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

NCT06193967 · ClinicalTrials.gov registry record · NA

Enhancing Child Dietary Self-monitoring

A NA study, sponsored by The University of Tennessee, Knoxville.

Completed
Registry status
NA
Development phase
19
Enrollment target

NCT06193967: Completed NA study, sponsored by The University of Tennessee, Knoxville.

NCT06193967 is a NA study that has completed, run by The University of Tennessee, Knoxville. The registered enrollment target is 19 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT06193967, a NA study, has completed, sponsored by The University of Tennessee, Knoxville.

COMPLETED
Registry status
NA
Development phase
19 participants
Enrollment target

Study Summary

The goal of this clinical trial was to test the preliminary efficacy of a digital dietary self-monitoring (dDSM) log that uses positive reinforcement strategies (caregiver praise and gamification) to improve child engagement in DSM. The main aims were to: * Conduct a proof-of-concept trial that examines the effects of positive reinforcement on child DSM behaviors. * Explore differences in children's intrinsic motivation. Participating children will be instructed to self-monitor their daily intake of targeted food groups (fruits, vegetables, sweet and salty snack foods, and sugar-sweetened beverages) for 4 weeks using a personal web-based DSM log. Each child-caregiver dyad will be randomly assigned to 1 of 4 conditions: BASIC, PRAISE, GAME, or PRAISE+GAME. For PRAISE and PRAISE+GAME conditions, caregivers will be instructed to provide daily process praise to their child related to DSM behaviors. For GAME and PRAISE+GAME conditions, logs will integrate three game mechanics: points, levels, and a virtual pet. Points will be accumulated for engaging in DSM behaviors, and accrual of points will evolve a virtual pet over time.

Primary Outcome

I.e., number of days with any logging. DSM frequency has been shown to predict success in family-based based childhood overweight and obesity programs. A day will be counted as "tracked" if any food or beverage is logged on that day or, if no food or beverage is logged, the "Logging Complete" button is clicked.

Interventions

  • BEHAVIORAL Gamification
  • BEHAVIORAL Caregiver Praise

Trial Details

FieldValue
Enrollment Target 19 participants
Start Date 2024-04-04
Est. Completion 2024-12-04
Phase NA

What the finished NCT06193967 record still lists

NCT06193967 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 19 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

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

NCT06193967 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06193967 about?

NCT06193967 is a clinical study titled "Enhancing Child Dietary Self-monitoring". The goal of this clinical trial was to test the preliminary efficacy of a digital dietary self-monitoring (dDSM) log that uses positive reinforcement strategies (caregiver praise and gamification) to improve child engagement in DSM. The main aims were to: * Conduct a proof-of-concept trial that exa...

What is the current status of trial NCT06193967?

This trial is currently completed. It is a NA study. The enrollment target is 19 participants. The study started on 2024-04-04. Estimated completion is 2024-12-04.

What interventions are being tested in trial NCT06193967?

The interventions under investigation include: Gamification (BEHAVIORAL), Caregiver Praise (BEHAVIORAL).

Who is sponsoring clinical trial NCT06193967?

This trial is sponsored by The University of Tennessee, Knoxville, which has 81 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06193967's enrollment target sits among peer trials

19 1861st of 2000 higher than 138 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

  • NCT03207464 · 19 participants · Phase 1

    Molecular Imaging of NET Using [C-11]MRB-PET in MS

  • NCT04318717 · 19 participants · Phase 2

    Pembrolizumab and Hypofractionated Radiation Therapy for the Treatment of Mucosal Melanoma

  • NCT05103904 · 19 participants · Phase 2

    Lenvatinib for the Treatment of Recurrent Hepatocellular Carcinoma After Liver Transplant

  • NCT05607407 · 19 participants · Phase 2

    Methimazole in Patients With Progressive Glioblastoma

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 NCT06193967, the US trial registry maintained by the National Library of Medicine. NCT06193967 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.