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.
Age range
18 Years
Sex
FEMALE
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
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"