Effects of Core Stability and Pelvic Clock Exercises in Sacroiliac Joint Dysfunction
Combine Effects of Core Stability and Pelvic Clock Exercises on Pain, Disability and Quality of Life in Postpartum Females With Sacroiliac Joint Dysfunction
- Sacroiliac Joint Dysfunction
At a glance
- Phase
- Phase not stated
- Study type
- Interventional
- Sponsor
- Riphah International University
- Enrolment target
- 50
- Started
- 1 December 2024
- Main results due
- October 2026
- Study sites
- 1
- Registry updated
- 24 September 2026
Can you take part?
- Ages 25 years to 35 years.
- Women only.
- Healthy volunteers can take part.
These are the headline rules only. Every study has a longer list, and whether you are eligible is decided by the research team at the site — never by this page.
Read the full eligibility 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
What this study is about
In the sponsor’s own words, from the registry.
The study will be a randomized control trial and will be conducted in DHQ and Sadiq Hospital in Sargodha District. This study will be completed in time duration of 10 months after the approval of synopsis. Nonprobability convenience sampling technique will be used and 50 participants will be recruited in study after randomization. The subjects will be divided into two groups. Group A(Experimental) will receive core stability and pelvic clock exercises with baseline treatment while Group B(Control) will receive only core stability exercises after baseline treatment. The tools that will be used are Numeric Pain Rating Scale (NPRS), Oswestry Disability index (ODI) and WHOQOL-BREF. Treatment have duration of 8 weeks with 3 sessions per week and an hour per session is requires. After data collection, data will be analyzed by using SPSS version 26.
Study sites(1)
Al-Khidmat Hospital
Sargodha, Punjab Province, Pakistan
Recruiting
Showing 1 of 1 sites. 1 of the 1 site on this study is recruiting right now — a site can stop enrolling while the study as a whole is still open.
Source: ClinicalTrials.gov record NCT07440849. Trialion does not run this study, is not paid to refer anyone to it, and cannot enrol you. Eligibility is always decided by the research team at the site.
Not the right study?
Answer three questions and see the studies recruiting near you, in plain language.
Find a study for me