Global Postural Reeducation Versus Pilates in Patients With Non-specific Low Back Pain
LBP
1 other identifier
interventional
60
0 countries
N/A
Brief 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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable low-back-pain
Started Jun 2025
Shorter than P25 for not_applicable low-back-pain
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 24, 2025
CompletedStudy Start
First participant enrolled
June 30, 2025
CompletedFirst Posted
Study publicly available on registry
July 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2025
CompletedJuly 2, 2025
June 1, 2025
3 months
June 24, 2025
June 24, 2025
Conditions
Keywords
Outcome Measures
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)
up to six weeks
Secondary Outcomes (4)
disability
up to six weeks
anterior pelvic tilt
up to six weeks
lumbar lordosis
up to six weeks
hip flexor flexibility
up to six weeks
Study Arms (3)
global postural reeducation exercise
EXPERIMENTALTwenty 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
pilates exercises
EXPERIMENTALTwenty patients suffer from nonspecific low back pain and will receive Pilates exercise and conventional physiotherapy treatment two times a week for six weeks
conventional therapy
ACTIVE COMPARATORTwenty patients suffer from nonspecific low back pain and will receive conventional physiotherapy treatment two times a week for six weeks.
Interventions
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
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
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).
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Masking Details
- opaque sealed envelope
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- principle investigator : ibrahim mostafa mohamed
Study Record Dates
First Submitted
June 24, 2025
First Posted
July 2, 2025
Study Start
June 30, 2025
Primary Completion
September 30, 2025
Study Completion
September 30, 2025
Last Updated
July 2, 2025
Record last verified: 2025-06