Abdominopelvic Fascial Release for Post-Cesarean Menstrual Pain and Scar Mobility

Cesarean section is one of the most commonly performed obstetric surgical procedures worldwide. Although it is frequently necessary to improve maternal and neonatal outcomes, postoperative healing may result in scar formation and fascial adhesions that can contribute to persistent menstrual pain, chronic pelvic pain, reduced scar mobility, abdominal tenderness, and impaired physical function. Fascial restrictions may alter tissue mobility and biomechanics, leading to pain and functional limitations.

Abdominopelvic fascial release is a manual therapy technique that applies sustained, low-load pressure to restricted fascial tissues to restore tissue mobility, improve fascial gliding, reduce pain, and enhance tissue function. Previous studies have demonstrated beneficial effects of fascial release on postoperative scar mobility, pain, and functional recovery; however, evidence regarding its effectiveness in women with menstrual pain following cesarean section remains limited.

The purpose of this prospective, randomized controlled trial is to evaluate whether the addition of abdominopelvic fascial release to a standardized stretching exercise program provides greater clinical benefit than a stretching exercise program alone in women with post-cesarean dysmenorrhea. Participants will be randomly assigned to one of two parallel groups and evaluated before and after completion of the intervention period using predefined clinical outcome measures.

The findings of this study are expected to provide evidence regarding the effectiveness of abdominopelvic fascial release as a non-pharmacological physical therapy intervention for reducing menstrual pain and improving scar mobility following cesarean section. The results may support the integration of fascial release techniques into postpartum rehabilitation programs and contribute to evidence-based physical therapy management for women with post-cesarean pain and scar-related dysfunction.

Inclusion criteria

• Females aged 20 to 35 years.
• History of at least one cesarean section.
• Moderate to severe primary or secondary dysmenorrhea following cesarean section.
• Regular menstrual cycles (21-35 days).
• Body mass index (BMI) between 18.5 and 29.9 kg/m².
• At least 6 months post-cesarean section to allow complete scar healing.
• Presence of restricted cesarean scar mobility on clinical examination.
• Willingness to participate and provide written informed consent.

Exclusion criteria

• Pregnancy or planned pregnancy during the study period.
• Previous abdominal or pelvic surgery other than cesarean section.
• Endometriosis, adenomyosis, uterine fibroids requiring treatment, or other diagnosed gynecological disorders associated with pelvic pain.
• Active pelvic inflammatory disease or genitourinary infection.
• Neurological or musculoskeletal disorders affecting pain perception or mobility.
• Systemic inflammatory, autoimmune, or connective tissue diseases.
• Current participation in another physical therapy or manual therapy program targeting the abdomen or pelvis.
• Use of corticosteroid injections or other invasive treatments to the abdominal or pelvic region within the previous 3 months.
• Contraindications to manual therapy.