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Feasibility Testing of the "Face-Forward-Web" Program for Chronic Orofacial Pain

StatusCompleted
PhaseNot applicable
Started
View on ClinicalTrials.gov ↗

Record History

  1. Primary endpoints: details revised at 1 of 10 entries Trial completed · Final enrollment: 20 participants (planned 30) · Primary completion date changed from estimate of Jul 1, 2026 to Sep 2, 2026 · 2 more Show 5 more changesShow less
    • Trial completed
    • Final enrollment: 20 participants (planned 30)
    • Primary completion date changed from estimate of Jul 1, 2026 to Sep 2, 2026
    • Eligibility criteria expanded, about 12 words
    • Publications: details revised at 1 of 1 entry
  2. Trial status: Recruiting to Active, Not Recruiting Site details revisedv5 Show 1 more changeShow less
    • Site details revised
  3. Trial status: Not Yet Recruiting to Recruiting Enrollment target: 20 to 30 · Start date changed from estimate of Sep 1, 2025 to Sep 15, 2025 · Site details revisedv4 Show 3 more changesShow less
    • Enrollment target: 20 to 30
    • Start date changed from estimate of Sep 1, 2025 to Sep 15, 2025
    • Site details revised
  4. Secondary endpoints shortened, about 43 words Study title shortened, about 1 wordv3 Show 1 more changeShow less
    • Study title shortened, about 1 word

    See this version in full on ClinicalTrials.gov ↗

  5. Secondary endpoints: details revised at 1 of 8 entries Study description shortened, about 2 wordsv2 Show 1 more changeShow less
    • Study description shortened, about 2 words

    See this version in full on ClinicalTrials.gov ↗

  6. 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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 conduct a feasibility open pilot study (N=Up to 20) with exit interviews to assess the feasibility, acceptability, and credibility of the study protocol and Face-Forward-Web; a web-based mind-body intervention for adult patients with COP. Deliverables: \[1\] Adapt and refine open pilot protocol, patient recruitment, and other study materials. \[2\] Assess the feasibility, acceptability, and credibility of Face-Forward-Web and optimize the intervention methodology in preparation for a future efficacy study. This research leverages mixed methods information to evaluate the feasibility, acceptability, and credibility of Face-Forward-Web and optimize the intervention and study methodology in preparation for the subsequent pilot study and again later, for a pilot feasibility randomized control trial (RCT).
Trial Details
NCT Number NCT06754917
Lead Sponsor Massachusetts General Hospital
Collaborators: National Institute of Dental and Craniofacial Research (NIDCR)
Conditions Orofacial Pain, Facial Pain
Enrollment 20 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov