The study was conducted as a randomized controlled trial to evaluate the effects of foot bath application on symptom severity, quality of life, and pain levels in women with premenstrual syndrome. The research was carried out with 92 midwifery students. While foot bath therapy was applied to the experimental group, no intervention was performed in the control group. Data were collected through face-to-face interviews using the Personal Information Form, Premenstrual Symptom Scale, Visual Analog Scale, and SF-36 Quality of Life Scale.
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Personal Information Form
Timeframe: Pretest assessments were administered to all participants in both groups before the intervention.
Premenstrual Syndrome Scale (PMSS)
Timeframe: * "Baseline 1" * "3 months later" * "4 weeks later" * "approximately 4months"
Visual Analog Scale (VAS)
Timeframe: * "Baseline 1" * "3 months later" * "4 weeks later" * "Approximately 4months"
SF-36 Short Form
Timeframe: * "Baseline 1" * "3 months later" * "4 weeks later" * "Approximately 4months"