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The Effects Of Music In Retrograde Intrarenal Surgery

A

Afyonkarahisar Health Sciences University

Status

Completed

Conditions

Retrograde Intrarenal Surgery

Treatments

Other: Music Listening

Study type

Interventional

Funder types

Other

Identifiers

NCT04500054
(2019/165

Details and patient eligibility

About

This study aimed to investigate the effect of music listening during the preoperative and postoperative stages in patients undergoing retrograde intrarenal surgery(RIRS) on basic life findings, anxiety, pain, and the amount of analgesic used. This is a randomized controlled experimental study.

The study was conducted with two groups: the intervention group (n=30) and control group (n=30). The control group received standard care. In contrast, the intervention group, in addition to standard care, was listened to the music by the researchers for 15 minutes one hour before their surgery.

Enrollment

60 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 18 years of age or above,
  • had elective RIRS,
  • without hearing/speech impairment,
  • without mental problems,
  • without a diagnosis of psychiatric disorders,
  • without a diagnosis of depression,
  • had the surgery under general anesthesia,
  • and volunteered to participate.

Exclusion criteria

  • Patients under 18 years of age,
  • with hearing/speech impairment,
  • with mental problems,
  • with a diagnosis of psychiatric disorders,
  • with a diagnosis of depression,
  • undergoing the surgery through spinal anesthesia,
  • not willing to participate in the study

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

60 participants in 2 patient groups

Music Intervention Group
Experimental group
Description:
The music intervention group listened to the music by the researchers for the duration of 15 minutes one hour before the surgery as well as the standard care.
Treatment:
Other: Music Listening
No Intervention Group
No Intervention group
Description:
The control group patients received standard care only.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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