporosis

pregnancy related back pain, and spinal deformities like scoliosis or kyphosis.

Trial design

Design model

Single group

Treatments tested in this trial

  • I. Myofascial Release Technique ,Cupping Technique and II. Conventional Physical Therapy

    Other intervention

    The cupping procedure was performed as follows: Massage oil was applied over the area first to improve contact and makes it easier to move the cup's position. double-walled glass cups (6 glasses with diameters from 75 to 100 mm) were held inverted, after which each glass was placed on an afflicted area overlying the low back muscle (acupoint: BL23). Myofascial Release Technique Vertical stroking technique was performed in lumbar region to quadratus lumborum. AIt was performed as follow; Quadratus lumborum is palpated in prone and side lying for trigger points. The technique is applied by the patient positioned in side lying with a pillow under waist to exaggerate stretch of the muscle. The therapist stands at level of patient's hip posterior and counter pre

Treatment groups

60 Participants
are divided into 1 treatment group
Group A: Myofascial Release TechniqueExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

pain in low back area

Visual analog scale (VAS) was used to assess the intensity of perceived pain pre and post treatment in patients with NSLBP. The VAS is a reliable and valid tool for the quantification of perceived pain

Time frame
4 weeks

Secondary outcomes

1

Functional Disability

Level of daily living activities was measured using Oswestry Disability Index (Ar-ODI).The questionnaire contains 10 items related to limitations in daily life activities (like personal care, lifting, walking, sitting, standing, sleeping, social life, traveling, and work).Each item includes six potential responses that are rating on a 0 to 5 points scale, with maximum scores of ''5'' or ''total disability'' and a minimum score of ''0'' or ''no disability.'' 39-41 The total score is calculated as follows: (patient' score/50) \*100 to obtain the score expressed in percentage

Time frame
4 weeks

Other outcomes

1

Assessment procedure of lumbar flexion and extension ROM

Two inclinometers were used to measure lumbar flexion and extension. The examiner stood behind the standing subject. The skin was marked along the spine midway between two posterior superior iliac spines (PSIS), and one mark was made on the spinous processes, 15 cm superior to the PSIS line. Both inclinometers were placed over the skin marks.

Time frame
4 weeks

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