AzTrials
AzTrials

Low Back PainNCT07552064

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

A study testing lumbar spine correction training and conventional treatment in people with Low Back Pain, run by October 6 University.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Official record
Search all trials

Trial summary

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. Read more about this study

Who is it for?
Ages 25 to 45 years
Conditions the study is for
Low Back Pain
What is being tested?
lumbar spine correction training and conventional treatment
Could I receive a placebo?
No, everyone receives an active treatment
How many people
30 participants
Where
No sites listed yet
Study dates
30 Apr 2026to 30 Jul 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 25 to 45 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • 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).

Who cannot join

  • 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

About this study

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

Read the detailed description

Progressive postural control exercise (PPCE) including lumbar correction training, is a novel strategy for patients with LBP. It originates from motor control exercise and resistance training with a theme of challenging postural control with phased progression, a beneficial effect for strength or resistance and coordination or stability exercise programs over other interventions be used in the treatment of LBP. Motor control exercises were also reported to produce slightly better short-term function and perceptions of an effect than general exercise in patients with chronic non-specific back pain. The progression of the training load was suggested to improve postural control in young individuals as it was better on neuromuscular plasticity than general exercise

Conditions
Low Back Pain
Being tested
lumbar spine correction training, conventional treatment
Medical subject headings
Low Back Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • lumbar spine correction trainingOther

    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 treatmentOther

    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

Study groups in NCT07552064
Study groupRoleWhat they receive
lumbar spine correction trainingExperimentallumbar spine correction training
Receives: Other: lumbar spine correction training; Other: conventional treatment
conventional treatmentExperimentalconventional treatment
Receives: Other: conventional treatment

What is being measured

The primary outcome is the main question the study is designed to answer.

  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.

    Measured: 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

    Measured: 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

    Measured: four weeks

Secondary outcomes (1)
  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

    Measured: four weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted27 Apr 2026
  2. Study start30 Apr 2026 (estimated)
  3. Primary completion15 Jul 2026 (estimated)
  4. Study completion30 Jul 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
30 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07552064
Sponsor's protocol ID
O6U.PT. REC/025/002017
Status last verified
Apr 2026
First submitted
20 Apr 2026
Last updated
30 Apr 2026
Results posted
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

A study testing lumbar spine correction training and conventional treatment in people with Low Back Pain, run by October 6 University.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 30 Apr 2026. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

postural habits and awareness scale (PHAS) (time frame: four weeks). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Apr 2026.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in