Clinical trial Recruiting at 1 site Interventional Ages 10 to 75

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 typeInterventional
Ages10 Years to 75 Years
SexAll
Enrollment100 (estimated)
SponsorDream Video LLC
Academic / other
Locations1 site (Naples, Florida)
StatusRecruiting
StartedJuly 2027
Main results expectedJanuary 2028
Study endsJanuary 2028
Registry record updatedOctober 7, 2026
Trial IDNCT07597603 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

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.