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Clinical Trial Summary

Effects of exercise on the symptoms of premenstrual syndrome and dysmenorrhoea and blood flow of genital tract. Different self-reported questionnaires and vaginal ultrasound flowmetry are used in the prospective observational trial. The study has interventional and control groups. There are changes in premenstrual syndrome complaints and dysmenorrhoea complaints during the study period.The deegre of menstrual pain and self-awareness improve during the period of study. The ultrasound examination shows changes in genital blood flow after exercise.


Clinical Trial Description

Subject of the study: Examination of premenstrual syndrome and dysmenorrhoea treatment results with Aviva exercise intervention. Method of the study: Prospective observational trial with the participation of volunteers. Questionnaires: 1. PRISM calendar: Prospective Record of the Impact and Severity of Menstrual Symptoms (Reid, 1995). The participants have to fill out this every day, 2. The Body Awareness Questionnaire Shields, S. A., Mallory, M.E., & Simon, A. (1989). The Body Awareness Questionnaire: Reliability and validity. Journal of Personality Assessment, 53(4), 802-815 3. Examination to measure the intensity of menstrual pain: Numeric Rating Scale 4. Heart rate monitoring and documentation before and after the exercises; completion of the Borg Scale of Perceived Exertion to measure exercise intensity; 5. Questionnaire of life style 6. Beck depression questionnaire Ultrasound examination: Doing the Aviva exercises, ultrasound measurements are performed in Robert Hospital (Budapest) on the patients participating in the study. The first measurement is performed for each person before starting the exercises. When the first subject has finished the exercise, a control ultrasound measurement will be carried out. In the control group there is also twice ultrasound examination for the individuals. Measured parameters: PI (pulsatility index) of uterine artery transvaginal ultrasound measurement followed by statistical evaluation of the results. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04618172
Study type Interventional
Source University of Pecs
Contact
Status Completed
Phase N/A
Start date March 1, 2019
Completion date June 30, 2020

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