In this study, it was aimed to evaluate the effectiveness of the training structured according to the PMS symptom map. This experimental (randomised-controlled) study was conducted with women of reproductive age with PMS. Women who met the inclusion criteria and volunteered to participate in the study constituted the sample of the study. As a result of block randomisation, 55 women were assigned to the intervention group and 55 women to the control group. Pre-test data were collected from the women allocated to the intervention and control groups by means of data collection tools (VAS pain scoring, DAS depression stress anxiety assessment scale, Premenstrual syndrome assessment scale and premenstrual syndrome-specific life satisfaction scale). The intervention group received a 3-session structured training according to the PMS symptom map, while the control group did not receive any intervention. Women in the intervention group completed the post-test data on the last day of the 2nd cycle after the training, while women in the control group completed the post-test data on the last day of the 2nd cycle after the pre-test.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
101
A symptom map consisting of evidence-based practices for coping with PMS symptoms was created. An educational content based on this map was prepared and applied to women with PMS to evaluate whether it was effective compared to the control group.
Sakarya University
Sakarya, Turkey (Türkiye)
Premenstrual syndrome assessment scale
a scale used to measure the degree of premenstrual syndrome
Time frame: pre-intervention, 2 month after intervention
premenstrual syndrome specific life satisfaction scale
Premenstrual syndrome specific life satisfaction scale evaluates life satisfaction of women with PMS
Time frame: pre-intervention, 2 month after intervention
DAS depression stress anxiety assessment scale
DAS depression stress anxiety assessment scale, evaluates psychological symptoms
Time frame: pre-intervention, 2 month after intervention
VAS pain score
1.421 / 5.000 VAS pain score measures pain score
Time frame: pre-intervention, 2 month after intervention
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