Sacroiliac Joint Pain Clinical Trial
Official title:
Efficacy of Adding Low Level Laser Therapy to Postural Correction Exercises on Postnatal Sacroiliac Joint Pain
Verified date | July 2023 |
Source | Cairo University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
the purpose of the study will be to to examine the effect of low level laser therapy on pain and function disability in postnatal women with sacroiliac joint pain.
Status | Completed |
Enrollment | 50 |
Est. completion date | July 28, 2022 |
Est. primary completion date | June 30, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 25 Years to 35 Years |
Eligibility | Inclusion Criteria: - Post natal women suffering from sacroiliac joint pain for at least 3 months. - They should have moderate to severe pain in the sacroiliac joint region (visual analogue scale = 4). - They should have positive findings in at least three of five provocation sacroiliac joint tests (i.e., Patrick's sign, Gaenslen test, compression test, thigh thrust test and distraction test). - Their age will range from 25 to 40 years old. - Their Body mass index (BMI) will be ranged from 25 to 30 Kg /m2. - They should not have any musculoskeletal disorders. Exclusion Criteria: - Lumber or hip joint pathology. - Acute pelvic bacterial or viral infections or tumour. - Taking nonsteroidal anti-inflammatory drugs, or hormonal treatments. - Having positive straight leg raising test. |
Country | Name | City | State |
---|---|---|---|
Egypt | Manal Ahmed | Cairo |
Lead Sponsor | Collaborator |
---|---|
Cairo University |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | pain intensity | The pain intensity will be assessed through visual analogue scale (VAS) for both groups before and after the end of treatment program. Each woman will be asked to mark a point on the line between the extremes that related to her pain intensity. | up to 2 months | |
Primary | pain pressure threshold | pressure algometer will be used to assess pain pressure threshold for both groups before and at the end of the study | up to 2 months | |
Secondary | functional disability | oswestery disability index will be used to assess level of functional disability for both groups before and at the end of the study | up to 2 months |
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