Footbath therapy shows promise for PMS relief
NCT ID NCT07461051
First seen Jun 25, 2026 · Last updated Aug 28, 2026 · Updated 2 times
Summary
This study tested whether regular footbaths during the luteal phase (the week or two before a period) could help women with premenstrual syndrome (PMS). 92 women participated, with one group receiving footbath therapy and the other receiving no treatment. Researchers measured symptom severity, pain levels, and quality of life using standard questionnaires. The goal was to see if this simple, at-home practice could offer relief without medication.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- foot bath therapy
- What this could lead to
- If it works, this could offer a simple, drug-free way to ease PMS symptoms and improve quality of life.
- What could go wrong
- This is a small, completed trial with no blinding, so results may be influenced by placebo effects. The approach is not a cure and may not work for everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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92 people
The number who actually took part.
- Started
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Sep 2025
- Finished
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Jun 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 18 and 25 years of age * Having no chronic disease * Having a symptom severity score of 5 or higher according to the VAS, * Voluntarily agreeing to participate in the study. Exclusion Criteria: * Psychiatric disorder * Secondary dysmenorrhea.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
İnonü Universty
Ağrı, Ağrı, 04100, Turkey (Türkiye)
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Other studies related to the condition(s) this trial covers.
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