Effects of Exercise on the Symptoms of Premenstrual Syndrome and Dysmenorrhoea and Blood Flow of Genital Tract

Premenstrual Syndrome Clinical Trial

Official title:

Effects of Exercise on the Symptoms of Premenstrual Syndrome and Dysmenorrhoea and Blood Flow of Genital Tract

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04618172
• Other study ID #: DRKZ01
• Status: Completed
• Phase: N/A
• Start date: March 1, 2019
• Est. completion date: June 30, 2020

Study information

• Verified date: November 2023
• Source: University of Pecs
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 113
• Est. completion date: June 30, 2020
• Est. primary completion date: June 30, 2020
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 44 Years

Eligibility

Inclusion Criteria:

• BMI 17-35
• regular menstrual cycles (cycles of 21-35 days)
• no endocrinological disease
• no endometriosis
• no experience in Aviva aerob exercises
• symptoms of premenstrual syndrome
• symptoms of dysmenorrhoea
• Score below 40 from Beck depression questionnaire

Exclusion Criteria:

• pregnancy
• pelvic inflamatory disease (PID), secondary dysmenorrhoea
• gynecological operation
• failure to complete the questionnaire (3 consecutive days and 5 days interrupted)
• dissatisfaction with the continuation of the research
• the incidence of adverse life events in the last 3 months
• use of medication (e.g. oral birth control pill,painkiller,antipsychotic tablets)
• participation in other sports programs
• congenital uterine anomalies
• any chronic disease (e.g. neurological, psychological disorders, endocrinological diseases)

Related Conditions & MeSH terms

• Dysmenorrhea
• Dysmenorrhoea
• Premenstrual Syndrome
• Syndrome

Intervention

Other:
• Exercise
30 minute long exercises twice a week

Locations

Country	Name	City	State
Hungary	Róbert Kórház	Budapest

Sponsors (1)

Lead Sponsor	Collaborator
Kovács Zoltán

Country where clinical trial is conducted

Hungary, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change of premenstrual syndrome complaints	Rate of variation of premenstrual syndrome complaints of the participants presented in PRISM (Prospective Record of the Impact and Severity of Menstrual Symptoms) questionnaire	Change of from baseline premenstrual syndrome complaints at next cycle
Primary	Change of dysmenorrhoea complaints	Rate of variation of dysmenorrhoea complaints of the participants presented in Numeric Rating Scale	Change of from baseline dysmenorrhoea complaints at next cycle
Primary	Change in the genital blood flow	PI values of ultrasound flowmetry of uterine arteries presented in charts	Change of from baseline art.uterina ultrasound flowmetry results after aerobic exercises and 30 minute long waiting time for control individuals
Secondary	Change of body-mind awareness	Change of body-mind awareness using The Body Awareness Questionnaire	Change of from baseline body-mind awareness results at the end of the first and second cycle
Secondary	Adherence	Measurement of adherence: frequency of visiting exercising group	up to 2 menstrual cycle