Could a smartphone app close the gap in cervical cancer Follow-Up?
NCT ID NCT04070534
First seen Aug 03, 2026 · Last updated Aug 04, 2026 · Updated 1 time
Summary
This study tests a web-based educational platform called PALS designed to improve knowledge and follow-up among women with abnormal cervical cancer screening results. Researchers will use interviews to understand women's knowledge and perceived barriers, then create educational content to address these gaps. The goal is to see if this tool can increase attendance at follow-up visits, potentially improving early detection and prevention of cervical cancer.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Patient Activated Learning System (PALS), a web-based educational platform
- What this could lead to
- If effective, this approach could improve follow-up rates after abnormal cervical cancer screenings, potentially reducing cervical cancer cases.
- What could go wrong
- The trial is small and early, and the outcome depends on whether better knowledge actually translates into more women attending follow-up visits.
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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95 people
The number who actually took part.
- Started
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Aug 2019
- Finished
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Jan 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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21 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: * All Women 21-65 years with diagnosis of abnormal pap smear presenting to Women's Health Colposcopy Clinic at WCMC * Access to a smartphone * English or Spanish Speaking Exclusion Criteria: * Pregnant women * Non-English or Spanish speakers
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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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New York Prebyterian Hospital Weill Cornell
New York, New York, 10065, United States
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