Unconscious Mind Training for Memory and Habits
This study is testing a new behavioral intervention called "Unconscious Mind Training" (H22) to help people change unwanted habits and improve memory encoding. Researchers want to see if H22 can reduce unwanted behaviors and how quickly changes can be observed. You might be able to join if you are between 10 and 75 years old, can read and write, and are willing to follow the study's instructions. The study aims to enroll 100 participants. Success in this study means participants show measurable improvements in their behaviors after two weeks of training.
- Study design
- This is an interventional study with a planned enrollment of 100 participants. It is a Phase I study, meaning it's an early-stage investigation.
- What's involved
- You would perform H22 training exercises daily for two weeks. You would also complete a specialized survey after one week and keep a daily diary to track your behaviors.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your progress will be measured from enrollment to the end of treatment at two weeks.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Unconscious Mind Training
At a glance
Conditions
NCT07597603
Where you'd take part
This study runs at 1 site. They're the same protocol — you choose where, and that choice sets who your contact draft is addressed to.
N/A - Remote Study
Naples, Floridastudy coordinator listed
Recruiting
Sites open and close at different times, so the status above is per site — it can differ from the study's overall status.
Study leadership
- Matthew Quitto II · STUDY_DIRECTOR · Dream Video LLC
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
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Inclusion
What this trial measures
- 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.