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Recruiting

NCT Number: NCT07597603

Unconscious Mind Training

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.

Recruiting

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Key information

Age range

10 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

N/A - Remote Study

Naples, Florida, 34119, United States

Location status: Recruiting

Location contact

Matthew Quitto II

CONTACT

[email protected]

917 342 2895

About this study

This investigation will rigorously evaluate: Does H22 demonstrably lower the number of unwanted behaviors reported by participants over the trial period, indicating a tangible and measurable impact?

Timeline for Observable Results: What is the typical duration required to observe statistically significant results and behavioral changes when utilizing the H22 methodology, providing insights into its practical application and patient expectations?

To achieve these objectives, participants will engage in a structured and consistent protocol:

Daily H22 Engagement. Each volunteer will commit to performing the H22 training exercises daily for a continuous period of two weeks. This consistent engagement is crucial for assessing the cumulative impact of the intervention on unconscious conditioning.

Mid-Trial Unconscious Mind Survey: After the first week of the trial, participants will complete a specialized survey. This survey is designed to gather qualitative and quantitative data regarding perception of changes in participants unconscious thought patterns, behavioral triggers, and overall mental state as a result of H22.

Behavioral Monitoring Diary. Participants will maintain a daily diary to meticulously record the number of instances participants successfully remembered not to engage in their specified unwanted behavior. This self-reporting mechanism will provide critical empirical data to track progress and validate the effectiveness of H22 in promoting conscious control over previously unconscious actions.

Through this comprehensive approach, this study endeavors to determine if H22 offers a viable, innovative solution for behavioral modification by targeting the unconscious mind, thereby addressing a significant unmet need in personal development and therapeutic interventions.

The design of the intervention is centered around simplicity and consistency: a once-a-day engagement. This frequency is strategically chosen to:

Minimize Barriers to Entry: A short, daily commitment is less daunting than lengthy, infrequent sessions, increasing user adherence.

Promote Habit Formation: Regular, brief interaction facilitates the establishment of a sustainable routine, crucial for long-term results.

Optimize Efficacy: Consistent, focused engagement. The interventions provided by the Investigator are primarily behavioral. Investigators recognize that sustained improvement with the unconscious mind is more than just instruction; it demands a change in daily habits and a commitment to ongoing self-care.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Intervention H22

Behavioral

Unconscious Mind Training.

Primary outcomes

  1. 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

  2. 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.

Study contacts

Contact information is provided by the study sponsor or research team.

Matthew Quitto II

CONTACT

[email protected]

9173422895

Sponsors and collaborators

Lead sponsor

Dream Video LLC

Other

Collaborators

  • Dream Holdings Research

Registry information

Official study title

H22 - Unconscious Mind Training and Memory Encoding

Important dates

Study start
2027
Primary completion
2028
Study completion
2028
First posted
May 19, 2026
Registry last updated
Jul 9, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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