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
2 other identifiers
observational
101
1 country
1
Brief Summary
This study investigates the impact of lucid dreaming on individuals and explores methods to increase the likelihood of inducing lucid dreams intentionally. This study explores the impact of lucid dreaming on individuals, examining how this unique state of consciousness affects mental and emotional well-being. It further explores various methods aimed at increasing the likelihood of intentionally inducing lucid dreams. By analyzing scientific literature and experimental findings, the research highlights the potential therapeutic and creative benefits of lucid dreaming. Additionally, the study offers practical techniques designed to enhance the frequency of lucid dreams, such as maintaining a dream journal, eye movement before sleep, and recall of memories. These approaches provide individuals with tools to harness the power of lucid dreaming for personal growth and self-discovery.This study highlights the potential benefits of lucid dreaming and provides practical techniques for enhancing its frequency.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jan 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
January 9, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 26, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
May 2, 2024
CompletedFirst Submitted
Initial submission to the registry
May 21, 2024
CompletedFirst Posted
Study publicly available on registry
June 3, 2024
CompletedJune 3, 2024
May 1, 2024
4 months
May 21, 2024
May 28, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Testing the likelihood of Lucid Dreaming in Participants
Measuring the likelihood of lucid dreaming with the implementation of the methods mentioned in the behavioural section of this study.
4 months
Study Arms (3)
Placebo Group
Detailed in study, no dosages, no drugs used.
Actual Group
Detailed in study, no dosages, no drugs used.
Standard Assessment Group
Detailed in study, no dosages, no drugs used.
Interventions
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.
Eligibility Criteria
Young, healthy, individuals with no previous record of medical sleep conditions.
You may qualify if:
- Normal blood pressure, Healthy weight, no record of sleep apnea, no difficulty sleeping, ages between 18-30 only.
You may not qualify if:
- Overweight(muscle being taken into consideration, not using BMI), high or low blood pressure,
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Reserology Research
London, DN3 6GB, United Kingdom
Related Publications (1)
Greenwald B, Lombard LA, Watanabe TK. Managing sleepiness after traumatic brain injury. PM R. 2011 May;3(5):480-5. doi: 10.1016/j.pmrj.2011.04.010. No abstract available.
PMID: 21570037RESULT
Biospecimen
All records of participants and randomly selected individuals are kept.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Abdelraheem Mohamed
Reserology Research Foundation
Study Design
- Study Type
- observational
- Observational Model
- OTHER
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Research Director
Study Record Dates
First Submitted
May 21, 2024
First Posted
June 3, 2024
Study Start
January 9, 2024
Primary Completion
April 26, 2024
Study Completion
May 2, 2024
Last Updated
June 3, 2024
Record last verified: 2024-05
Data Sharing
- IPD Sharing
- Will not share
Privacy reasons as requested by participants when signed up contractually.