Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 5:25 PM
Ignite Modification Date:
2025-12-24 @ 5:25 PM
NCT ID:
NCT07196150
Eligibility Criteria:
Inclusion Criteria:
* Female, aged 18-25 years
* Gynecological examination and ultrasound confirming absence of pelvic pathology
* History of primary dysmenorrhea for at least 6 months, with pain intensity ≥4 on the Numeric Rating Scale (0-10) during the first 3 days of menstruation
* Regular menstrual cycles (21-35 days)
* Nulliparous (no history of pregnancy or childbirth)
* No systemic, metabolic, rheumatologic, or lumbar pathology
* Willingness to participate in the 8-week intervention program and attend follow-up assessments
Exclusion Criteria:
* Diagnosis of secondary dysmenorrhea (e.g., endometriosis, pelvic inflammatory disease, uterine fibroids, ovarian cysts)
* Current pregnancy or planning to become pregnant during the study period
* History of pelvic or abdominal surgery
* History of sexually transmitted diseases
* Current use of antidepressants, anxiolytics, or hormonal therapy (e.g., oral contraceptives, intrauterine device)
* Known neurological, psychiatric, or systemic musculoskeletal disorders
* Cognitive impairment or attention deficit that may interfere with participation
* Participation in regular exercise in the last 6 months
* Use of alternative therapies for dysmenorrhea (e.g., acupuncture, massage)
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
25 Years
Study:
NCT07196150
Study Brief:
Protocol Section:
NCT07196150