Sacroiliac Joint DysfunctionNCT07716215
Comparison of Core Stability and Hip Strengthening Protocols in Sacroiliac Joint Dysfunction
A study testing Core Stabilization and Hip Strengthening Exercises in people with Sacroiliac Joint Dysfunction, run by Riphah International University at 1 site in Pakistan.
Trial summary
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. Read more about this study
- Who is it for?
- Ages 25 to 55 years
- Conditions the study is for
- Sacroiliac Joint Dysfunction
- What is being tested?
- Core Stabilization and Hip Strengthening Exercises
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 22 participants
- Where
- 1 sitePakistan
- Study dates
- 30 Jun 2026to 15 Nov 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 55 years
- All sexes
- No healthy volunteers
- Adult
Who may be able to join
- 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.
Who cannot join
- 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.
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Pakistan1 site, 1 recruiting
- Recruiting
National physiotherapy center
Rawalpindi
Muhammad Abdullah, PT, 03313134355, npcr.pak@gmail.com
About this study
Official title: 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.
Read the 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.
- Conditions
- Sacroiliac Joint Dysfunction
- Being tested
- Core Stabilization, Hip Strengthening Exercises
- Keywords
- Sacroiliac Joint Dysfunction, Core Stability Exercises, Hip Strengthening Exercises, Low Back Pain, Oswestry Disability Index, Numeric Pain Rating Scale
- 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.
Core StabilizationOther
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.
Hip Strengthening ExercisesOther
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.
| Study group | Role | What they receive |
|---|---|---|
| Core Stabilization Exercises | Experimental | Participants in this group will receive core stabilization exercises Receives: Other: Core Stabilization |
| Hip Strengthening Exercises | Active comparator | Participants in this group will receive hip strengthening exercises Receives: Other: Hip Strengthening Exercises |
What is being measured
The primary outcome is the main question the study is designed to answer.
Balance (Gait and Balance App)
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.
Measured: 4 weeks
Proprioception (Joint Repositioning Error Test)
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.
Measured: 4 weeks
Posture Assessment (Flexicurve Ruler)
Changes from baseline posture will be assessed using the Flexicurve ruler to measure lumbar curvature and spinal alignment associated with sacroiliac joint dysfunction.
Measured: 4 weeks
Secondary outcomes (3)
Numeric Pain Rating Scale (NPRS)
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.
Measured: 4 weeks
Oswestry Disability Index (ODI)
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.
Measured: 4 weeks
Pelvic Alignment (Pelvic Inclinometer)
Changes from baseline pelvic alignment will be measured using a pelvic inclinometer to assess pelvic tilt and asymmetry related to sacroiliac joint dysfunction.
Measured: 4 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Jul 2026
- Study start30 Jun 2026
- Primary completion30 Oct 2026 (estimated)
- Study completion15 Nov 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Sacroiliac Joint DysfunctionStudies of the same condition, open and under way.
- More trials run by Riphah International UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- 22 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Riphah International University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Muhammad Affan Iqbal, PhD*, Principal investigator, Riphah International UniversitySaba Naz, MSPT*, Principal investigator, Riphah International University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07716215
- Sponsor's protocol ID
- RIPHAH/RCRAHS/REC/02287
- Status last verified
- Jul 2026
- First submitted
- 16 Jul 2026
- Last updated
- 21 Jul 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 21 Jul 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Comparison of Core Stability and Hip Strengthening Protocols in Sacroiliac Joint Dysfunction.
- ClinicalTrials.gov ID
- NCT07716215
- Acronym / sponsor ID
- RIPHAH/RCRAHS/REC/02287
- Conditions
- Sacroiliac Joint Dysfunction
- Keywords
- Sacroiliac Joint Dysfunction, Core Stability Exercises, Hip Strengthening Exercises, Low Back Pain, Oswestry Disability Index, Numeric Pain Rating Scale
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 22 participants (estimated)
- Lead sponsor
- Riphah International UniversityUniversity, hospital or other
- Study start
- 30 Jun 2026 (actual)
- Primary completion
- 30 Oct 2026 (estimated)
- Study completion
- 15 Nov 2026 (estimated)
- First posted
- 21 Jul 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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 design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Core Stabilization Exercises | Experimental | Other: Core StabilizationParticipants in this group will receive core stabilization exercises |
| Hip Strengthening Exercises | Active comparator | Other: Hip Strengthening ExercisesParticipants in this group will receive hip strengthening exercises |
Who may qualify
- Ages
- 25 to 55 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult
Key inclusion criteria (5 listed)
- 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.
Key exclusion criteria (6 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Core StabilizationEach 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. | Other | Core Stabilization Exercises |
| Hip Strengthening ExercisesExercises 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. | Other | Hip Strengthening Exercises |
Primary outcome
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.
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.
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.
3 secondary outcomes
Numeric Pain Rating Scale (NPRS)
Time frame: 4 weeks
Oswestry Disability Index (ODI)
Time frame: 4 weeks
Pelvic Alignment (Pelvic Inclinometer)
Time frame: 4 weeks
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Jul 2026.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Muhammad Affan Iqbal, PhD* principal investigator
Riphah International University
Saba Naz, MSPT* principal investigator
Riphah International University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Core Stabilization and Hip Strengthening Exercises in people with Sacroiliac Joint Dysfunction, run by Riphah International University at 1 site in Pakistan.
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 5 inclusion and 6 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: looking for participants now, as of the sponsor's last update on 21 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.
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?
Contact Imran Amjad, PhD (03324390125, Imran.amjad@riphah.edu.pk), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Balance (Gait and Balance App) (time frame: 4 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 21 Jul 2026.