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
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.
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.
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.
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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
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.
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
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
Plan to share: No
No publications or documents are linked to this record.
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.
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 ↗
This study is completed, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.
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