Effect of Lumbar Spine Correction Training on Postural Awareness and Stability in Patients With Low Back Pain

ConditionLow Back Pain
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age25-45
SponsorOctober 6 University

About this trial

PURPOSE: to investigate The Efficacy of lumbar spine correction training on postural awareness and stability in patients with low back pain. Patients with low back pain demonstrate impairments in function and range of motion to deficits in patient's quality of life.

HYPOTHESES: It will be hypothesized that there will be no statically Effect of lumbar spine correction training on postural awareness and stability in patients with low back pain

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Their ages range from 25 to 45 years.

Both sex

Low back pain for more than 6 months.

Normal body mass index (18.5 - 29 Kg/m2).

Disqualifiers

Patients with any other Neurological deficits, psychiatric disease lumbar myelopathy, Cognitive problems, vertebral fractures and previous history of spine or lumbar surgery.

Clinical instability, recent trauma

Structural abnormalities of the spine, osteoporosis, and spasmodic torticollis.

Inflammatory or other specific disorders of spina such as ankylosing spondylitis and rheumatoid arthritis

Trial design

Design model

Parallel

Treatments tested in this trial

  • lumbar spine correction training

    Other intervention

    The patients will be mainly trained with trunk control exercise inform of: the trunk muscle against gravity and a Swiss ball for training on an unstable surface. Also the program will include Postural correction exercise inform of: Abdominal drawing-in breathing, upper body raising, bridge exercise, quadruped and spinal extension exercises will carried out

  • conventional treatment

    Other intervention

    Therapeutic Ultrasound device with patient prone lying position paravertebral in posterior aspect of back, Transcutaneous Electrical Nerve Stimulation (TENS) in the prone position, the electrodes will be positioned on the patient's pain area with a frequency of 100Hz , Heat application: in the form of (hot packs) for 15 minutes on posterior aspect of back as the patient will be in prone lying position and Core strengthening exercises

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: lumbar spine correction trainingExperimental treatment 2 interventions
Group B: conventional treatmentExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

postural habits and awareness scale (PHAS)

The Postural Habits and Awareness Scale (PHAS) is a 19-item, 5-point Likert scale developed to assess individuals' self-perceived postural habits and their conscious awareness of posture Scoring: The scale is scored from 1 (completely disagree) to 5 (completely agree), with 7 items being reverse-coded. where higher scores indicate better postural habits and greater awareness.

Time frame
four weeks
2

Oswestry Low Back Pain Disability Questionnaire

The Oswestry Disability Index (ODI) a patient-completed questionnaire which gives a subjective percentage score of level of function (disability) in activities of daily living in those rehabilitating from low back pain. Each item consist of 6 statements which are scored from 0 to 5. With 0 indicating the least disability and 5 the greatest then the total score is calculated as a percentage, with 0% indicating no disability and 100% indicating the highest level of disability

Time frame
four weeks
3

multidirectional reach test

The Multi-directional reach test is an inexpensive, reliable, and valid tool for measuring the limits of stability as derived by reach in four directions. Values obtained on relatively healthy older adults serve as norms for screening patient populations

Time frame
four weeks

Secondary outcomes

1

visual analogue scale (VAS)

The visual analogue scale (VAS) is a validated, subjective measure for acute and chronic pain. Scores are recorded by making a handwritten mark on a 10-cm line that represents a continuum between "no pain" and "worst pain

Time frame
four weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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