Effects of Core Stability and Pelvic Clock Exercises in Sacroiliac Joint Dysfunction
Recruiting
N/A
Interventional Study
Sacroiliac Joint Dysfunction
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 25 – 35
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 50 (estimated)
- Sponsor
- Riphah International University · Other
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About This Trial
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)…
Trial Locations
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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 t…
Contacts