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Can an AI coach help teens manage period pain better than a teacher?

NCT ID NCT07598929

What the study statuses mean

This study's is highlighted.

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 This study
Running, but no longer taking on new participants.
Completed
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 Results may not be published yet.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
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
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
The full record has not been published yet, so there is little to show here.
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This status has not been confirmed recently, so it may be out of date.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 tests three ways to teach teen girls about managing period pain and hygiene: an AI-powered mobile app, face-to-face classes, and a brochure. About 120 girls aged 14-17 will take part, and researchers will check their knowledge and habits after 4 and 8 weeks. The goal is to see if digital tools can be as effective as traditional teaching.

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

About 120 people

The number the study aims to enrol. It can still change while the study runs.

Started

Apr 2026

Expected to finish

Jun 2026

An estimate. End dates often move.

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

14 to 17 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

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: * Being aged 14-17 years * Having experienced menarche (having an active menstrual cycle) * Having experienced dysmenorrhea at least once within the past six months * Being a high school student and having the cognitive ability to understand the educational materials * Having access to a smartphone and the internet (mandatory for the AI group; preferred for comparability across groups) * Willingness to participate in the study voluntarily * Provision of parental/legal guardian consent due to being under 18 years of age Exclusion Criteria: * Having a diagnosed chronic gynecological condition (e.g., endometriosis) * Regular use of medications that may affect the menstrual cycle * Having previously received structured menstrual health education (to minimize confounding effects)

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Conditions

The condition(s) this trial relates to.

dysmenorrhea Health Education

As listed by the trial registrant

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

Contacts and locations

Locations

  • Hacı Mehmet Sabancı Anatolian High School

    Merkez, Sivas, 58010, Turkey (Türkiye)

More trials for these conditions

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