Investigation of the Effects of Training Given to Cope With Premenstrual Syndrome and Mandala Activity on Premenstrual Symptoms

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The research employs a pre-test post-test control group design with a randomized controlled semi-experimental approach to determine the impact of education provided for coping with premenstrual syndrome and Mandala activity on premenstrual symptoms. Research Hypotheses: H01: Mandala activity is not effective in reducing premenstrual symptoms. H02: Education provided for coping with premenstrual syndrome is not effective in reducing premenstrual symptoms. H13: Mandala activity is effective in reducing premenstrual symptoms. H14: Education provided for coping with premenstrual syndrome is effective in reducing premenstrual symptoms. H15: Mandala activity is more effective than education provided for coping with premenstrual syndrome in reducing premenstrual symptoms among students with PMS. Research Groups: Mandala Group, Coping with Premenstrual Symptoms Education Group, and Control Group.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 25
Healthy Volunteers: t
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• Age between 18-25 years

• Female students enrolled in the 1st and 2nd years of the Faculty of Health Sciences PMSÖ score of 110 and above

• Regular menstruation in the last six months (between 21-35 days)

• Not using any medication or non-medication methods to cope with PMS symptoms

• Not using contraceptive pills

• Absence of any gynecological diseases (abnormal uterine bleeding, fibroids, ovarian cysts, etc.)

• No diagnosis of psychiatric illness

• Not using any psychiatric medication such as antidepressants

• Absence of any condition that may hinder Mandala drawing

• No previous experience with Mandala education

• Willingness to participate in the study

• Proficiency in speaking and understanding Turkish

Locations
Other Locations
Turkey
Bilecik Şeyh Edebali University
RECRUITING
Bilecik
Contact Information
Primary
Merve SEZER YILDIZ, Ph.D. Std.
merveyildiz@bilecik.edu.tr
05301789126
Time Frame
Start Date: 2023-10-25
Estimated Completion Date: 2024-01-31
Participants
Target number of participants: 90
Treatments
Experimental: mandala
Experimental: Coping with Premenstrual Symptoms Education Group
Experimental: Control Group
Related Therapeutic Areas
Sponsors
Leads: Eskisehir Osmangazi University

This content was sourced from clinicaltrials.gov