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 @ 11:29 PM
Ignite Modification Date:
2025-12-24 @ 11:29 PM
NCT ID:
NCT06860256
Eligibility Criteria:
Inclusion Criteria:
* Nulliparous female university students aged 18-25 years who volunteered to participate in the study, met the criteria specified in the PD Consensus Guidelines and were diagnosed with PD by a gynecologist
* Individuals with a body mass index (BMI) between 18-35
* Individuals with a regular menstrual cycle (28 ± 7 days)
* Individuals with menstrual pain Visual Analog Scale (VAS) score of 4 cm or higher for the last 6 months
Exclusion Criteria:
* Gastrointestinal, urogynecologic, autoimmune, psychiatric, neurological diseases or other chronic pain syndromes
* Having given birth and/or being pregnant
* Intrauterine device users
* Pelvic surgery patients
* Taking oral contraceptives or medication, including antidepressants, for at least 6 months before the study
* Those with a pathological history or ultrasonography result indicating secondary dysmenorrhea
* Those who use alternative treatment methods and exercise regularly
* Serious traumatic life events that occurred in the three months prior to the start of the study
* Communication problems that may interfere with the implementation of assessments and/or treatment program
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
25 Years
Study:
NCT06860256
Study Brief:
Protocol Section:
NCT06860256