Recruiting

H22

Sponsor:

Dream Video LLC

Code:

NCT07597603

Conditions

Memory Encoding

Memory

Behavior Change Interventions

Habits

Eligibility Criteria

Sex: All

Age: 10 - 70+

Healthy Volunteers: Accepted

Interventions

Intervention H22

Study Details

Brief summary:

H22 - Unconscious Mind Training and Memory Encoding

Phase I

The core problem this clinical trial, H22, seeks to address is the pervasive challenge of modifying deeply ingrained, often unconscious, unwanted behaviors within the general population. Many individuals struggle with habits or actions that negatively impact quality of life, productivity, or well-being, yet conventional methods often fall short due to the unconscious nature of these behaviors.

Specifically, the trial aims to investigate the efficacy of H22, a novel intervention designed to engage and train the unconscious mind, in mitigating these unwanted behaviors. The central hypothesis guiding this research is that H22 training will empower volunteers to significantly reduce the frequency and intensity of identified unwanted behaviors.

Conditions

Memory Encoding

Memory

Behavior Change Interventions

Habits

Study ID

NCT07597603

Start date

Jul, 2027

Status verified date

Jul, 2026

Completion date

Jan, 2028

Anticipated

Primary completion date

Jan, 2028

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 10 - 70+

Healthy Volunteers: Accepted

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

Study Design

Enrollment

100 participants

Anticipated

Intervention Model

Single group

Primary purpose

Other

Interventions and Outcome Measures

Arms

experimental: H22 #1

H22 interventions are administered once daily over a period of fourteen days.

Interventions

Intervention H22

Unconscious Mind Training.

Primary outcome measure

  • Proportion of volunteers achieving measurable improvements with unconscious training following a two-week treatment protocol. [ Time Frame: From enrollment to the end of treatment at 2 weeks ]
  • Compare the number of participants experiencing treatment-related adverse events versus those with positive treatment outcomes. [ Time Frame: From enrollment to the end of treatment at 2 weeks. ]

Central Contacts and Locations

Central contacts

Locations

N/A - Remote Study

Recruiting

Naples, Florida, United States, 34119

Contacts

More Information

Sponsor

Dream Video LLC

Last update posted

Jul 9, 2026

Last verified

Jul, 2026

Keywords

  • Behavior
  • Cognitive ability
  • Unconscious mind

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Dream Video LLC on 2026-07-09.