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Completed

NCT Number: NCT04372511

Use of Binaural Beats for Colonoscopy

Investigators verify the effectiveness of "binaural beats" to reduce pain during colonoscopy .

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Santa Maria Maddalena Hospital

Volterra, Pisa, 56048, Italy

About this study

Colonoscopy is a disturbing and painful procedure, so whenever possible it is performed in sedation. Although the use of sedative drugs is effective in relieving anxiety and pain such drugs can cause significant side-effects.

This study examines the effect of Binaural Beats stimulation on pain perception during colonscopy.

Binaural Beats is a simple technique, described for the first time since by Gerald Oster , that include the presentation of two acoustic stimuli with similar frequencies through the two channels of stereo headphones. The interference of their waves which occurs at the level of the central nervous system, produces a composite signal with a frequency resulting from the difference of the two original frequencies. For example if you give an acoustic stimulus of 100 Hz to an ear and simultaneously administering another acoustic stimulation of 104 Hz to the opposite ,ear the person who listens to these stimuli will perceive a "Binaural Beat" of 4 Hz caused by the difference between the two frequencies.

These Binaural Beats are of interest because they have been thought to cause hemispheric synchronization and influence the EEG frequency like light stimulation .

Binaural Beats have already been used in humans undergoing outpatient surgery in urogynecological and have been shown to help increase patient comfort by reducing the state of anxiety and pain without interfering negatively with postoperative functional recovery . In this study the investigators evaluate the use of Binaural Beat in outpatients to undergo colonoscopy to reduce pain .

A total of 100 patients divided into two groups, 50 treatment and 50 control will be considered.

Both patient groups will be invited to wear headphones regardless of whether they have been randomized to Binaural Beats with white noise or white noise only to ensure blindness of participation The headphones will be worn ten minutes before and throughout the procedure. Pain will be measured by VAS scale and satisfaction by Likert scale after the procedure in both groups. Blood pressure and heart rate will be monitored before, during, and after the procedure.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients scheduled for outpatient colonoscopy
  • Valid consent expression to the study participation
  • Good collaboration in activities provided by the study

Exclusion criteria

  • Insufficient degree of collaboration
  • Abnormal hearing
  • Denial of informed consent to participate in the study
  • Previous colon resection surgery

Treatment and study plan

Binaural Beats

Device

Device: Sound with Binaural Beats at acoustic frequencies of 256 Hz in one ear and 260 Hz in the opposite ear producing a binaural beat of 4 Hz with a white background noise

Primary outcomes

  1. Pain perception evaluated with VAS

    Time frame: 5 minutes after completing the procedure (complete withdrawal of the colonoscope)

    Comparison between the two groups of pain perceived during the procedure by VAS scale. The Visual Analogue Scale (VAS) is a validated scale for measuring pain on 11 points, from 0 to 10, in which the patient indicates the maximum perceived pain.

Secondary outcomes

  1. Comparison between the two groups of the level of satisfaction: Likert scale

    Time frame: 5 minutes after completing the procedure (complete withdrawal of the colonoscope)

    Comparison between the two groups of the level of satisfaction of the entire procedure measured with a Likert scale . Likert scale is a scale which is used to allow the individual to express how much they agree or disagree with a particular statement patient satisfaction rated as: not at all, very low, moderate satisfaction, complete satisfaction; (b) willingness to repeat the procedure in the future:

    not at all, very low, barely yes, yes;

  2. Blood pressure assessment

    Time frame: 3 minutes before inserting the colonoscope (this was baseline), 5 minutes after colonoscope insertion and 3 minutes after completing the procedure (complete withdrawal of the colonoscope);

    Systolic and diastolic blood pressure evaluation measured in millimeters of Hg

  3. Heart rate assessment

    Time frame: 3 minutes before inserting the colonoscope (this was baseline), 5 minutes after colonoscope insertion and 3 minutes after completing the procedure (complete withdrawal of the colonoscope);

    Heart rate evaluation measured in beats/min.

  4. comparison on the number of subjects who could not complete the exam

    Time frame: at the end of the planned study in a year

    comparison on the number of subjects between the two groups who could not complete the exam due to intolerance

  5. comparison on the use of drugs during the procedure

    Time frame: at the end of the planned study in a year

    comparison between the two groups on the use of atropine during the procedure to reduce vagal effects

Sponsors and collaborators

Lead sponsor

Azienda USL Toscana Nord Ovest

Other

Registry information

Official study title

Evaluation of Pain and Patient Satisfaction Using Binaural Beats in Patients Submitted to Colonoscopy

Important dates

Study start
2020
Primary completion
2021
Study completion
2021
First posted
May 4, 2020
Registry last updated
Aug 19, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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