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Clinical Trials/NCT05953922
NCT05953922
Recruiting
Not Applicable

Effect of Core Stability Exercises on Pain and Quality of Life in Non Specific Low Back Pain

Cairo University1 site in 1 country50 target enrollmentOctober 1, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Non Specific Low Back Pain
Sponsor
Cairo University
Enrollment
50
Locations
1
Primary Endpoint
pressure lumber biofeedback for each participants
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

Most publications state that core stability exercises (transverse abdominis and multifidus training) can relieve chronic low back pain with or without radiculopathy and improve function, although only temporarily, and may have the same impact as active general exercise so The goal of this study is to detect the effect of retraining the deep core muscles, on pain, disability, and quality of life in patients with chronic Non specific low back pain.

Detailed Description

The goal of this study is to detect the effect of retraining the deep core muscles, on pain, disability, and quality of life in patients with chronic Non specific low back pain This study is delimited to the following aspects: 1. Fifty, patients of only females with chronic non specific low back pain more than 3 months. 2. The age will range from 22 to 45 years. 3. The treatment will conduct to three session per week for four weeks . 4. The selected patients will assigned randomly to two equal groups: 1- Group1 (intervention), will do the selected treatment that include electrical stimulation in addition to Core stability exercises program. 2- Group2(control), will do the conventional treatment only.

Registry
clinicaltrials.gov
Start Date
October 1, 2022
End Date
September 2023
Last Updated
2 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Wafaa Ahmed Salama Ashour

physical therapist

Cairo University

Eligibility Criteria

Inclusion Criteria

  • gender is women
  • age ranges from 22 to45 years old
  • chronic non specific low back pain for at least 3 month
  • pain score will between 3 to 6 on visual analogue scale

Exclusion Criteria

  • Any deformity of the spine
  • Red flags including serious pathology
  • Systemic or inflammatory disease
  • sever osteoporosis
  • history of tumor or cancer
  • spine infection
  • history of spine or pelvis surgery or fracture
  • cauda equina syndrome
  • progressive neurological deficit
  • severe instability

Outcomes

Primary Outcomes

pressure lumber biofeedback for each participants

Time Frame: baseline

pressure lumber biofeedback for asses transverse abdominis contraction

pain levels for each participants

Time Frame: baseline

visual analogue scale will be used to assess the level of pain and higher score means worse outcome

quality of life for each participants

Time Frame: baseline

We will use the Arabic version of world health organization's quality of life (Arabic_WHOQOL-BREF) questionnaire and higher score means better outcome

Study Sites (1)

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