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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04942782
Other study ID # p.t.REC/012/003225
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date July 1, 2021
Est. completion date August 1, 2021

Study information

Verified date June 2021
Source Cairo University
Contact al shaymaa sh abd el azeim, lecturer
Phone 01033771553
Email alshaymaa.shaaban@pt.cu.edu.eg
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the purpose of this trial is to investigate and compare between lumbopelvic stabilization and pilates exercises on gait cycle phases and maximum peak pressure on the foot in chronic nonspecific low back pain?


Description:

LBP is the leading cause of activity limitation, results in significant losses in productivity at work, and incurs billions of dollars in medical expenditure annually So, the aim of physical therapy treatment in the patient with chronic nonspecific low back pain is more effective in improving gait cycle phases and maximum peak pressure on the foot and help LBP patients to walk normally as much as possible, also this will improve our body of knowledge about the best modalities for treating LBP. The finding of this study may help LBP patients avoid exposure to complications due to altered gait cycle phases and maximum peak pressure on the foot. Also, it will help physiotherapists to know which treatment will be effective in improving gait cycle phases and maximum peak pressure on the foot. one hundred patients with mechanical low back pain will be allocated randomly to three groups; group A will receive pilates, group B will receive lumbopelvic stabilization exercise and group C will receive strengthening exercises for the abdominals, back, and hip muscles


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date August 1, 2021
Est. primary completion date August 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: 1. Their age between 20 and 40 years 2. patients is required to have chronic nonspecific LBP (more than12 weeks), de?ned as Pain in the lumbar and/or buttock region (defined as pain reported below the level of T12 and no lower than the buttock line). 3. Patients will be excluded if they have signs of serious spinal pathology (red flags) including significant trauma, unexplained weight loss, and widespread neurologic changes Exclusion Criteria: 1. subjects with specific back pain (fracture, osteoporosis or degenerative changes, prolapse intervertebral disc, bone disorders, arthritis, tumour), 2. subjects with neurological involvement (radiculopathy, myelopathy), 3. subjects with previous spinal surgery

Study Design


Related Conditions & MeSH terms


Intervention

Other:
lumbopelvic stabilization exercises
the patients will receive lumbopelvic stabilization in the form of three parts: 1 Segmental control over primary stabilizers (mainly TrA, deep multifidus, pelvic floor and diaphragm) 2-Exercises in closed chain, with low velocity and low load 3-Exercises in open chain, with high velocity and load
pilates exercise
the patient will receive pilates exercise in the form of Breast stroke prep, Side leg lift series, One leg circle, Hundreds, Shoulder bridge, and Spine stretch forward
conventional therapy
Patients will received strengthening exercises for the abdominal, back, and hip muscles. The patients performed an average of three series of ten repetitions of each exercise. Increases in the number of exercises performed in each session (or load progression) occurred according to individual tolerance

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Outcome

Type Measure Description Time frame Safety issue
Primary gait cycle phases and maximum peak pressure on foot gait cycle phases and peak pressure will be measure by Tekscan walkway up to twelve weeks
Secondary pain intensity visual analogue scale will be used for measuring pain level up to twelve weeks
Secondary disability Functional disability of each patient was assessed by Modified Oswestry Disability Questionnaire up to twelve weeks
Secondary muscle endurance Sorensen test (low back fatigue test) and Trunk flexion endurance test will be used for measuring the level of endurance up to twelve weeks
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