Effect of Exercise on Primary Dysmenorrhea
Ključne riječi
Sažetak
Opis
Research; planned as randomized controlled. The research is planned to be carried out in a faculty of Nursing, which provides service with 1 department of a university with 38.482 student capacity, continuing education with 15 faculties, 1,600 academic 1.152 administrative staff in the city center of Konya.
The population of the study is all female students who have been studying since 2018-2019 academic year. The population of the study is all female students who have been studying since 2018-2019 academic year.
The sample size of the study will be composed of female students who have the complaint of dysmenorrhea as a result of the pre-test and who agree to participate in the study.
The power analysis was used to determine the number of cases that required pelvic floor exercise and control groups for the study. In the study of Gamit et al., It was accepted that the mean pain decreased from 6.10 (1 ± 35) to 4.6 with a 1.5 decrease. Considering the data losses to be experienced during the study, 30 female patients were planned to be included in each group (Potur and Kömürcü 2014).
Working Group: Before randomization, Dismenorrhea Diagnosis Form will be applied to women students who agree to participate in the study according to the sample selection criteria and general information about the study will be given and their general consent will be obtained for participation in the study. In accordance with the sample size determined by power analysis, random assignment to experimental and control groups will be made. Block randomization system will be used.
Once randomization has occurred, it is not possible to blind the participants or health professionals. However, in the analysis phase of the data, the blind of the statistician and the writing of the report will be made.
Data Collection Technique and Tools Participation Criteria Form (Dysmenorrhea Diagnostic Form), Data Collection Form, Dysmenorrhea Follow-up Form, Visual Analogue Scale (VAS), Health Related Quality of Life Questionnaire (Short Form-36) (SF-36).
Data collection forms were created by the researcher in the light of literature .
Datumi
Posljednja provjera: | 05/31/2020 |
Prvo podneseno: | 01/13/2020 |
Predviđena prijava poslana: | 06/24/2020 |
Prvo objavljeno: | 06/29/2020 |
Posljednje ažuriranje poslano: | 06/24/2020 |
Posljednje ažuriranje objavljeno: | 06/29/2020 |
Stvarni datum početka studija: | 11/14/2018 |
Procijenjeni datum primarnog završetka: | 05/30/2019 |
Procijenjeni datum završetka studije: | 01/29/2021 |
Stanje ili bolest
Intervencija / liječenje
Behavioral: Exercises group
Faza
Grupe ruku
Ruka | Intervencija / liječenje |
---|---|
Experimental: Exercises group intervention group çalışma grubundaki kadın öğrencilere 8 hafta süresince haftada 4 kez 40 dakika boyunca pelvik taban ve core egzersizleri uygulatılacak | Behavioral: Exercises group Effectıveness of the pelvıc base exercıse on the paın and qualıty of lıfe ın dysmenoral youth 40 minutes exercise intervention 4 times a week for 8 weeks |
No Intervention: control group students will be watched without any intervention |
Kriterij prihvatljivosti
Dobni uvjeti za studiranje | 19 Years Do 19 Years |
Spolovi koji ispunjavaju uvjete za studij | Female |
Prihvaća zdrave volontere | Da |
Kriteriji | Inclusion Criteria: - Describe dysmenorrhea pain severity as five and above on the visual comparison scale in the form of diagnosis of dysmenorrhea, - Being single, - Regular menstruation for the last 6 months (every 21-35 days with no intermittent bleeding), - Body Mass Index (BMI) is between 19-29, - 19-25 years of age - Voluntary acceptance of participation in the study Exclusion Criteria: - Having systemic and chronic diseases, - Physical disability, - Professional athlete, - Using hormonal contraception (such as oral contraceptives and injections) and IUD, - Secondary dysmenorrhea pathology (ultrasound examinations will be performed by a gynecologist). |
Ishod
Primarne mjere ishoda
1. Visual Analogue Scale (pain intensity) [8 weeks]
Sekundarne mjere ishoda
1. Quality of Life Questionnaire(short form-36)(SF-36) [8 weeks]