Comparison of the Efficacy of Pharmacology and Non-pharmacological Treatment in Women With Primary Dysmenorrhea.

This study aims to determine the effects of different treatment approaches in women diagnosed with primary dysmenorrhea. Patients who are examined by a physician and diagnosed with primary dysmenorrhea using ultrasonography will be included in the study. The cases will be divided into 5 groups by randomization. In the first group, patients who are prescribed diosmin by the attending physician will be taken. The second group; Patients who are prescribed naproxen sodium by the attending physician will be taken. The third group; Pelvic floor exercises will be performed 2 days a week and 12 weeks a week using the motor imagination technique created by the women health physiotherapist. In the fourth group, acupressure technique applied by applying pressure to non-invasive acupuncture points will be applied daily for 12 weeks. The fifth group will be the control group. Online access will be synchronized with the phone or computer, and training sessions will not be recorded to protect the patient's personal information. Cases will be evaluated online at the beginning of the study and at the end of the 12-week program.

Inclusion criteria

• Over the age of 18 whose menstrual cycle continues,
• Primary dysmenorrhea was diagnosed by the obstetrician by ultrasonographic evaluation.
• Participants who agree to participate in the study will be included.
• Participants in the diosmin group who were prescribed diosmin by the physician
• Participants in the NSAI group who were prescribed an NSAI by the physician

Exclusion criteria

• Receiving hormone therapy
• Those receiving psychiatric treatment for stress disorder or anxiety
• Intrauterine contraceptive device
• Using birth control pills
• Women diagnosed with secondary dysmenorrhea
• With neurological deficits
• Patients who were not suitable for NSAI and Diosmin treatment by the physician were excluded by the physician and were not included in our study.