INFLUENCE OF COMBINED INTERFERENTIAL CURRENT STIMULATION AND ABDOMINAL DRAW-IN EXERCISES IN THE TREATMENT OF CHRONIC NON-SPECIFIC LOW BACK PAIN

Not Applicable

Recruiting

• Conditions: to Investigate Influence of a Combined Interferential Current Stimulation and Abdominal Draw -in Exercises in Patients With Chronic n
• Interventions: Device: Interferential current stimulation; Other: Draw- In exercises,,

• Registration Number: NCT06066567
• Lead Sponsor: Cairo University

Brief Summary

The purpose of this study is to investigate influence of a combined interferential (IF) current stimulation and abdominal draw-in exercises on the abdominal muscle thickness, TrA endurance, pain intensity and function disability in patients with chronic non-specific LBP (CNSLBP) CNSLBP is considered the second most common health problem after headache. The lifetime of LBP among Egyptian patients in a family center reached 48%, which indicates that LBP is a prevalent symptom that deserves more attention.

One hypothesis for the development of LBP is due to a dysfunction in the control of the abdominal and back muscles and this change in spinal control is due in part to in local segmental muscles dysfunction, such as the transversus abdominis (TrA). Interferential therapy (IFT) is capable of achieving uniform stimulation and high reproducibility, it is thought to be less stressful, as well as enhance deep muscle contraction.

Also, there is the specific training of the TrA provided functional and therapeutic benefits, such as unloading of the spine, anticipatory postural control, intersegmental stabilization of the spine, and long-term pain relief. Draw-in is a typical TrA exercise.

Many studies have mainly focused on the morphological aspects of paraspinal muscles which play an essential role in patients with CNSLBP while our study focused on influence of a combined IFT stimulation and abdominal draw-in exercises on the abdominal muscle thickness, TrA endurance, pain intensity and function disability in patients with chronic non-specific LBP (CNSLBP

Detailed Description

60 patients suffering from chronic non-specific low back pain will participate in this study. Both sexes will participate in this study; aged 20-45 years. will be diagnosed and referred from Orthopedist. The study will be conducted at outpatient clinic of Deraya university Elmina government. The patients will be divided randomly into two groups equal in numbers (group A), (group B).

Group(A): (Experimental group) :( 30 patients will receive IFC stimulation, Draw In exercises from prone position, hot pack, back muscles stretching and strengthening exercises for the back and abdominal muscles).

Group(B): (control group) (30 patients will receive Draw In exercises from prone position, hot pack, back muscles stretching and strengthening exercises for the back and abdominal muscles).

Study Timeline

• Study First Submitted: 2023-09-27
• Study First Submitted QC: 2023-09-27
• Study First Posted: 2023-10-04
• Study Start: 2023-11-01
• Status Verified: 2024-01
• Last Update Submitted: 2024-01-03
• Last Update Posted: 2024-01-05
• Primary Completion: 2024-05-01
• Study Completion: 2024-06-01

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

• 60 patients with chronic non-specific low back pain (>3 months).
• 2. Age of participants will range from 20 to 45 years.
• 3.Both sexes will participate in this study.
• 4.Body mass index (BMI) will range from 25 to 29.9 (Kg / m2).

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Exclusion Criteria

• Subjects will be excluded from the study if they have previous spinal surgery, spinal cord injury or unstable neurological signs, Lumbar intervertebral disc, congenital postural deformities, inability to contract the abdominal muscles, cauda equine symptoms related to the spine including changes in bowel and bladder control, cardiac pacemaker, and females during pregnancy.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Experimental: treatment group	Interferential current stimulation	-
Experimental: treatment group	Draw- In exercises,,	-
control group	Draw- In exercises,,	-

Primary Outcome Measures

Name	Time	Method
Pain intensity	4 weeks	Pain intensity with visual analogue scale (VAS).
. Functional disability	4 weeks	Functional disability with Arabic version of Oswestry Disability Index (ODI).
Transverse abdominis (TrA) muscle endurance	4 weeks	Transverse abdominis (TrA) muscle endurance with prone endurance test guided by Pressure Biofeedback Unit (PBU).
Abdominal muscle thickness	4 weeks	TrA, External Oblique (EO) and Internal Oblique (IO) with Ultrasonography imaging examination.

Trial Locations

Locations (2)

Faculty of physical therapy; 🇪🇬 Giza, Egypt

Cairo University; 🇪🇬 Giza, Egypt