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 @ 3:53 PM
Ignite Modification Date:
2025-12-24 @ 3:53 PM
NCT ID:
NCT07130292
Eligibility Criteria:
Inclusion Criteria:
* Female participants aged 18-25 years
* Regular menstrual cycles
* Diagnosed with primary dysmenorrhea (no secondary dysmenorrhea or other gynecological disorders)
* Menstrual pain intensity ≥ 4 on the Visual Analog Scale (VAS) during the menstrual cycle
* Willingness to participate and ability to provide informed consent
Exclusion Criteria:
* Diagnosis of secondary dysmenorrhea or other gynecological disorders (e.g., endometriosis, adenomyosis, uterine fibroids)
* Current pregnancy or breastfeeding
* History of abdominal or pelvic surgery in the past 6 months
* Current use of hormonal therapy or analgesic medication that could affect menstrual pain assessment
* Participation in regular abdominal or core strengthening exercise programs within the last 3 months
* Any musculoskeletal, neurological, or systemic condition that could interfere with exercise performance or study participation
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
25 Years
Study:
NCT07130292
Study Brief:
Protocol Section:
NCT07130292