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Unconscious Mind Training

H22 - Unconscious Mind Training and Memory Encoding

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07597603
Enrollment
100
Registered
2026-05-19
Start date
2027-07-01
Completion date
2028-01-01
Last updated
2026-07-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Behavior Change Interventions, Habits, Memory, Memory Encoding

Keywords

Behavior, Cognitive ability, Unconscious mind

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.

Detailed description

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.

Interventions

BEHAVIORALIntervention H22

Unconscious Mind Training.

Sponsors

Dream Video LLC
Lead SponsorOTHER
Dream Holdings Research
CollaboratorUNKNOWN

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
10 Years to 75 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
Proportion of volunteers achieving measurable improvements with unconscious training following a two-week treatment protocol.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.From enrollment to the end of treatment at 2 weeks.

Countries

United States

Contacts

CONTACTMatthew Quitto II
dream@dreamholdingsllc.com9173422895
STUDY_DIRECTORMatthew Quitto II

Dream Video LLC

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 10, 2026