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Eating smart to beat PMS: study tests nutrition lessons for college women

NCT ID NCT06724419

Symptom relief Sponsor: Universiti Tunku Abdul Rahman Source: ClinicalTrials.gov ↗

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
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Expanded access (paused)
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Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
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Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether teaching college women about nutrition could reduce the severity of premenstrual syndrome (PMS). 210 female students aged 18-30 with mild to severe PMS took part. Researchers measured changes in PMS symptoms, stress levels, and physical activity after the nutrition education program.

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

210 people

The number who actually took part.

Started

Feb 2025

Finished

Jul 2025

Lead sponsor

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

18 to 30 years

Sex

Female participants only

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show 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: 1. Females students aged 18 to 30 years 2. PMS scores（6-36） 3. Regular menstrual cycles (defined as a menstrual cycle of 21 to 35 days) 4. Not using hormonal compounds (such as contraceptive pills), drugs (such as fluoxetine and escitalopram), or non-drug treatments affecting premenstrual syndrome, such as special diets 5. No participation in interventional studies related to premenstrual syndrome in the past 6 months Exclusion Criteria: 1. Amenorrhea 2. Polycystic ovarian disease (PCOD) 3. Those who are unable to attend according to intervention protocol

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Conditions

The condition(s) this trial relates to.

premenstrual tension

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Premenstrual syndrome-PMS

Contacts and locations

Locations

  • Hainan Vocational University of Science and Technology

    Haikou, Hainan, 570100, China

More trials for these conditions

Other studies related to the condition(s) this trial covers.