NCT06773247

Brief Summary

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.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 2, 2025

Completed
1 day until next milestone

Study Start

First participant enrolled

January 3, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

January 14, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 3, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

April 3, 2025

Completed
Last Updated

January 14, 2025

Status Verified

December 1, 2024

Enrollment Period

2 months

First QC Date

January 2, 2025

Last Update Submit

January 8, 2025

Conditions

Keywords

Myofascial Release, Cupping, NSLBP

Outcome Measures

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

    4 weeks

Secondary Outcomes (1)

  • Functional Disability

    4 weeks

Other Outcomes (1)

  • Assessment procedure of lumbar flexion and extension ROM

    4 weeks

Study Arms (1)

Myofascial Release Technique

EXPERIMENTAL

Vertical stroking technique was performed in lumbar region to quadratus lumborum. Activities like sustained repetitive movements, twisting, bending, sedentary posture for prolonged duration, muscle imbalance, etc. leads to trigger point formation making quadratus lumborum as a common source of low back pain. It 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.

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

Interventions

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

Myofascial Release Technique

Eligibility Criteria

Age45 Years - 55 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • 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 .

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Physical Therapy, Cairo University.

Cairo, Egypt, 12518, Egypt

Location

Study Officials

  • Rabab M Shoala, PHD

    Basic Science Department, Faculty of Physical Therapy, Cairo University, Egypt.

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Rabab M Assistant Professor of Physical Therapy, PHD

CONTACT

Rabab M Assistant Professor of Physical Therapy, PHD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Masking Details
Masking Description
Purpose
TREATMENT
Intervention Model
SINGLE GROUP
Model Details: Model Description
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor of Physical Therapy

Study Record Dates

First Submitted

January 2, 2025

First Posted

January 14, 2025

Study Start

January 3, 2025

Primary Completion

March 3, 2025

Study Completion

April 3, 2025

Last Updated

January 14, 2025

Record last verified: 2024-12

Locations