About this trial
Dysmenorrhea affects up to 90% of women of reproductive age and represents a significant public health concern. Beyond prostaglandin-mediated uterine contractions, dysmenorrhea involves central sensitization mechanisms and myofascial components, including abdominal trigger points. Despite growing interest in physiotherapy for chronic pelvic pain, objective data on tissue-level changes induced by manual therapy remain scarce.
This randomized single-blind sham-controlled trial aims to evaluate the effects of abdominal manual mobilization techniques on (1) tissue stiffness measured by shear wave elastography at the uterine cervix and bilateral abdominal regions, and (2) clinical outcomes including pain intensity and quality of life in women with dysmenorrhea, with or without endometriosis.
Participants will be randomly assigned to either a treatment group receiving standardized abdominal manual therapy or a sham group receiving superficial manual contact. Assessments will be conducted over three menstrual cycles using shear wave elastography, the Numeric Rating Scale (NRS), and the SF-36 questionnaire.
Eligibility criteria
Qualifiers
female sex
aged 18 to 50 years
clinical diagnosis of dysmenorrhea (cyclic pelvic pain during menstruation)
Disqualifiers
Pregnancy or breastfeeding
Delivery less than 1 year prior to enrollment
History of abdominal or pelvic surgery within the past 3 months
Diagnosis of fibromyalgia, diabetes, or cancer
Trial design
Treatments tested in this trial
- Abdominal manual mobilization
- Sham manual contact