Can a short lesson stop late-night health searches from fueling anxiety?
NCT ID NCT07834216
First seen Sep 22, 2026 · Last updated Sep 23, 2026 · Updated 1 time
Summary
Researchers at Istanbul University are testing whether structured lessons help women in perimenopause or postmenopause use online health information more wisely. The trial enrolls 60 women aged 40 to 65 and assigns them to video-based education, Pecha Kucha-based education, or a control group with no structured lesson. The training covers how to spot reliable sources, recognize misleading content, and search in ways that reduce worry. Researchers measure changes in cyberchondria, the cycle of repeated online health searching that can increase anxiety, and in e-health literacy before the lessons, right after, and one month later.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Structured health information-seeking education delivered by video or Pecha Kucha presentation
- What this could lead to
- If the training helps, menopause clinics could offer a short lesson that teaches women to judge online health content and search without spiraling into worry.
- What could go wrong
- The study is small, with 60 women in one country, and it measures self-reported worry and confidence rather than hard health outcomes. Any benefit may fade after the one-month check.
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
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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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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2027
An estimate. Start dates often move.
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- 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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45 to 65 years
- 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: * Aged 40 to 65 years * Being in the perimenopausal or postmenopausal period * Able to read and understand Turkish * Having experience using a smartphone, the internet, or social media * Willing to participate and able to provide informed consent Exclusion Criteria: * Having a diagnosed psychiatric disorder * Having a neurological disorder that affects cognitive functioning * Having a hearing or visual impairment that prevents effective communication or participation * Having a severe health condition that prevents regular participation in the study
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As listed by the trial registrant
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How to take part
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The official record
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