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Meditative Neurofeedback for Depression

Study acronym: MediNF
StatusRecruiting
PhasePhase 1
Started
View on ClinicalTrials.gov ↗
Trial flagged as At Risk
Primary completion moved at least 12 months later Nov 15, 2026 → Nov 15, 2027
Primary endpoint reworded 1 of 1 changed
See other at-risk trials from University of California, San Diego

Record History

  1. Notable Primary endpoint(s) modified Phase changed: not applicable → Phase 1 · Enrollment increased: 27 → 60 participants · Interventions modified · 4 more Show 7 more changesShow less
    • Phase changed: not applicable → Phase 1
    • Enrollment increased: 27 → 60 participants
    • Interventions modified
    • Trial arms changed: 1 → 3
    • Secondary endpoints: 3 to 6
    • Site contact updated
    • Eligibility criteria expanded, about 5 words
  2. Notable Primary completion pushed from Nov 15, 2026 to Nov 15, 2027 Completion pushed from Jun 15, 2027 to Nov 15, 2027 · Site contact updated · Study description shortened, about 2 wordsv4 Show 3 more changesShow less
    • Completion pushed from Jun 15, 2027 to Nov 15, 2027
    • Site contact updated
    • Study description shortened, about 2 words

    See this version in full on ClinicalTrials.gov ↗

  3. Notable Primary completion date: Nov 15, 2025 to Nov 15, 2026 Completion date: Jun 15, 2026 to Jun 15, 2027v3 Show 1 more changeShow less
    • Completion date: Jun 15, 2026 to Jun 15, 2027
  4. Minor Site contact updatedv2
  5. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this study is to test a meditative neurofeedback intervention for depressed mood.
Trial Details
NCT Number NCT06675240
Lead Sponsor University of California, San Diego
Conditions Depression - Major Depressive Disorder, Depression Disorders
Enrollment 60 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov