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

NCT03245775 · ClinicalTrials.gov registry record · NA

A Trial of Two Family-based Childhood Obesity Treatment Programs

A NA study, sponsored by University of Virginia.

Completed
Registry status
NA
Development phase
267
Enrollment target

NCT03245775: Completed NA study, sponsored by University of Virginia.

NCT03245775 is a NA study that has completed, run by University of Virginia. The registered enrollment target is 267 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03245775, a NA study, has completed, sponsored by University of Virginia.

COMPLETED
Registry status
NA
Development phase
267 participants
Enrollment target

Study Summary

The primary aim is to determine the relative effectiveness in child BMI z-scores at 3, 6, and 12-months post baseline of iChoose+ versus Family Connections. Secondary aims are to determine (1) ongoing reach, fidelity, and implementation costs, (2) community capacity for implementation and sustainability, (3) relative impact on family eating/physical activity and parental weight, and (4) relative adherence and potential dose response relationships.

Primary Outcome

child BMI is converted to a BMI Z score which uses a standardized distribution. A BMI z score of 0 indicates an average BMI for the childs height, weight, age, and gender. Positive z-scores indicate the number of standard deviations above the norm, while negative numbers indicate the number of standard deviations below the norm. Higher z scores indicate a greater BMI status for the child. The primary outcome is a change score, or the difference between the 6 month BMI z-score and the Baseline BM

Interventions

  • BEHAVIORAL iChoose
  • BEHAVIORAL Family Connections

Trial Details

FieldValue
Enrollment Target 267 participants
Start Date 2017-06-01
Est. Completion 2020-06-30
Phase NA
University of Virginia

449 total trials

What the finished NCT03245775 record still lists

NCT03245775 is an interventional study that assigns participants to a tested intervention. The registered 267 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 (81% lower).

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

NCT03245775 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03245775 about?

NCT03245775 is a clinical study titled "A Trial of Two Family-based Childhood Obesity Treatment Programs". The primary aim is to determine the relative effectiveness in child BMI z-scores at 3, 6, and 12-months post baseline of iChoose+ versus Family Connections. Secondary aims are to determine (1) ongoing reach, fidelity, and implementation costs, (2) community capacity for implementation and sustainabi...

What is the current status of trial NCT03245775?

This trial is currently completed. It is a NA study. The enrollment target is 267 participants. The study started on 2017-06-01. Estimated completion is 2020-06-30.

What interventions are being tested in trial NCT03245775?

The interventions under investigation include: iChoose (BEHAVIORAL), Family Connections (BEHAVIORAL).

Who is sponsoring clinical trial NCT03245775?

This trial is sponsored by University of Virginia, which has 449 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03245775's enrollment target sits among peer trials

267 395th of 2000 higher than 1,606 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

  • NCT04997109 · 267 participants · NA

    Telemedicine in Early Childhood Constraint Therapy in Cerebral Palsy

  • NCT05355701 · 267 participants · Phase 1

    A Study to Learn About the Study Medicine Called PF-07799933 in People With Advanced Solid Tumors With BRAF Alterations.

  • NCT06203509 · 267 participants · NA

    Improving Care Transitions for Medicaid Insured Individuals With Co-occurring Serious Mental Illness

  • NCT05000632 · 268 participants · NA

    Smoke Free SafeCare: Establishing a Smoke Free Home in CPS-involved Families

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 NCT03245775, the US trial registry maintained by the National Library of Medicine. NCT03245775 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.