Text messages as medicine: digital program aims to improve life with PCOS
NCT ID NCT07684430
First seen Jul 06, 2026 · Last updated Jul 07, 2026 · Updated 1 time
Summary
This study tests whether a four-week digital health education program delivered via WhatsApp can improve quality of life in women with polycystic ovary syndrome (PCOS). Seventy women aged 18–45 with PCOS are randomly assigned to receive either the digital program—30 structured messages covering lifestyle, nutrition, stress, and fertility—or routine care. Quality of life is measured before and one month after the program using a PCOS-specific questionnaire.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Digital health education program (WhatsApp-based)
- What this could lead to
- If effective, this low-cost digital program could offer a scalable way to help women with PCOS manage symptoms and improve daily well-being.
- What could go wrong
- This is a small, single-site trial with 70 participants, so results may not apply broadly. The program is educational only and does not treat the underlying condition.
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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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70 people
The number who actually took part.
- Started
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Apr 2026
- 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 to 45 years
- Sex
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Female participants only
- Healthy volunteers
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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 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: 1. Women diagnosed with polycystic ovary syndrome 2. Women aged 18-45 years 3. Women attending the selected women's health wards and gynecology clinics during the study period 4. Willingness to participate and provide written informed consent Exclusion Criteria: 1. Withdrawal of consent at any stage of the study 2. Failure to complete either the pre-test or post-test assessments 3. Incomplete participation in the educational intervention program
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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
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Pouran Varvani Farahani
Nicosia, Haspolat, Cyprus
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