Self-swabs could boost cervical cancer screening in kazakhstan
NCT ID NCT07111819
First seen Aug 31, 2026 · Last updated Sep 01, 2026 · Updated 1 time
Summary
This study tests whether women in Kazakhstan will accept self-sampling kits for HPV detection, a key step in preventing cervical cancer. Researchers will distribute three different self-sampling devices to 1,000 women and survey their willingness to use them. The goal is to see if this approach can improve screening coverage, which currently reaches only about 46% of eligible women. If accepted, self-sampling could offer a more accessible alternative to clinic-based Pap tests.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Self-sampling kits for HPV detection (Evalyn Brush, Copan Self Vaginal FLOQSwabs, BGI Sentis HPV self-sampling kit)
- What this could lead to
- If women accept these kits, self-sampling could become a routine way to screen for cervical cancer in Kazakhstan, potentially increasing coverage and catching the disease earlier.
- What could go wrong
- This is a validation study, not a test of cancer outcomes. Acceptance may not translate to real-world use, and the kits may not be as accurate as clinician-collected samples.
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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1,000 people
The number who actually took part.
- Started
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Aug 2025
- Finished
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Aug 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 70 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: Eligible participants will be recruited from different outpatient clinics in Kazakhstan located in the different regions (western, eastern, northern, southern, and central parts) of the country, and must meet the following inclusion criteria: 1. age - women 18 years and older; 2. Intact uterine cervix (no prior total hysterectomy or trachelectomy); 3. ability to understand and answer questions/surveys in Kazakh, Russian or English. Exclusion Criteria: patients who are 1. younger than 18 years old, 2. women after total hysterectomy (or other surgery, when the uterine cervix is removed), 3. pregnant women, and 4. those who are not able to answer questions in Kazakh, Russian or English will be excluded.
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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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Outpatient units
Astana, 010000, Kazakhstan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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