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

NCT05086237 · ClinicalTrials.gov registry record · NA

Well-Child Visit Trial

A NA study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
NA
Development phase
739
Enrollment target

NCT05086237: Completed NA study, sponsored by Wake Forest University Health Sciences.

NCT05086237 is a NA study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 739 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.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT05086237, a NA study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
NA
Development phase
739 participants
Enrollment target

Study Summary

This project will use Twilio as a platform for a text messaging campaign to implement timely follow up with parents/guardians of children ages 0 to 17 years who have missed Well Child Visits (WCVs). The first phase of this project was an open trial. This second phase of the study will be a randomized controlled trial (RCT) to randomly assign parents/guardians of children who missed a WCV to an intervention condition or no intervention, and assess reasons for missed visits and experiences at last visit. Parents/guardians will receive text messages notifying them of missed visits and prompting them to reschedule, as well as inviting them to complete an online survey. Each reminder message will at minimum direct parents/guardians to reschedule by phone or by the patient portal. Outcomes of the follow-up campaign will be evaluated, including rescheduled visits within 6 weeks of missed visit and attendance at rescheduled visit. This aim will incorporate patient Electronic Health Record (EHR) data into mixed effects logistic regressions for the primary study outcomes.

Primary Outcome

If parent/guardian rescheduled well child visit

Interventions

  • OTHER Text message reminders

Trial Details

FieldValue
Enrollment Target 739 participants
Start Date 2022-05-13
Est. Completion 2022-08-09
Phase NA
Wake Forest University Health Sciences

1,140 total trials

What the finished NCT05086237 record still lists

NCT05086237 is an interventional study that assigns participants to a tested intervention. The registered 739 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 1 intervention - of which Text message reminders is the first listed.

NCT05086237 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT05086237 about?

NCT05086237 is a clinical study titled "Well-Child Visit Trial". This project will use Twilio as a platform for a text messaging campaign to implement timely follow up with parents/guardians of children ages 0 to 17 years who have missed Well Child Visits (WCVs). The first phase of this project was an open trial. This second phase of the study will be a randomize...

What is the current status of trial NCT05086237?

This trial is currently completed. It is a NA study. The enrollment target is 739 participants. The study started on 2022-05-13. Estimated completion is 2022-08-09.

What interventions are being tested in trial NCT05086237?

The interventions under investigation include: Text message reminders (OTHER).

Who is sponsoring clinical trial NCT05086237?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT05086237's enrollment target sits among peer trials

739 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

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

  • NCT03723928 · 739 participants · NA

    S1703 Serum Tumor Marker Directed Disease Monitoring in Patients With Hormone Receptor Positive Her2 Negative Metastatic Breast Cancer

  • NCT03963622 · 740 participants · NA

    Careful Ventilation in Acute Respiratory Distress Syndrome (COVID-19 and Non-COVID-19)

  • NCT04074135 · 740 participants · Phase 2

    Natural History and Management of Von Hippel-Lindau (VHL) Associated Pancreatic Neuroendocrine Tumors

  • NCT05215340 · 740 participants · Phase 3

    Study of Dato-DXd Plus Pembrolizumab vs Pembrolizumab Alone in the First-line Treatment of Subjects With Advanced or Metastatic NSCLC Without Actionable Genomic Alterations

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT05086237, the US trial registry maintained by the National Library of Medicine. NCT05086237 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.