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CompletedNCT07916454Updated Nov 6, 2026

The Effect of Music on Pain During Drain Removal

An interventional study of Music intervention in Music Intervention, sponsored by Ankara Yildirim Beyazıt University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-11-06.

Sponsored by Ankara Yildirim Beyazıt University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 2 years 7 months after the study started (first participant enrolled Mar 2024, registered Oct 2026).
Updated Nov 4, 2026Newly registeredGo to Updates ↓
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This research was conducted as a randomized controlled experimental study to examine the effect of music listening during drain removal on pain in patients undergoing total knee arthroplasty. The study was carried out between March 19, 2024, and October 15, 2025, in the orthopedics and traumatology clinic of a state hospital in Türkiye. The sample consisted of 60 adult patients. Patients were randomly divided into intervention and control groups. Patients in the intervention group were played the Acemaşiran Maqam of Turkish Classical MP3 music, prepared by the group of Turkish Music Research and Promotion (TÜMATA) in Türkiye, via headphones for a total of 30 minutes, starting 15 minutes before and continuing for 15 minutes after drain removal. Patients in the control group received no intervention. Before the drain removal procedure, the "Patient Demographic Characteristic Form" including the sociodemographic characteristics of the patients and the VAS pain scale were completed by the researcher through face-to-face interviews. Pain levels of patients were re-evaluated using the Visual Analog Scale (VAS) pain scale immediately after, and 15 minutes after drain removal. The study expected that patients in the intervention group will have more favorable pain scores compared to the control group. It is believed that the results of this research will contribute to the literature.

Read the detailed description

This research was conducted as a randomized controlled experimental study to examine the effect of music listening during drain removal on pain in patients undergoing total knee arthroplasty. The study was carried out between March 19, 2024, and October 15, 2025, in the orthopedics and traumatology clinic of a state hospital in Türkiye. Written permission was obtained from the Clinical Research Ethics Committee of a state university in Türkiye to conduct the research (Decision No: 2023-KAEK-30). The sample size was calculated using the group*time interaction (mixed ANOVA) module in repeated measures in the G-Power Version 3.1.9.6 program (Franz Faul, Germany). It was determined that a minimum of 44 patients (22 in each group) were required to determine the change before, after, and at 15 minutes in the intervention and control groups with 95% power, 0.05 type I error, and at least f=0.25 (moderate) effect size. To increase the power of the study, a total of 60 patients were included, with 30 in the intervention group and 30 in the control group. The study sample consisted of patients who volunteered and provided written consent. Patients who met the inclusion criteria and agreed to participate in the study were randomly assigned to the intervention and control groups. In the randomization process, participants were given sealed envelopes containing the names of the intervention and control groups, and the patient was asked to choose between the two envelopes. The patients were assigned to either the intervention or control group according to their choice. First, the researcher had the patients complete a "Patient Demographic Characteristic Form" containing sociodemographic characteristics (age, gender, marital status, education level, etc.) and the VAS pain scale through face-to-face interviews. The patients' drains were removed by their physician on the second postoperative day according to the procedure. Patients undergoing total knee arthroplasty received routine pain relief treatment with paracetamol vial 2*1 (intravenous) (08:00-20:00) and dexketoprofen ampoule 2*1 (intravenous) (12:00-24:00). Drain removal was performed after the patients received their paracetamol vial (intravenous) treatment in the morning. Fifteen minutes before drain removal in the intervention group, the researcher played the Acemaşiran maqam of Turkish Classical Music, MP3 through headphones, prepared by the group of Turkish Music Research and Promotion (TÜMATA), which is known in the literature (Özdemir et al., 2019; Çelebi et al., 2020) to have positive effects on pain and physiological parameters and provides relaxation. The ear headphones were disinfected with a 70% alcohol solution before being used between patients. Music was listened for a total of 30 minutes, continuing before 15 minutes and after 15 minutes of drain removal (Yarahmadi et al., 2018). Pain levels were assessed again using the VAS pain scale immediately after, and 15 minutes after drain removal. Patients in the control group received no intervention. Pain levels in the control group were also assessed using the VAS pain scale 15 minutes before, immediately after, and 15 minutes after drain removal. Pain assessment of all patients was performed by another nurse independent of the study to avoid bias.

02

Conditions studied

  • Music Intervention

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Keywords

  • Nursing
  • Pain
  • Music
  • Total knee arthroplasty
03

In context

Pain

10,054 studies on the registry are indexed under Pain; 1,649 are open to participants now.

This study's enrollment of 60 is close to the median of 66 across 8,493 interventional studies indexed under Pain.

Browse Pain studies →

Lead sponsor

Ankara Yildirim Beyazıt University is the lead sponsor of 241 studies on the registry; 54 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients aged 18 and over,
  • Who do not have any psychiatric disorders,
  • Who can speak and read Turkish,
  • Who do not have visual or hearing impairments and
  • Who volunteered to participate in the study were included.

Exclusion criteria

Exclusion Criteria:

  • The patient's voluntary withdrawal from the study,
  • Removing the ear headphones during the procedure,
  • The patient's early discharge during the implementation phase of the research,
  • The patient's inability to participate in the procedures due to changes in health status,
  • Administration of a painkiller to the patient other than paracetamol 2*1 (intravenous) and dexketoprofen ampoules 2*1 (intravenous),
  • The patient's transfer to another clinic.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    Music Intervention

    Patients in this group were given 30 minutes of music via MP3 headphones, starting 15 minutes before drain removal and continuing for 15 minutes after. Pain levels in the intervention group were assessed using the VAS pain scale 15 minutes before, immediately after, and 15 minutes after drain removal.

    Other: Music intervention

  • No intervention
    Control

    Patients in the control group received no intervention. Pain levels in the control group were also assessed using the VAS pain scale 15 minutes before, immediately after, and 15 minutes after drain removal.

Interventions

  • OtherMusic intervention

    Fifteen minutes before drain removal in the intervention group, the researcher played the music MP3 through headphones. The ear headphones were disinfected with a 70% alcohol solution before being used between patients. Music was played for a total of 30 minutes, continuing before 15 minutes and after 15 minutes of drain removal.

    Also known as: Music

06

What researchers measure

Primary outcomes

  1. Pain during drain removal in patients undergoing Total Knee Arthroplasty

    In this study, a Visual Analog Scale (VAS) was used to assess patients' pain. This scale includes a 10 cm ruler. Patients were asked to rate the pain they felt during the procedure on a scale of 1 to 10. Patients gave a score of "0" if they felt no pain and "10" if they felt unbearable pain. Patients were asked to rate the pain they felt on the VAS scale 15 minutes before, immediately after, and 15 minutes after the drain removal. At the end of the study, the scale results will be compared and evaluated for both groups.

    Time frame: 7 month

07

Study locations

1 site
  • Ankara Yildirim Beyazit University, Faculty of Health Sciences, Department of Nursing
    Ankara, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

2 registry updates since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Mar 2024 to primary completion in Apr 2024, 1 month.

Of 3,731 non-industry interventional studies with no phase under Pain, half reached primary completion within 10 months of starting (the median), counting those still running; a quarter within 4 and three quarters within 23. This study's 1 month is below that.

Counting every sponsor, half of 3,830 studies reached it within 10 months; a quarter within 4 and three quarters within 23.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 30, 2026
First posted
Nov 4, 2026
StartActual
Mar 19, 2024
Primary completionActual
Apr 19, 2024
CompletionActual
Oct 15, 2025
Last update
Nov 6, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Nov 4, 2026
Show all 2 updates
  1. Nov 6, 2026
    Minor edits only
    + 1 other change: conditions
  2. Nov 4, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

10

Registry details

Key details

Study ID
NCT07916454
Responsible party
Sponsor
First posted
Nov 4, 2026
Start date
Mar 19, 2024
Primary completion
Apr 19, 2024
Completion
Oct 15, 2025
Last update
Nov 6, 2026

Study contacts

Ebru Erek Kazan
study director · Ankara Yildirim Beyazit University, Faculty of Health Sciences, Department of Nursing, Esenboga Campus, Cubuk/Ankara

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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