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Not yet recruitingNCT07047287LBPUpdated Jul 2, 2025

Global Postural Reeducation Versus Pilates in Patients With Non-specific Low Back Pain

An interventional study of global postural reeducation exercise and pilates exercises in Low Back Pain, sponsored by Cairo University. Not yet recruiting. Open to participants aged 18 Years to 50 Years. Per ClinicalTrials.gov, last updated 2025-07-02.

Sponsored by Cairo University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Sep 2025, 1 year ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years to 50 Years
Sex
All
01

Study summary

to compare between Global Postural Reeducation and Pilates mat on pelvic angles, pain intensity, hip flexibility and Functional disability in patients with chronic non-specific low back pain

Read the detailed description

Chronic low back pain is a common health problem in many developed and developing countries. Individuals suffering from chronic low back pain experience major physical, social, mental, and occupational disruptions. It is not only one of the leading causes of pain but also of a costly burden on the health care budget as chronic low back pain leads to a frequent demand for medical services. The majority of patients (up to 90%) are categorized as having nonspecific low back pain.Global postural reeducation (GPR) is a conservative treatment that we can consider as a global postural exercise method, and widely used in physical therapy clinical practice in many countries. Pilates is a concept of body and mind exercise and a system of repetitive exercises including whole-body movements, breathing, centering, rhythm, and concentration. Pilates is a mindful approach exercise that promote strength, stability and is used for health enhancement and in several diseases.

02

Conditions studied

  • Low Back Pain

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Keywords

  • global postural reeducation
  • pilates
  • low back pain
03

In context

Low Back Pain

2,818 studies on the registry are indexed under Low Back Pain; 482 are open to participants now.

This study's planned enrollment of 60 is close to the median of 60 across 2,268 interventional studies indexed under Low Back Pain.

Browse Low Back Pain studies →

Lead sponsor

Cairo University is the lead sponsor of 4,780 studies on the registry; 1,427 are open to participants now.

Of its 36 completed or terminated interventional studies of FDA-regulated products, 5 (14%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 18-50 years old, Low back pain for more than 3 months (pain felt between T12 and the gluteal fold).
  • Patients willing and able to participate in an exercise program safely and without cognitive impairments that would limit their participation.
  • BMI index smaller than 30 kg/m2
  • Both male and female gender were included in the study.
  • Nonspecific, non-radicular (axial) chronic LBP diagnosis (LBP for at least three months).
  • Visual Analog Scale (VAS) score of 3 or higher

Exclusion criteria

Exclusion Criteria:

  • History of back surgery
  • Rheumatologic disorders,
  • Spine infections
  • Spine exercise training in the 3 months before the onset of the study.
  • Under psychiatric care.
  • Neurological conditions that would interfere with the assessments, such as major sensory changes, and level of consciousness/ understanding
  • Advanced joint disease.
  • History of severe physical and nervous system diseases
  • Unable to cooperate with the study protocols.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Experimental
    global postural reeducation exercise

    Twenty patients suffer from nonspecific low back pain and will be received Global postural reeducation exercise and conventional physiotherapy treatment two times a week for six weeks

    Other: global postural reeducation exercise · Other: conventional therapy

  • Experimental
    pilates exercises

    Twenty patients suffer from nonspecific low back pain and will receive Pilates exercise and conventional physiotherapy treatment two times a week for six weeks

    Other: pilates exercises · Other: conventional therapy

  • Active comparator
    conventional therapy

    Twenty patients suffer from nonspecific low back pain and will receive conventional physiotherapy treatment two times a week for six weeks.

    Other: conventional therapy

Interventions

  • Otherglobal postural reeducation exercise

    The global postural reeducation exercise involves a sequence of active, moderate postures as well as exercises that are designed to realign joints, stretch shortened muscles, in addition, strengthen the contraction of the antagonist's muscles to prevent postural asymmetry. There are eight different therapeutic postures in the GPR approach that should be held for 15 to 20 min while lying, sitting, or standing. Only two or three postures have been proposed to encourage treatment standardization+ conventional therapy

  • Otherpilates exercises

    the patients will receive pilates in the form of single leg stretch + Pelvic press + Swimming + Opposite arm and leg reach + Side to side), 3 sets of 10 repetitions

  • Otherconventional therapy

    the patients will receive conventional physiotherapy treatment which consists of routine physical therapy eg. (Back, hamstring, calf and hip flexors stretches, Abdominal curl up exercises etc along with ultrasound and Transcutaneous electrical nerve stimulation (TENS).

06

What researchers measure

Primary outcomes

  1. pain intensity

    VAS is employed as a quantitative tool to assess the subjective intensity of pain experienced by an individual. The VAS is a reliable and valid method for assessing low back pain clinically. It consists of a single handwritten mark down the length of a 10-cm line, with "no pain" at one end of the scale (0 cm) and "worst pain" at the other (10 cm)

    Time frame: up to six weeks

Secondary outcomes

  1. disability

    The Arabic version of the Oswestry Disability Index (ODI) has been applied to evaluate the disability brought reliability. The questionnaire was filled out by the patient in about 5 min, and the doctor scored it in around 1 min. Each component is given a score between 0 and 5, with 5 being the most severe disability. The index is determined through the division of the total score by the range of scores, and then its numerical representation as a percentage is derived by multiplying the result by 100. As a result, the denominator drops by 5 for each query that is unanswered

    Time frame: up to six weeks

  2. anterior pelvic tilt

    Using the iHandy Level app on a smartphone will be used to assess anterior pelvic tilt. The anterior and posterior iliac spines were felt. The iHandy's angle was set to 0 while the patient was lying prone, and a semi-permanent pen was used to mark the skin at levels L5-S1.The patient was lying in a long sitting position with his or her feet flat against a wall. The examiner instructed the patient to move their ischial tuberosities into a more posterior position and to raise their chest towards the wall. Try to stay at the same height while you move forward from the hips. Proceed as far as you are able to. Stop when you feel you can no longer go or when your knees start to lift under your hands. Instead of bouncing, hold as tightly as you can. There were only 10 s in this pose.

    Time frame: up to six weeks

  3. lumbar lordosis

    flexible ruler will be used to assess lumbar lordosis. To get an accurate reading of lumbar lordosis, a flexible ruler is employed. The flexible ruler demonstrates high reliability and validity as a portable and non-invasive tool for measuring lumbar lordosis. Specifically, the validity of lumbar lordosis measures obtained using the flexible ruler, when compared to those obtained using X-ray imaging, is reported to be 0.91. An angel's theta can be calculated using the formula \[theta\]=4×\[arctan(2H/L)\], where theta stands for the magnitude of the lordotic curve. The lumbar lordotic angle typically ranges from 6.50 to 17.80°.

    Time frame: up to six weeks

  4. hip flexor flexibility

    hip flexor flexibility will be used to assess hip flexor flexibility. The modified Thomas test has been used to evaluate hip flexor flexibility. The patient was lying on their back during this test, and their thigh was hanging over the side of the examination table. The patient firmly held the thigh of the unexamined limb and brought it closer to their chest. The pelvis was rotated posteriorly, and the lumbar spine was flat on the plinth. Using a goniometer to measure the angle of hip flexion, the length of the iliopsoas muscle was determined. The femur's greater trochanter and fulcrum were in line. Using the pelvis as a reference point, the measurement was performed by positioning the goniometer's fixed arm along the lateral midline of the abdomen and its moving arm along the lateral midline of the femur.

    Time frame: up to six weeks

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 2, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07047287
Lead sponsor
Cairo University
Responsible party
ibrahim mostafa mohamed (principle investigator : ibrahim mostafa mohamed, Cairo University) — Principal investigator
First posted
Jul 2, 2025
Start date
Jun 30, 2025 (estimated)
Primary completion
Sep 30, 2025 (estimated)
Completion
Sep 30, 2025 (estimated)
Last update
Jul 2, 2025

Study contacts

ibrahim mostafa, master
Contact
Ielmoniry@gmail.com
01111314524

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Jun 2025. You cannot join it, but the record below documents what was studied.

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