- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06440226
Testing Methods to Increase the Frequency of Lucid Dreaming (RRF)
Behaviors Of Boredom, Memory, and Wakefulness, and Their Relation to Determining the Frequency of Lucid Dreaming
Study Overview
Status
Conditions
Detailed Description
This detailed study explores the profound impact of lucid dreaming on individuals and assesses various techniques designed to intentionally induce lucid dreams. Lucid dreaming, where dreamers are aware that they are dreaming and can often control their dreams' content, has long intrigued both the scientific community and the general public due to its potential for deep psychological insight and self-improvement.
The primary objective of the research was to investigate methods that could significantly increase the likelihood of inducing lucid dreams.
In continuation, the study explores various methodologies aimed at increasing the probability of individuals intentionally inducing lucid dreams. Techniques such as targeted memory reactivation, where dreamers set intentions before sleep, are scrutinized for their effectiveness. The research examines how these methods align with neuroscientific understandings of sleep phases, particularly REM sleep when lucid dreaming most frequently occurs. The correlation between sleep quality, dream recall frequency, and the propensity to experience lucid dreams is highlighted, proposing that enhancing one's sleep hygiene could indirectly foster the conditions suitable for lucid dreaming.
Analyzing extensive scientific literature and experimental data, the study discusses the uses of lucid dreaming as a cognitive tool. It examines scenarios that promote problem-solving and creative thinking through conscious navigation and manipulation of dream content. This allows individuals to rehearse skills, resolve conflicts, and explore creative avenues that may not be accessible in waking life.
Lastly, these approaches offer individuals practical tools to harness the power of lucid dreaming for personal growth and self-discovery. The study emphasizes the importance of intentionality in entering the lucid dreaming state and maintaining a mindset conducive to this during waking hours. The capacity to engage in lucid dreaming is presented as a meaningful pursuit that can contribute to one's mental health and creative expression, fostering a deeper understanding and appreciation of this complex cognitive phenomenon.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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London, United Kingdom, DN3 6GB
- Reserology Research
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Normal blood pressure, Healthy weight, no record of sleep apnea, no difficulty sleeping, ages between 18-30 only.
Exclusion Criteria:
- Overweight(muscle being taken into consideration, not using BMI), high or low blood pressure,
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
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Placebo Group
Detailed in study, no dosages, no drugs used.
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Actual Group
Detailed in study, no dosages, no drugs used.
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Participants were instructed to move their eyes as much as possible with their eyes closed just before falling asleep.
This technique aimed to mimic the Rapid Eye Movement (REM) sleep phase, which is often associated with more vivid and memorable dreams.
Another intervention involved asking participants to recall and think about their thoughts or events from the previous night before going to sleep.
This method engaged cognitive processes related to memory and reflection, potentially setting the stage for increased awareness during sleep.
Participants were also asked to recall their lucid dreams from previous nights.
This intervention seemed to activate memory and awareness related to dreaming, which significantly increased the likelihood of experiencing lucid dreams the following night.
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Standard Assessment Group
Detailed in study, no dosages, no drugs used.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Testing the likelihood of Lucid Dreaming in Participants
Time Frame: 4 months
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Measuring the likelihood of lucid dreaming with the implementation of the methods mentioned in the behavioural section of this study.
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4 months
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: Abdelraheem Mohamed, Reserology Research Foundation
Publications and helpful links
General Publications
Helpful Links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ReserologyRF
- Grantee 000010000 (Other Identifier: Reserology Research Foundation)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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