Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT05428813 |
Other study ID # |
E-41997688-050.99-40210 |
Secondary ID |
|
Status |
Completed |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
April 15, 2022 |
Est. completion date |
December 30, 2022 |
Study information
Verified date |
February 2023 |
Source |
Kutahya Health Sciences University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
This study will be conducted to determine the effect of art therapy techniques on
premenstrual syndrome symptoms.The study is a randomized controlled type study. The study
will be conducted with 70 female students with premenstrual syndrome. In the study, which
consists of two groups, experimental (n=35) and control (n=35), art therapy techniques will
be applied to the students in the experimental group for 8 weeks. The control group will
continue their routine coping habits. Both groups will be evaluated with the Premenstrual
Syndrome scale at the end of the study, and the difference between the groups will be
examined.
Description:
First of all, ethics committee approval will be obtained by applying to the
Non-Interventional Ethics Committee of the Rectorate of Kütahya Health Sciences University
for the research. Then, written permission will be obtained from the Dean of the Faculty of
Health Sciences of Kütahya Health Sciences University and the Department of Midwifery. In
addition, written consent was obtained for the PMSS to be used in the research. At the first
stage, the researcher will apply the research forms to all midwifery students willing to
participate in the study without using any sampling method. The forms will be applied to
volunteer and willing students after the lesson, in an appropriate classroom, by explaining
the research and purpose. It is anticipated that the filling time of the forms will be 15-20
minutes on average. Then, all data will be evaluated in the SPSS program and randomization
will be provided among the students who meet the inclusion criteria. Participants will be
evaluated in two groups. One of the groups is the study group, where artistic techniques will
be applied, and the other group is the control group, which will continue their routine
coping habits for PMS. Participants will be randomly assigned to one of two groups using the
www.randomizer.org program. Students in the study group (35) will do group work that will
last for 30-35 minutes, one day a week, for 8 weeks, with the Artistic Techniques Education
Directive prepared by the researcher holding a certificate on artistic techniques in parallel
with the education they received. There is no intervention or therapy involved here. Art is
used as an expressive technique, and these techniques enable students to better understand
and interpret their own emotions at the end of their activity. The researcher will only apply
the techniques and pose non-directive questions. At the same time, these techniques raise
awareness. At the end of 8 weeks, students will be reassessed with PMSS. Students in the
control group (35) will not be subjected to any application, and in parallel with the study
group, they will be told to continue their routine habits regarding PMS. At the end of 8
weeks, students will be reassessed with PMSS.