Assessment of the Impact of Soft Tissue Mobilization on the Scar in Patients After Cesarean Section

Nicolaus Copernicus University

Status: Completed

Conditions: Cesarean Section Complications

Treatments: Other: Manual therapy (myofascial release, soft tissue mobilization)

Study type: Interventional

Funder types: Other

Identifiers

NCT06446258

CMUMKscarmobilisation

Details and patient eligibility

About

The aim of the study is to assess the impact of soft tissue mobilization on the scar in patients after cesarean section. An additional aim is to assess the relationship between the initial stiffness and elasticity of the scar and the age of the patients, the number of cesarean sections performed, as well as the time that has passed since the last cesarean section. Two physiotherapeutic interventions will be performed in the form of mobilization of the soft tissues (myofascial release techniques) of the lower abdominal area and the cesarean section scar, two weeks apart. The researchers will perform an assessment before and after each therapeutic session, as well as 2 weeks after the last therapy (follow-up). The level of satisfaction with life (Satisfaction with Life Scale (SWLS)) as well as the area of the cesarean section scar (Vancouver Scar Scale (VSS), scar assessment according to the Mustoe classification) will be analyzed. Researchers will also assess the sequence of abdominal muscle contractions during activation of the pelvic floor muscles (ultrasound examination) and quantify the state of soft tissue tension using the MyotonPro measuring device.

Enrollment: 30 patients

Sex: Female

Ages: 18 to 45 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• women aged 18-45,
• undergone at least 1 cesarean section in a period of not less than 6 months,
• not using physiotherapy for a cesarean section scar

Exclusion criteria

• women under 18 and over 45,
• pregnant women,
• presence of abdominal mesh,
• condition after abdominoplasty; nephrectomy; hysterectomy; cystectomy,
• uterine fibroids,
• stoma,
• occurrence of neurological symptoms (exclusion based on a functional test including the following elements: trunk flexion test in a sitting position (Slump test), Babinski test and clonic reflex test, tension tests for the sciatic nerve (passive straight leg raise test) and bowstring test and femoral nerve test (in lying on the front and on the side), examination of knee and ankle reflexes, as well as assessment of superficial sensation and strength of indicator muscles in the innervation of the lumbar-sacral spine),
• positive result of pain provocation tests: axial compression of the spine and maximum compression of the intervertebral foramen in the lumbosacral spine area,
• presence of contraindications to myofascial release therapy (active cancer, deep vein thrombosis, aneurysms, infectious diseases, viral and bacterial infections, acute inflammation and fever),
• women who underwent CC surgery in less than 6 months,
• previous surgical treatment and spine injury,
• vertical scar after cesarean section,
• use of physiotherapy treatments in the last six months,
• additionally the following comorbid conditions: cancer, diabetes, osteoporosis, diseases of the digestive system, circulatory system, rheumatic, mental and gynecological diseases, pregnancy

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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30 participants in 1 patient group

Experimental Group

Experimental group

Description:

Two manual therapy treatments (myofascial release, soft tissue mobilization) in the lower abdominal area and the cesarean section scar, two weeks apart.

Treatment:

Other: Manual therapy (myofascial release, soft tissue mobilization)