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Shock Wave and Core Exercises for Postpartum Sacroiliac Pain

Effect of Adding Shock Wave Therapy to Core Stability Exercises in Treatment of Postpartum Sacroiliac Joint Pain: A Single-blinded, Randomized Controlled Trial.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06124365
Enrollment
40
Registered
2023-11-09
Start date
2023-11-10
Completion date
2024-01-25
Last updated
2023-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum Sacroiliac Joint Pain

Brief summary

Despite the high popularity and novelty of shock wave therapy (SWT), it is surprising that just one study has examined the effect of SWT on patients with SIJD and their functional ability following treatment by using subjective assessment tools like numeric rating scale (NRS) and limited by its small sample size and lack of long-term follow-up. Therefore, the present study is expected to contribute to the body of knowledge by exploring the effect of adding SWT to core stability exercises in the management of postpartum sacroiliac joint pain.

Interventions

OTHERShock wave therapy and core stability exercises

20 post-partum women with SIJP will be treated by ESWT once weekly combined with core stability exercises 3 times per week for 6 weeks.

OTHERcore stability exercises only

20 post-partum women with SIJP will be treated by core stability exercises 3 times per week for 6 weeks.

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
25 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* post-partum women diagnosed with SIJP with limitation of its movement referred from the orthopedist. * Age is between 25-35 years old. * Their body mass index will be ranged from 25-35 kg/m2.

Exclusion criteria

Patients who have one of the following criteria will be excluded from the study: * Previous spinal surgery. * Medical diagnosis other than SIJ dysfunction. * Patients who had any other spine disorders. * Patients who had leg length discrepancies. * Patients with congenital postural deformities. * Patients with spinal cord injury or acute or unstable neurological signs. * Patients with cauda equina symptoms related to the spine including changes in bowel or bladder control and perineal sensation. * Patients with lumber intervertebral disc, spondylosis, lumbar canal stenosis and spondylolysthesis.

Design outcomes

Primary

MeasureTime frameDescription
Sacroiliac joint pain intensitychange from base line at 6 weeks.Sacroiliac joint pain intensity will be measured by visual analogue scale
pain pressure thresholdchange from base line at 6 weeks.pain pressure threshold will be measured by pressure algometer
functional disabilitychange from base line at 6 weeksfunctional disability will be measured by Oswestry disability index

Secondary

MeasureTime frameDescription
quality of lifechange from base line at 6 weeks.quality of life will be measured by the standard quality of life assessment tool which is known as the short-form SF 36 tool

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026