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NCT01731496 · ClinicalTrials.gov registry record · NA

The Efficacy of Reminders to Complete HPV Series

A NA study, sponsored by University of Rochester.

Completed
Registry status
NA
Development phase
749
Enrollment target

NCT01731496: Completed NA study, sponsored by University of Rochester.

NCT01731496 is a NA study that has completed, run by University of Rochester. The registered enrollment target is 749 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (47% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01731496, a NA study, has completed, sponsored by University of Rochester.

COMPLETED
Registry status
NA
Development phase
749 participants
Enrollment target

Study Summary

The human papillomavirus (HPV) vaccine is routinely recommended for both adolescent girls and boys starting at age 11, although it can be offered as young as 9 years of age. This is a 3-dose series and many adolescents do not complete it after getting the first dose. This study will study how effective it will be to send reminders to parents to schedule an appointment when their child is due for the next dose of HPV. Parents can chose whether they would like a phone call or text message reminder. This study will determine if the reminders work, and if one method is better than another (phone message vs. text message).

Primary Outcome

Post intervention HPV vaccination rates will be summarized by intervention group with frequencies and proportions, and will be compared between groups using chi square or Fisher's exact test as appropriate

Interventions

  • OTHER Telephone reminder
  • OTHER Text Message reminder

Trial Details

FieldValue
Enrollment Target 749 participants
Start Date 2012-04
Est. Completion 2014-10
Phase NA
University of Rochester

636 total trials

What the finished NCT01731496 record still lists

NCT01731496 is an interventional study that assigns participants to a tested intervention. The registered 749 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (47% lower).

The record links to 0 conditions, and to 2 interventions - of which Telephone reminder is the first listed.

NCT01731496 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01731496 about?

NCT01731496 is a clinical study titled "The Efficacy of Reminders to Complete HPV Series". The human papillomavirus (HPV) vaccine is routinely recommended for both adolescent girls and boys starting at age 11, although it can be offered as young as 9 years of age. This is a 3-dose series and many adolescents do not complete it after getting the first dose. This study will study how effect...

What is the current status of trial NCT01731496?

This trial is currently completed. It is a NA study. The enrollment target is 749 participants. The study started on 2012-04. Estimated completion is 2014-10.

What interventions are being tested in trial NCT01731496?

The interventions under investigation include: Telephone reminder (OTHER), Text Message reminder (OTHER).

Who is sponsoring clinical trial NCT01731496?

This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01731496's enrollment target sits among peer trials

749 145th of 2000 higher than 1,856 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01731496, the US trial registry maintained by the National Library of Medicine. NCT01731496 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.