- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07597603
Unconscious Mind Training
H22 - Unconscious Mind Training and Memory Encoding
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.
연구 개요
상세 설명
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.
연구 유형
등록 (추정된)
단계
- 해당 없음
연락처 및 위치
연구 연락처
- 이름: Matthew Quitto II
- 전화번호: 9173422895
- 이메일: dream@dreamholdingsllc.com
연구 장소
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Florida
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Naples, Florida, 미국, 34119
- 모병
- N/A - Remote Study
-
연락하다:
- Matthew Quitto II
- 전화번호: 917 342 2895
- 이메일: dream@dreamholdingsllc.com
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 어린이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
설명
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
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 다른
- 할당: 해당 없음
- 중재 모델: 단일 그룹 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: H22 #1
H22 interventions are administered once daily over a period of fourteen days.
|
Unconscious Mind Training.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
기간 |
|---|---|
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Proportion of volunteers achieving measurable improvements with unconscious training following a two-week treatment protocol.
기간: From enrollment to the end of treatment at 2 weeks
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From enrollment to the end of treatment at 2 weeks
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Compare the number of participants experiencing treatment-related adverse events versus those with positive treatment outcomes.
기간: From enrollment to the end of treatment at 2 weeks.
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From enrollment to the end of treatment at 2 weeks.
|
공동 작업자 및 조사자
간행물 및 유용한 링크
일반 간행물
- Meng F, Li A, You Y, Xie C. Motor expertise modulates unconscious rather than conscious executive control. PeerJ. 2019 Feb 5;7:e6387. doi: 10.7717/peerj.6387. eCollection 2019.
- Desender K, Van Lierde E, Van den Bussche E. Comparing conscious and unconscious conflict adaptation. PLoS One. 2013;8(2):e55976. doi: 10.1371/journal.pone.0055976. Epub 2013 Feb 6.
- Gantman AP, Adriaanse MA, Gollwitzer PM, Oettingen G. Why did I do that? Explaining actions activated outside of awareness. Psychon Bull Rev. 2017 Oct;24(5):1563-1572. doi: 10.3758/s13423-017-1260-5.
- Williams LE, Bargh JA, Nocera CC, Gray JR. The unconscious regulation of emotion: nonconscious reappraisal goals modulate emotional reactivity. Emotion. 2009 Dec;9(6):847-54. doi: 10.1037/a0017745.
- Bargh JA, Gollwitzer PM, Lee-Chai A, Barndollar K, Trotschel R. The automated will: nonconscious activation and pursuit of behavioral goals. J Pers Soc Psychol. 2001 Dec;81(6):1014-27.
- Bargh JA, Morsella E. The Unconscious Mind. Perspect Psychol Sci. 2008 Jan;3(1):73-9. doi: 10.1111/j.1745-6916.2008.00064.x.
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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