Clinical trial Recruiting at 1 site Interventional Ages 25 to 35 Women only

Core stability plus pelvic clock exercises for postpartum sacroiliac joint pain

Official title: Combine Effects of Core Stability and Pelvic Clock Exercises on Pain, Disability and Quality of Life in Postpartum Females With Sacroiliac Joint Dysfunction

Run by Riphah International University · NCT07440849 · Data updated 2026-11-12

This test will see if adding pelvic clock exercises to core stability routines reduces pain and disability for first-time mothers with postpartum sacroiliac joint dysfunction more than core stability alone.

Quick facts

Study typeInterventional
Ages25 Years to 35 Years
SexWomen only
Enrollment50 (estimated)
SponsorRiphah International University
Academic / other
Locations1 site (Sargodha, Punjab Province)
StatusRecruiting
StartedDecember 1, 2024
Main results expectedOctober 2026
Study endsOctober 2026
Registry record updatedSeptember 24, 2026
Trial IDNCT07440849 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are first-time mothers after vaginal delivery who have significant sacroiliac joint pain (NPRS > 6) and positive responses to at least three provocation tests, and who can attend in-person sessions.

Probably not a fit

Patients with prior trauma, other musculoskeletal disorders (like coccydynia or impingement), disc bulge/degeneration, or postpartum depression were excluded and are unlikely to benefit from this protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a randomized controlled trial in Sargodha enrolling 50 primiparous women with postpartum sacroiliac joint dysfunction who report pain greater than 6 on the NPRS and have positive provocation tests. Participants are randomly assigned to an experimental group receiving core stability plus pelvic clock exercises with baseline treatment or a control group receiving core stability exercises with baseline treatment. Intervention lasts 8 weeks with three one-hour sessions per week, and outcomes are measured using the Numeric Pain Rating Scale, Oswestry Disability Index, and WHOQOL-BREF. Data will be analyzed using SPSS version 26 to compare pain, disability, and quality-of-life changes between groups.

Why it matters

Potential benefit: If successful, adding pelvic clock exercises could reduce pain and improve function and quality of life for postpartum women with sacroiliac joint dysfunction.

How similar studies have gone: Core stability exercises have shown benefit for sacroiliac-related pain in prior work, but adding pelvic clock exercises is less well-studied and represents a somewhat novel combination.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Vaginal delivery
* Primiparous women
* Pain intensity greater than 6 on the Numerical Pain Rating Scale (NPRS)
* Positive responses to at least three physical provocation tests suggestive of sacroiliac joint dysfunction

Exclusion Criteria:

* Participants were excluded from the study if they had any of the following conditions:
* Previous history of trauma
* Musculoskeletal disorders (e.g., coccydynia, impingement syndrome)
* Postpartum depression
* Disc bulge or degeneration

Where it's running

  • Al-Khidmat Hospital
    Sargodha, Punjab Province, Pakistan
    Recruiting

Study contacts

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.