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

NCT06538922 · ClinicalTrials.gov registry record · NA

Developing a Digital Intervention to Prevent Risky Health Behaviors

A NA study, sponsored by University of Vermont.

Completed
Registry status
NA
Development phase
9
Enrollment target

NCT06538922: Completed NA study, sponsored by University of Vermont.

NCT06538922 is a NA study that has completed, run by University of Vermont. The registered enrollment target is 9 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

NCT06538922, a NA study, has completed, sponsored by University of Vermont.

COMPLETED
Registry status
NA
Development phase
9 participants
Enrollment target

Study Summary

The project will launch the development of Parents and Teens Together (PATT), a dyadic digital parent-teen prevention intervention, for families of young teens experimenting or at high risk for experimenting with substance use (SU) that can provide personalized support for learning and practicing evidence-based family skills. This scalable intervention will combine a blended, virtual and health coach-led, single-session intervention (SSI) for evidence-based family skills with an mHealth app delivering a just-in-time adaptive intervention (JITAI) to support the use of family skills in daily life. As a first step in the iterative design of PATT, this project will test the acceptability, feasibility and costs of the SSI and engage in a participatory design process to finalize the plan for an initial JITAI prototype. For young teens experimenting or at risk for experimenting with SU and their parents, ready access to a scalable prevention program that closely mirrors and extends the in-time support provided in behavioral family therapy is essential for SUD prevention.

Primary Outcome

Acceptability will be assessed by examining (1) single item mean scores and overall mean scores on the Program Feedback Scale, a scale used to evaluate acceptability and perceptions of SSIs, across participants. Higher scores indicated greater acceptability, range 1-5.

Interventions

  • BEHAVIORAL Single Session Family Intervention

Trial Details

FieldValue
Enrollment Target 9 participants
Start Date 2024-07-29
Est. Completion 2024-12-05
Phase NA
University of Vermont

162 total trials

What the finished NCT06538922 record still lists

NCT06538922 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 9 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 1 intervention - of which Single Session Family Intervention is the first listed.

NCT06538922 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06538922 about?

NCT06538922 is a clinical study titled "Developing a Digital Intervention to Prevent Risky Health Behaviors". The project will launch the development of Parents and Teens Together (PATT), a dyadic digital parent-teen prevention intervention, for families of young teens experimenting or at high risk for experimenting with substance use (SU) that can provide personalized support for learning and practicing ev...

What is the current status of trial NCT06538922?

This trial is currently completed. It is a NA study. The enrollment target is 9 participants. The study started on 2024-07-29. Estimated completion is 2024-12-05.

What interventions are being tested in trial NCT06538922?

The interventions under investigation include: Single Session Family Intervention (BEHAVIORAL).

Who is sponsoring clinical trial NCT06538922?

This trial is sponsored by University of Vermont, which has 162 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06538922's enrollment target sits among peer trials

9 1975th of 2000 higher than 25 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 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 NCT06538922, the US trial registry maintained by the National Library of Medicine. NCT06538922 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.