NCT07047287

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

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
60

participants targeted

Target at P50-P75 for not_applicable low-back-pain

Timeline
Completed

Started Jun 2025

Shorter than P25 for not_applicable low-back-pain

Status
not yet recruiting

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

Completed
6 days until next milestone

Study Start

First participant enrolled

June 30, 2025

Completed
2 days until next milestone

First Posted

Study publicly available on registry

July 2, 2025

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 30, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 30, 2025

Completed
Last Updated

July 2, 2025

Status Verified

June 1, 2025

Enrollment Period

3 months

First QC Date

June 24, 2025

Last Update Submit

June 24, 2025

Conditions

Keywords

global postural reeducationpilateslow back pain

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

EXPERIMENTAL

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 exerciseOther: conventional therapy

pilates exercises

EXPERIMENTAL

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 exercisesOther: conventional therapy

conventional therapy

ACTIVE COMPARATOR

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

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

global postural reeducation exercise

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

pilates exercises

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).

conventional therapyglobal postural reeducation exercisepilates exercises

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

MeSH Terms

Conditions

Low Back Pain

Interventions

Exercise Movement Techniques

Condition Hierarchy (Ancestors)

Back PainPainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Physical Therapy ModalitiesTherapeutics

Central Study Contacts

ibrahim mostafa, master

CONTACT

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
Model Details: global postural reeducation and pilates
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