Efficacy of Adding LLL Therapy to Postural Correction Exercises on Postnatal SIJ Pain

Cairo University (CU)

Status: Completed

Conditions: Sacroiliac Joint Pain

Treatments: Other: LLL therapy , postural correction ex

Study type: Interventional

Funder types: Other

Identifiers

NCT05306236

P.T.REC/012/003492

Details and patient eligibility

About

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.

Full description

Women are more susceptible to sacroiliac joint pain than men because the physiological changes associated with childbearing (e.g. pregnancy associated with weight gain, exaggerated lumber lordosis, hormone-induced ligamentous laxity and the mechanical trauma associated with childbirth) may result in sacroiliac joint pathology .

Low level laser is effective for treatment of various musculoskeletal pain disorders. It releases local neurotransmitters such as serotonin and endorphins. Additionally, the analgesic effect of LLLT is thought to be related to its anti-inflammatory action. Laser irradiations also relieve pain by alleviating and removing swelling and by increasing oxygenation of the tissues, thus results in reduction of the pain .

Enrollment: 50 patients

Sex: Female

Ages: 25 to 35 years old

Volunteers: Accepts Healthy Volunteers

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.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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50 participants in 2 patient groups

LLL therapy and postural correction ex (study group)

Experimental group

Description:

study group will be treated by low level laser therapy and postural correction exercises

Treatment:

Other: LLL therapy , postural correction ex

postural correction ex (control group)

Experimental group

Description:

control group will be treated by postural correction exercises only

Treatment:

Other: LLL therapy , postural correction ex