RecruitingNot Applicable

Effectiveness of Combined Kinesiotapping and Core Stability Exercises in SIJ Dysfunction

Pakistan44 participantsStarted 2026-03-26

Plain-language summary

The aim of this randomized controlled trial is to determine the combined effects of kinesiotaping and core stability exercises on pain, functional disability, and fear-avoidance beliefs in female patients with sacroiliac joint dysfunction.

Who can participate

Age range

20 Years – 50 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Bilateral SIJ pain for \>3 months * Pain intensity ≥4 on NPRS * ≥3 positive SIJ provocation tests (Laslett Cluster) * Willing to participate in 6-week intervention program Exclusion Criteria: * Low back pain of other origin * Pregnancy * Recent spinal surgery * Inflammatory joint diseases (AS, RA) * Previous physiotherapy or kinesiotaping for SIJD in past 3 months * Known allergies to kinesiotape or skin conditions * History of fractures or trauma

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Numeric Pain Rating Scale (NPRS)

Timeframe: 6th week.

Modified Oswestry Disability Index (MODI)

Timeframe: 6 weeks

Fear-Avoidance Beliefs Questionnaire (FABQ)

Timeframe: 6 weeks

Trial details

NCT IDNCT07484503

SponsorRiphah International University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-06

Contact for this trial

maria Khalid, MSOMPT

03315369768 maria.khalid@riphah.edu.pk

View on ClinicalTrials.gov More Sacroiliac Dysfunction trials