Comparison of Core Stability and Hip Strengthening Protocols in Sacroiliac Joint Dysfunction

July 16, 2026 updated by: Riphah International University

Comparison of Core Stability and Hip Strengthening Protocols in Sacroiliac Joint Dysfunction.

The aim of this research is to compare the effects of core stability exercises and hip strengthening exercises on pain, posture, balance, proprioception, and functional status in patients with sacroiliac joint dysfunction. A randomized controlled trial will be conducted at Benazir Bhutto Hospital. The sample size will be 22 participants. The subjects will be divided into two groups, 11 subjects in the core stability exercise group and 11 subjects in the hip strengthening exercise group. The study duration will be 6 months. The sampling technique applied will be non-probability purposive sampling. Only 25-55 years individuals with unilateral sacroiliac joint dysfunction for more than 3 months and NPRS score ≥5 will be included. Tools used in the study are Numeric Pain Rating Scale (NPRS), Oswestry Disability Index (ODI), Pelvic Inclinometer, Flexicurve Ruler, Gait and Balance App, and Joint Repositioning Error test. Data will be analyzed through SPSS version 25.

Study Overview

Detailed Description

Sacroiliac joint dysfunction is an important cause of low back pain and functional disability in many individuals. The sacroiliac joint is a synovial joint located between the sacrum and the ilium of the pelvis and plays a critical role in transferring loads between the upper body and lower extremities. When abnormal motion, inflammation, or misalignment occurs in this joint, it leads to pain and dysfunction. Patients with SIJ dysfunction commonly experience pain in the lower back, buttocks, posterior thigh, and sometimes radiating pain toward the lower limb.

The sacroiliac joint is supported by strong ligaments such as the interosseous sacroiliac ligament, anterior sacroiliac ligament, posterior sacroiliac ligament, sacrotuberous ligament, and sacrospinous ligament. These structures provide stability and restrict excessive motion of the joint. However, trauma, pregnancy, repetitive stress, degenerative changes, or previous lumbar fusion surgery can disturb the normal biomechanics of the joint and lead to sacroiliac joint dysfunction. Because symptoms of sacroiliac joint dysfunction often mimic other causes of low back pain such as facet joint syndrome or lumbar disc pathology, it can be difficult to diagnose clinically.

Patients with sacroiliac dysfunction often present with pain below the L5 level, difficulty in prolonged sitting, walking, climbing stairs, or lying on the affected side. Pain is usually localized around the posterior superior iliac spine. Diagnosis is typically based on clinical examination and provocation tests such as thigh thrust test, sacral thrust test, compression test, distraction test, Gaenslen's test, and flexion, abduction and external rotation test. A combination of these tests increases diagnostic accuracy.

Physiotherapy plays a major role in the management of sacroiliac joint dysfunction. Conservative treatment approaches focus on reducing pain, improving stability of the lumbopelvic region, and restoring normal functional movement patterns. Among these interventions, core stabilization exercises and hip strengthening exercises are commonly used. Core stabilization exercises focus on strengthening deep trunk muscles such as transversus abdominis, multifidus, pelvic floor muscles, and diaphragm, which improve spinal stability and control of the lumbopelvic region. Improved core stability reduces excessive shear forces across the sacroiliac joint and helps maintain proper pelvic alignment.

Hip strengthening exercises, on the other hand, primarily target muscles such as the gluteus medius, gluteus maximus, and hip external rotators. Weakness of these muscles can result in poor pelvic stability and altered load transfer during functional activities such as walking, standing, and lifting. Strengthening these muscles improves pelvic control, enhances force distribution across the lumbopelvic region, and reduces stress on the sacroiliac joint.

Previous studies have reported beneficial effects of both core stabilization and hip strengthening exercises in patients with low back pain and sacroiliac joint dysfunction. Research suggests that core stabilization exercises can improve proprioception, balance, neuromuscular control, and functional ability, while hip strengthening exercises improve gluteal activation, pelvic stability, and gait mechanics. However, limited research directly compares the effectiveness of these two exercise protocols in patients with unilateral sacroiliac joint dysfunction.

Therefore, the purpose of this study is to compare the effects of core stabilization exercises and hip strengthening exercises on pain, posture, balance, proprioception, and functional status in patients with sacroiliac joint dysfunction. It is hypothesized that there will be a significant difference between the effects of core stabilization exercises and hip strengthening exercises in improving clinical outcomes in patients with sacroiliac joint dysfunction.

Study Type

Interventional

Enrollment (Estimated)

22

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

      • Rawalpindi, Pakistan
        • Recruiting
        • National physiotherapy center
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Patients aged 25-55 years diagnosed with unilateral sacroiliac joint dysfunction.
  • Patients having pain in the sacroiliac region for more than 3 months.
  • Numeric Pain Rating Scale (NPRS) score ≥ 5.
  • Patients with positive sacroiliac joint provocation tests (such as FABER test, compression test, distraction test, thigh thrust test, or sacral thrust test).
  • Individuals able to participate in exercise therapy and follow treatment instructions.

Exclusion Criteria:

  • History of lumbar spine surgery or pelvic surgery.
  • Lumbar disc herniation or severe spinal pathology.
  • Inflammatory joint diseases such as rheumatoid arthritis or ankylosing spondylitis.
  • Neurological disorders affecting balance or proprioception.
  • Recent fracture or trauma of the spine or pelvis.
  • Pregnancy.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Core Stabilization Exercises
Participants in this group will receive core stabilization exercises
Each session will begin with hot pack application over the sacroiliac region for 10 minutes followed by the exercise protocol and cool-down stretching. Treatment will be provided 3 sessions per week for 4 weeks, with each session lasting approximately 40-45 minutes.
Active Comparator: Hip Strengthening Exercises
Participants in this group will receive hip strengthening exercises
Exercises will be performed with resistance at approximately 75-80% repetition maximum for 2-3 sets of 8-12 repetitions. Each session will start with 10 minutes of hot pack application over the sacroiliac region followed by strengthening exercises and cool-down stretching including hamstring and piriformis stretches. Treatment will be provided 3 sessions per week for 4 weeks, with each session lasting approximately 40-45 minutes.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Balance (Gait and Balance App)
Time Frame: 4 weeks
Changes from baseline balance will be assessed using the Gait and Balance App, which evaluates postural stability and balance performance during functional activities in patients with sacroiliac joint dysfunction. This tool helps identify balance impairments related to lumbopelvic instability.
4 weeks
Proprioception (Joint Repositioning Error Test)
Time Frame: 4 weeks
Changes from baseline proprioception will be measured using the Joint Repositioning Error Test, which evaluates the ability of patients to accurately reposition the lumbopelvic region. It helps assess sensorimotor control deficits associated with sacroiliac joint dysfunction.
4 weeks
Posture Assessment (Flexicurve Ruler)
Time Frame: 4 weeks
Changes from baseline posture will be assessed using the Flexicurve ruler to measure lumbar curvature and spinal alignment associated with sacroiliac joint dysfunction.
4 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Numeric Pain Rating Scale (NPRS)
Time Frame: 4 weeks
Changes from baseline Numeric Pain Rating Scale will be used to assess pain intensity. The scale ranges from 0-10, where 0 indicates no pain and 10 indicates worst possible pain.
4 weeks
Oswestry Disability Index (ODI)
Time Frame: 4 weeks
Changes from baseline Oswestry Disability Index will be used to measure functional disability in patients with sacroiliac joint dysfunction. The ODI consists of 10 sections assessing limitations in daily activities. Higher scores indicate greater disability.
4 weeks
Pelvic Alignment (Pelvic Inclinometer)
Time Frame: 4 weeks
Changes from baseline pelvic alignment will be measured using a pelvic inclinometer to assess pelvic tilt and asymmetry related to sacroiliac joint dysfunction.
4 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Muhammad Affan Iqbal, PhD*, Riphah International University
  • Principal Investigator: Saba Naz, MSPT*, Riphah International University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 30, 2026

Primary Completion (Estimated)

October 30, 2026

Study Completion (Estimated)

November 15, 2026

Study Registration Dates

First Submitted

July 16, 2026

First Submitted That Met QC Criteria

July 16, 2026

First Posted (Actual)

July 21, 2026

Study Record Updates

Last Update Posted (Actual)

July 21, 2026

Last Update Submitted That Met QC Criteria

July 16, 2026

Last Verified

July 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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