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

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05953922
Enrollment
50
Registered
2023-07-20
Start date
2022-10-01
Completion date
2023-09-30
Last updated
2023-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non Specific Low Back Pain

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.

Interventions

OTHERcore stability exersises

core stability exercises and transcutaneous electrical nerve stimulation for four week three session per week

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Intervention model description

intervention study

Eligibility

Sex/Gender
FEMALE
Age
22 Years to 45 Years
Healthy volunteers
No

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 * sever cardio vascular or metabolic disease * history of psychological disease * anatomical and congenital disturbance * continuous pain more than 8 on (visual analogue scale)

Design outcomes

Primary

MeasureTime frameDescription
quality of life for each participantsbaselineWe will use the Arabic version of world health organization's quality of life (Arabic\_WHOQOL-BREF) questionnaire and higher score means better outcome
pain levels for each participantsbaselinevisual analogue scale will be used to assess the level of pain and higher score means worse outcome
pressure lumber biofeedback for each participantsbaselinepressure lumber biofeedback for asses transverse abdominis contraction

Countries

Egypt

Contacts

Primary ContactWafaa A. Salama Ashour, Bachelor's
pt.w.ahmedashour@gmail.com01008983388

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026