Personalized Music Impact on Dreaming During Propofol Sedation
This study aims to investigate how personalized music during propofol sedation affects your dreaming experience, focusing on whether you dream and how pleasant those dreams are.
Preferred Music
+ Matched Non-Preferred Music
+ Silence (Headphones Only)
Supportive Care Study
Summary
Study start date: December 19, 2025
Actual date on which the first participant was enrolled.This study is about understanding how personalized music and auditory stimulation can impact dreaming during sedation using Propofol, a common sedative. The study focuses on adults who are undergoing elective procedures under spinal anesthesia or peripheral nerve block with propofol sedation. The goal is to see if preferred music can increase dreaming and make it more pleasant, which could potentially improve the overall experience of sedation. This research is important as it could lead to better ways of managing patient comfort during medical procedures. Participants in this study are randomly assigned to one of three groups: Preferred Music, Matched Non-preferred Music, or Silence. Those in the Preferred Music group select a personally meaningful track that is played on loop through headphones during sedation. The Matched Non-preferred Music group listens to a pleasant non-selected track that is similar to the preferred selection in terms of tempo, genre, and loudness. The Silence group wears headphones but does not hear any music. The effects of the music are then measured by assessing dream incidence and dream pleasantness. Dream incidence is determined by asking participants if they had a dream, while dream pleasantness is rated on a scale from 0 to 10. The study also looks at other factors like patient satisfaction, sedative dose, and recovery endpoints.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.300 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 19 to 70 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.3 intervention groups are designated in this study
33.333% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalGroup III
PlaceboStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
IRB of Wonkwnag University Hospital
Iksan, South KoreaOpen IRB of Wonkwnag University Hospital in Google Maps