Unconscious Mind Training for Habit Change
Official title: H22 - Unconscious Mind Training and Memory Encoding
Run by Dream Video LLC · NCT07597603 · Data updated 2026-11-12
This study tests a new program called H22 to see if it can help people reduce unwanted habits by training the unconscious mind.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 10 Years to 75 Years |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | Dream Video LLC Academic / other |
| Locations | 1 site (Naples, Florida) |
| Status | Recruiting |
| Started | July 2027 |
| Main results expected | January 2028 |
| Study ends | January 2028 |
| Registry record updated | October 7, 2026 |
| Trial ID | NCT07597603 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults who can read and write and are willing to commit to daily two-week H22 training and reporting.
✕Probably not a fit
Individuals with medical instability or factors compromising data collection may not benefit from the intervention.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
H22 is an intervention aimed at altering deeply ingrained behaviors by engaging unconscious processing. In this Phase 2.1 study, volunteers will perform daily H22 training for two weeks and complete a mid-trial survey plus keep a behavior diary to track changes. The study uses remote participation with monitoring of behavior frequency to determine if unconscious conditioning can reduce unwanted actions. Participants will be adults capable of reading and following the protocol, with data collected remotely from Naples, Florida as the lead sponsor operates. The trial seeks to quantify reductions in reported unwanted behaviors over the intervention period.
Why it matters
Potential benefit: If successful, participants may experience a reduction in the frequency and intensity of unwanted behaviors through unconscious training.
How similar studies have gone: Previous Phase 1 results in a small sample suggested potential but the approach is still under investigation and not yet proven at scale.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Can read and write * Willing and able to follow the requirements of the protocol Exclusion Criteria: \- Medical instability, restlessness, or other factors that would compromise data acquisition
Where it's running
-
N/A - Remote Study
Naples, Florida, United States Recruiting
Study contacts
- Study coordinator: Matthew Quitto II
- Email: dream@dreamholdingsllc.com
- Phone: 9173422895
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.