NCT07370272

Brief Summary

This study aims to investigate the difference between integrating lumbopelvic cognitive movement control training versus core stabilization exercises to the conventional physiotherapy program on pain, function, lumbopelvic stability, functional load transfer, and postural control in patients suffering from SIJ pain. The main question it aims to answer is: What are the effects of adding lumbopelvic movement control training versus core stabilization exercises to the conventional physiotherapy program in treating patients with SIJ pain? Researchers will compare adding lumbopelvic movement control training versus core stabilization exercises to the conventional physiotherapy program to investigate its effectiveness in treatment of SIJ pain Participants will:

  • Group (A) - Control Group: will receive conventional physiotherapy program (US and MET)
  • Group (B) - Core Stability Exercises Group: will receive conventional US, MET, and core stability ex's
  • Group (C) - Lumbopelvic cognitive movement control training Group: will receive conventional US, MET, and cognitive movement control training.
  • receive the training protocol 3 times a week for 8 weeks according to the set schedules.
  • perform a home exercise program in the same dose of repetitions and time as in the session.
  • be assessed before and after the intervention and training period to address the outcome measures.

Trial Health

63
Monitor

Trial Health Score

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

Enrollment
36

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started Feb 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress53%
Feb 2026Aug 2026

First Submitted

Initial submission to the registry

January 19, 2026

Completed
8 days until next milestone

First Posted

Study publicly available on registry

January 27, 2026

Completed
5 days until next milestone

Study Start

First participant enrolled

February 1, 2026

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Last Updated

January 27, 2026

Status Verified

January 1, 2026

Enrollment Period

5 months

First QC Date

January 19, 2026

Last Update Submit

January 19, 2026

Conditions

Keywords

cognitive movement control trainingcore stability exercisessacroiliac joint pain

Outcome Measures

Primary Outcomes (2)

  • Pain: using Numerical Pain Rating Scale (NPRS)

    The Arabic Numeric Pain Rating Scale (ANPRS) measures pain intensity in Arabic-speaking patients. The patients will be asked to rate their pain on a 10-point pain scale with a 0 score means no pain and 10 score means maximum pain.

    Baseline (pre-treatment) and after 8 weeks (post-treatment)

  • Functional disability: using Oswestry Disability Index (ODI)

    The Arabic ODI is appropriate for use as a patient reported outcome measure with Arabic speaking individuals with low back pain and /or SIJ pain. The patients will be instructed to fill the ODI which is a self-report pencil and paper survey, where subjects indicate how their pain affects their abilities in 10 questions on domains such as pain intensity, personal care, lifting, walking, sitting, standing, sleeping, social life, travel, and sexual life.

    Baseline (pre-treatment) and after 8 weeks (post-treatment)

Secondary Outcomes (3)

  • Lumbopelvic motor control function: by Pressure Biofeedback Unit (PBU)

    Baseline (pre-treatment) and after 8 weeks (post-treatment)

  • Functional Load transfer: by Active straight leg raise test (ASLR)

    Baseline (pre-treatment) and after 8 weeks (post-treatment)

  • Balance and Postural control: by Single leg stance balance test with eyes closed (SLSBT-EC)

    Baseline (pre-treatment) and after 8 weeks (post-treatment)

Study Arms (3)

Group (A): Control Group

ACTIVE COMPARATOR

The subjects will receive therapeutic ultrasound (for 5 mins, intensity of 1W/cm2). In addition, MET will be applied in prone position for anterior and posterior innominate rotation around the pelvis.

Other: The conventional Physiotherpay Program (US & MET)

Group (B): Core Stability Exercises Group

EXPERIMENTAL

In addition to the traditional protocol delivered in group (A) including US and stretching by MET, subjects in this group will perform core stabilization exercises (CSE) to improve the activation and coordination of deep core stabilizers: transversus abdominis, multifidus, and pelvic floor muscles. The core stabilization exercises consist of 5 exercises: pelvic tilt, double knee to chest, bridging, bird-dog, and cat-camel to be performed in the same order.

Other: The conventional Physiotherpay Program (US & MET)Other: Core Stability Exercises (CSE)

Group (C): Lumbopelvic cognitive movement control training Group

EXPERIMENTAL

In addition to the traditional protocol delivered in group (A) including US and stretching by MET, subjects in this group will undergo lumbopelvic cognitive movement control training (CMCT) that requires the lumbopelvic region to be positioned neutrally and the subject will be asked to consciously maintain the desired alignment and keep a pre-determined value of PBU whilst the lower limbs are actively moved to achieve a pre-determined benchmark. This training will be in multi-directions to address the lumbopelvic uncontrolled movements into flexion, extension and rotation as follows: * Into flexion, we will use double bent leg lift exercise. * Into extension, we will use double leg lower exercise and also, double knee bend exercise * Into rotation, we will use single hip extension exercise and also, bent knee fallout exercise

Other: The conventional Physiotherpay Program (US & MET)Other: Lumbopelvic cognitive movement control training (CMCT)

Interventions

The conventional approach includes ultrasound (US) application combined with muscle energy technique (MET) for the lumbopelvic region. The subjects will receive therapeutic ultrasound (for 5 mins, intensity of 1W/cm2). In addition, MET will be applied in prone for anterior and posterior innominate rotation around the pelvis. The subject will then be asked to apply 20% force against that applied by the therapist and hold that contraction for 10 seconds over 5 to 10 repetitions.

Also known as: control group, traditional program
Group (A): Control GroupGroup (B): Core Stability Exercises GroupGroup (C): Lumbopelvic cognitive movement control training Group

In addition to the conventional protocol including US and MET stretching, subjects in this group will perform core stabilization exercises (CSE) to improve the activation and coordination of deep core stabilizers: transversus abdominis, multifidus, and pelvic floor muscles, which are essential for maintaining lumbopelvic stability and neuromuscular control. The core stabilization exercises consist of 5 exercises: pelvic tilt, double knee to chest, bridging, bird-dog, and cat-camel, to be performed in the same order. Also, before each exercise, the physical therapist will give detailed verbal explanation and visual instructions (pictures) regarding the start and end positions. Each exercise will be done for two sets of 10 repetitions, 3 sessions per week (day after day), for 8 weeks.

Group (B): Core Stability Exercises Group

In addition to the traditional protocol including US and MET stretching, subjects in this group will undergo lumbopelvic cognitive movement control training (CMCT) that requires the lumbopelvic region to be positioned in a neutral alignment and the subject will be asked to consciously maintain the desired alignment and keep a pre-determined value of PBU whilst the lower limbs are actively moved to achieve a pre-determined benchmark. This training will be in multi-directions to address the lumbopelvic uncontrolled movements into flexion, extension and rotation as follows: * Into flexion, we will use double bent leg lift exercise * Into extension, we will use double leg lower exercise and also, double knee bend exercise * Into rotation, we will use single hip extension exercise and also, bent knee fallout exercise Each exercise will be done for 20-30 slow repetitions or up to two consecutive mins. of slow repetitions, with hold time (no pressure change) for at least 5 seconds inbetween.

Group (C): Lumbopelvic cognitive movement control training Group

Eligibility Criteria

Age18 Years - 45 Years
Sexall(Gender-based eligibility)
Healthy VolunteersNo
Age GroupsAdult (18-64)

You may qualify if:

  • Age of the subjects will range between 18 - 45 years for young middle-aged adults.
  • Unilateral SIJ pain lasting for at least 3 months, in lower back, buttock, groin, posterior superior iliac spine (PSIS) and with or without referral pain to the lower extremities.
  • SIJ pain below L5 region.
  • Non-centralized LBP i.e. has no directional preference.
  • Score positive on 3 out of 5 SIJP provocation tests: compression, distraction, sacral thrust, thigh thrust, Gaenslen's.

You may not qualify if:

  • Limb-length discrepancy,
  • Clear signs of nerve root compression (radiating pain, motor and/or sensory deficits,
  • Previous major back surgery or injury, fracture or arthritis of spine, pelvis, hip, knee or ankle joint,
  • Seronegative spondyloarthropathies,
  • Visual or vestibular deficit,
  • Unable to follow command/ cognitive deficits,
  • Postpartum women less than six months,

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Physical Therapy, Cairo University

Giza, Egypt

Location

Related Publications (38)

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MeSH Terms

Interventions

Control Groups

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

Study Officials

  • Salwa F Abdelmajeed, Professor, PT. PhD.

    Cairo University

    STUDY CHAIR
  • Marihan Z Aziz, Lecturer, PT. PhD

    Cairo University

    STUDY DIRECTOR
  • Ihab M Emran, Assistant Professor, MD. PhD

    Faculty of Medicine (Kasr Al-Aini), Cairo University

    STUDY CHAIR

Central Study Contacts

Mina M Morkos, Assistant Lecturer, PT. MSc.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Lecturer of Physical Therapy for Musculoskeletal Disorders and its Surgeries

Study Record Dates

First Submitted

January 19, 2026

First Posted

January 27, 2026

Study Start

February 1, 2026

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

August 1, 2026

Last Updated

January 27, 2026

Record last verified: 2026-01

Locations