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临床试验/NCT07717983
NCT07717983尚未招募不适用

Abdominopelvic Fascial Release for Post-Cesarean Menstrual Pain and Scar Mobility: A Randomized Controlled Trial

Cairo University0 个研究点目标入组 58 人开始时间: 2026年7月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
入组人数
58
主要终点
Change in Menstrual Pain Intensity

研究概览

简要总结

The goal of this randomized controlled clinical trial is to determine whether adding abdominopelvic fascial release to a standardized stretching exercise program is more effective than stretching exercises alone in reducing menstrual pain in women following cesarean section. The study will enroll women aged 20 to 35 years with moderate to severe dysmenorrhea after cesarean delivery. Researchers will compare the effects of abdominopelvic fascial release combined with stretching exercises with stretching exercises alone on menstrual pain and scar mobility. Participants will be randomly assigned to one of two treatment groups, undergo assessments before and after the intervention period, and receive the assigned treatment according to the study protocol.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

Outcome assessments will be performed by an independent assessor who will be blinded to treatment allocation. Participants will be instructed not to disclose their assigned intervention to the assessor. Due to the nature of the interventions, participants and treating therapists cannot be blinded.

入排标准

年龄范围
20 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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.

研究组 & 干预措施

Abdominopelvic Fascial Release + Stretching Exercises

Experimental

Participants assigned to the experimental group will receive abdominopelvic fascial release in combination with a standardized stretching exercise program. Abdominopelvic fascial release will be administered for 30 minutes per session, twice weekly for 2 weeks, and the stretching exercise program will be provided for 45 minutes per session, three sessions per week for 4 weeks.

干预措施: Abdominopelvic fascial Release (Other)

Stretching Exercises Alone

Active Comparator

Participants assigned to the control group will receive a standardized stretching exercise program for 45 minutes per session, three sessions per week for 4 weeks.

干预措施: Abdominopelvic fascial Release (Other)

结局指标

主要结局

Change in Menstrual Pain Intensity

时间窗: Baseline and immediately after completion of the 4-week intervention period.

Menstrual pain intensity will be assessed using the Visual Analog Scale (VAS), a validated 10-cm scale ranging from 0 (no pain) to 10 (worst imaginable pain). The primary outcome is the change in VAS score from baseline to the end of the intervention period.

次要结局

  • Change in Cesarean Scar Mobility(Baseline and immediately after completion of the 4-week intervention period.)
  • Change in Pressure Pain Threshold(Baseline and immediately after completion of the 4-week intervention period.)
  • Change in Dysmenorrhea Severity(Baseline and immediately after completion of the 4-week intervention period.)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Amira Ibrahim Hassanein Abdel-aal

Lecturer of Physical Therapy for Women's Health

Horus University

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