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RELAXaHEAD for Headache Patients (Phase III)
NCT06077838 · View on ClinicalTrials.gov ↗
Study Summary
This study is a fully powered, remote randomized control trial to evaluate RELAXaHEAD in people with migraine.
Conditions Studied
Interventions
- BEHAVIORAL RELAXaHEAD Smartphone App Version 1
- BEHAVIORAL RELAXaHEAD Smartphone App Version 2
Study Locations (1)
New York
- NYU Langone Health — New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 356 participants |
| Start Date | 2023-11-08 |
| Est. Completion | 2028-08-31 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06077838
The ClinicalTrials.gov registry entry for NCT06077838 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 356 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is NYU Langone Health, which has 1,204 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Migraine appearing as the primary indexed condition, and to 2 interventions — of which RELAXaHEAD Smartphone App Version 1 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06077838 reports 1 study location spanning 1 distinct geographic area — top geographies include New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06077838 about?
NCT06077838 is a clinical study titled "RELAXaHEAD for Headache Patients (Phase III)". This study is a fully powered, remote randomized control trial to evaluate RELAXaHEAD in people with migraine.
What is the current status of trial NCT06077838?
This trial is currently recruiting. It is a NA study. The enrollment target is 356 participants. The study started on 2023-11-08. Estimated completion is 2028-08-31.
What conditions does trial NCT06077838 study?
This clinical trial studies the following conditions: Migraine. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06077838?
The interventions under investigation include: RELAXaHEAD Smartphone App Version 1 (BEHAVIORAL), RELAXaHEAD Smartphone App Version 2 (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06077838?
This trial is sponsored by NYU Langone Health, which has 1,204 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06077838 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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