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

NCT06503159 · ClinicalTrials.gov registry record · NA

Hippocampal Network Changes Following Mindfulness Training in Tobacco Vaping Adolescents in an Open-label, Pilot Study

A NA study, sponsored by National Institute on Drug Abuse (NIDA).

Terminated
Registry status
NA
Development phase
14
Enrollment target

NCT06503159: Clinical Trial NA study, sponsored by National Institute on Drug Abuse (NIDA).

NCT06503159 is a NA study that was terminated before completion, run by National Institute on Drug Abuse (NIDA). The registered enrollment target is 14 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

NCT06503159, a NA study, was terminated before completion, sponsored by National Institute on Drug Abuse (NIDA).

TERMINATED
Registry status
NA
Development phase
14 participants
Enrollment target

Study Summary

The purpose of this translational bench-to-bedside study is to examine the neurobiological effects of an evidence-based technology-delivered mindfulness training (MT) program on vaping-related rsFC alterations in hippocampal networks and testing whether changes in rsFC ((Delta)rsFC) in these networks predict reduction in tobacco vaping behaviors in adolescents. The study also aims to test the accessibility and feasibility of using this mindfulness-based stress reduction (MBSR) platform as an implementation for widespread MT in adolescents.

Primary Outcome

The change in brain connectivity network from baseline (pre mindfulness-based stress reduction (MBSR) training) to post MBSR functional magnetic resonance imaging (fMRI) brain scan. Analysis will be done as change in brain network connectivity based on pre and post MBSR fMRI scan. Change = post-pre values

Interventions

  • BEHAVIORAL Mindfulness-based Stress Reduction (MBSR) Program
  • OTHER functional magnetic resonance imaging (fMRI)

Trial Details

FieldValue
Enrollment Target 14 participants
Start Date 2025-05-07
Est. Completion 2025-09-11
Phase NA

Why NCT06503159 stopped before completion

NCT06503159 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 14 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 Mindfulness-based Stress Reduction (MBSR) Program is the first listed.

NCT06503159 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06503159 about?

NCT06503159 is a clinical study titled "Hippocampal Network Changes Following Mindfulness Training in Tobacco Vaping Adolescents in an Open-label, Pilot Study". The purpose of this translational bench-to-bedside study is to examine the neurobiological effects of an evidence-based technology-delivered mindfulness training (MT) program on vaping-related rsFC alterations in hippocampal networks and testing whether changes in rsFC ((Delta)rsFC) in these network...

What is the current status of trial NCT06503159?

This trial is currently terminated. It is a NA study. The enrollment target is 14 participants. The study started on 2025-05-07. Estimated completion is 2025-09-11.

What interventions are being tested in trial NCT06503159?

The interventions under investigation include: Mindfulness-based Stress Reduction (MBSR) Program (BEHAVIORAL), functional magnetic resonance imaging (fMRI) (OTHER).

Who is sponsoring clinical trial NCT06503159?

This trial is sponsored by National Institute on Drug Abuse (NIDA), which has 335 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06503159's enrollment target sits among peer trials

14 1909th of 2000 higher than 90 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

  • NCT02523092 · 14 participants · Phase 4

    Use of CXCL9 as a Biomarker of Acthar Efficacy

  • NCT04263285 · 14 participants · NA

    Treatment of Depression Post-SCI

  • NCT04743271 · 14 participants · NA

    Food and Circadian Timing

  • NCT05065671 · 14 participants · Phase 1

    Microbiome Derived Metabolism and Pharmacokinetics

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

  • NCT06358040 · started 2026-10 · NA

    Opioid Dispenser for Microdiscectomy/Laminectomy

Source: ClinicalTrials.gov NCT06503159, the US trial registry maintained by the National Library of Medicine. NCT06503159 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.