Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT01557621 · ClinicalTrials.gov registry record · NA

Comparative Effectiveness Trial of Two Reminder/Recall Methods to Increase Immunization Rates in Young Children

A NA study, sponsored by University of Colorado, Denver.

Completed
Registry status
NA
Development phase
68,000
Enrollment target

NCT01557621: Completed NA study, sponsored by University of Colorado, Denver.

NCT01557621 is a NA study that has completed, run by University of Colorado, Denver. The registered enrollment target is 68,000 participants, above the 1,402-participant average among 58,714 other NA trials with a reported enrollment target (4750% higher). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01557621, a NA study, has completed, sponsored by University of Colorado, Denver.

COMPLETED
Registry status
NA
Development phase
68,000 participants
Enrollment target

Study Summary

The purpose of this study is to determine if a collaborative centralized population-based reminder/recall intervention is more effective than a traditional practice-based reminder/recall intervention at increasing immunizations among young children.

Primary Outcome

The definition of up-to-date is based on the national Advisory Committee on Immunization Practices(ACIP)recommended series of antigens (4:3:1:3:3:1:3) to be received by the age of 19-20 months. Three different cohorts of children aged 19-35 months will be assessed across the 3 year study period. Outcomes from each cohort will be assessed 6 months post-intervention.

Interventions

  • BEHAVIORAL Collaborative Pop-Based R/R: Phone/Mail Group
  • BEHAVIORAL Collaborative Pop-Based R/R: Mail-Only Group
  • BEHAVIORAL Practice-based Recall

Trial Details

FieldValue
Enrollment Target 68,000 participants
Start Date 2012-09
Est. Completion 2015-12
Phase NA
University of Colorado, Denver

1,283 total trials

What the finished NCT01557621 record still lists

NCT01557621 is an interventional study that assigns participants to a tested intervention. Its 68,000 participants enrollment target places it among the larger protocols in the corpus, above the 1,402-participant average among 58,714 other NA trials with a reported enrollment target (4750% higher).

The record links to 0 conditions, and to 3 interventions - of which Collaborative Pop-Based R/R: Phone/Mail Group is the first listed.

NCT01557621 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01557621 about?

NCT01557621 is a clinical study titled "Comparative Effectiveness Trial of Two Reminder/Recall Methods to Increase Immunization Rates in Young Children". The purpose of this study is to determine if a collaborative centralized population-based reminder/recall intervention is more effective than a traditional practice-based reminder/recall intervention at increasing immunizations among young children.

What is the current status of trial NCT01557621?

This trial is currently completed. It is a NA study. The enrollment target is 68,000 participants. The study started on 2012-09. Estimated completion is 2015-12.

What interventions are being tested in trial NCT01557621?

The interventions under investigation include: Collaborative Pop-Based R/R: Phone/Mail Group (BEHAVIORAL), Collaborative Pop-Based R/R: Mail-Only Group (BEHAVIORAL), Practice-based Recall (BEHAVIORAL).

Who is sponsoring clinical trial NCT01557621?

This trial is sponsored by University of Colorado, Denver, which has 1,283 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01557621's enrollment target sits among peer trials

68,000 4th of 2000 higher than 1,997 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00009633 · 68,000 participants

    Follow-up Visit of High Risk Infants

  • NCT06903897 · 68,000 participants · NA

    Social Needs Screening and Chronic Diseases Study (WE CARE)

  • NCT04473833 · 65,000 participants · NA

    Transvaginal Ultrasonography as a Screening Method for Ovarian Cancer

  • NCT05128006 · 63,200 participants

    Direct-to-patient Teledermatology and Computer-assisted Diagnosis

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT01557621, the US trial registry maintained by the National Library of Medicine. NCT01557621 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.