Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06293248
Other study ID # 77979112
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date July 10, 2023
Est. completion date May 31, 2024

Study information

Verified date March 2024
Source Kocaeli University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was planned to examine the effect of music application on recovery in patients undergoing coronary angiography (CAG) and to obtain the opinions of patients and nurses about music.This study was conducted to examine the effect of music application on recovery in patients undergoing CAG and to obtain the opinions of patients and nurses about music.The study was planned as a pre-test, post-test design, single-center, randomized controlled experimental study. The study is planned to be conducted in the CAG unit of a university hospital between July 2023 and December 2023, the study sample will be composed of a total of 210 individuals, 105 in each group (music applied group before and after the procedure = 105, control group = 105) To collect data in the study, the "Patient Information Form", Vital Signs Evaluation Form", "Numerical Rating Scale", State-Trait Anxiety Inventory, "Perianesthesia Comfort Scale" and "Patient Satisfaction Survey on Nursing Care Quality" were used.


Description:

In the study, before the patients in the music group (MG) who would undergo planned CAG listened to music, while the patients were in the ward before the procedure; Patient information form, vital signs registration form, numerical rating scale, state-trait anxiety scale were applied, then 15-20 minutes. Music prepared with expert suggestions (Rast, Acemasiran, and Huseyni modes) 15-20 min. was listened to. After the procedure, patients in MG are given 15-20 minutes before being discharged. music was played. Then, the vital signs registration form, Numerical Rating Scale, state-trait anxiety scale, Perianesthesia Comfort Scale, and Patient Satisfaction Survey on Nursing Care Quality were administered for the last time. The specified survey forms were applied to the patients in Control Group before and after the procedure, and they were not allowed to listen to music.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 210
Est. completion date May 31, 2024
Est. primary completion date December 31, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - being between the ages of 18-65, - being literate, - having no communication or hearing impairment or neurological-psychiatric disease, - not taking sedatives before the procedure - not having undergone PCI before - being in the waiting room at least 20 minutes before the procedure. Exclusion Criteria: - Under the age of 18 - Do not speak Turkish - Have a hearing problem - Without a place and time orientation - Have any psychiatric illness - Using sedative or analgesic drugs in the last 24 hours - To be intervened outside the femoral area - Previous angiography procedure - Non-volunteer individuals will not be included in the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
musical application
Rast, Acemasiran, and Huseyni from Classical Turkish Music modes were optionally offered to the patients in the music group, and the patient's preferred music was listened to through headphones for 15-20 minutes before the CAG procedure. Following the interviews, musical genres were arranged as instrumental, without words, at 70 decibels in terms of rhythm and duration, at approximately 60 metronomes per minute, and were played according to the person's preference. Instrumental music was loaded onto the portable MP3 player provided by the researchers.

Locations

Country Name City State
Turkey Kocaeli University Hospital Kocaeli Umuttepe Campus, Izmit

Sponsors (1)

Lead Sponsor Collaborator
Kocaeli University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Means of subjective pain scores Numerical Rating Scale was used to measure the pain intensity of the patients. This scale, which aims to determine the pain intensity of patients regarding the procedure area, aims to explain the patient's pain with numbers.It is stated that numerical scales are more widely adopted by patients because they facilitate the definition of pain intensity, facilitate scoring and recording, and are useful in floor and ceiling effect assessment. The form ranging from 0 to 10 was used in the research. In the form, 0 points are considered "no pain", 1-3 points are considered "mild pain", 4-6 points are considered "moderate pain", and 7 and above points are considered "severe pain". before and up to 30 minutes after the coronary angiography
Primary Means of body temperature (0C) It will be measured by the researcher responsible for the application using an infrared thermometer. before and up to 30 minutes after the coronary angiography
Primary Means of systolic blood pressure (mmHg) The measurement on the arm, which is not operated with a digital blood pressure meter, will be made by researcher responsible for the application. before and up to 30 minutes after the coronary angiography
Primary Means of diastolic blood pressure (mmHg) The measurement on the arm, which is not operated with a digital blood pressure meter, will be made by the researcher responsible for the application. before and up to 30 minutes after the coronary angiography
Primary Means of heart rate (/minutes) It will be measured by the researcher responsible for the application with a pulse oximeter in the unprocessed arm. before and up to 30 minutes after the coronary angiography
Primary Means of respiratory rate (/minutes) It will be counted by the researcher responsible for the application by monitoring chest movements for one minute. before and up to 30 minutes after the coronary angiography
Primary Means of oxygen saturation (%) It will be measured by the researcher responsible for the application with a pulse oximeter in the unprocessed arm. before and up to 30 minutes after the coronary angiography
Primary Means of subjective anxiety scores These scales determine state and trait anxiety levels, and include two separate sections consisting of a total of 40 items developed based on the two-factor anxiety concept. The first 20 of these measure the situation-related anxiety level, and the items from 21 to 40 measure the individual's trait anxiety level. It is stated that 20-39 points obtained from the scale are considered as "mild", 40-59 points as "moderate", 60-79 points as "severe anxiety" and 80 points as "panic". before and up to 30 minutes after the coronary angiography
Primary Means of Perianesthesia Comfort Scale Scores The Perianesthesia Comfort Scale scale which reveals the individual's thoughts, emotions, and self-understanding during the stages of the surgical process, consists of 24 items and the expressions are in Likert type ranging from 1 to 6 points. The highest total score that can be obtained from the scale is 144, and the lowest total score is 24. The average value is determined by dividing the total score obtained by the number of scale items and the result is stated in the 1-6 distribution. The highest total score that can be obtained from the scale is 144, and the lowest total score is 24. The average value is determined by dividing the total score obtained by the number of scale items and the result is stated in the 1-6 distribution. A low score indicates that comfort is bad, and a high score indicates that comfort is good. Up to 30 minutes from coronary angiography
Primary Means of Patient Satisfaction Survey on Nursing Care Quality Scores Patient Satisfaction with Nursing Care Quality Questionnaire (PSNCQQ): This scale which comprises 19 items in total, includes 4 items that evaluate the perception of general satisfaction and are not included in the calculation. A 5-point Likert-type scale is scored between "(5) excellent" and "(1) poor". The PSNCQQ, where two different methods can score, was scored by adding the scores for all items and averaging each patient. Up to 30 minutes from coronary angiography
See also
  Status Clinical Trial Phase
Recruiting NCT06052553 - A Study of TopSpin360 Training Device N/A
Completed NCT05511077 - Biomarkers of Oat Product Intake: The BiOAT Marker Study N/A
Recruiting NCT04632485 - Early Detection of Vascular Dysfunction Using Biomarkers From Lagrangian Carotid Strain Imaging
Completed NCT05931237 - Cranberry Flavan-3-ols Consumption and Gut Microbiota in Healthy Adults N/A
Completed NCT04527718 - Study of the Safety, Tolerability and Pharmacokinetics of 611 in Adult Healthy Volunteers Phase 1
Terminated NCT04556032 - Effects of Ergothioneine on Cognition, Mood, and Sleep in Healthy Adult Men and Women N/A
Completed NCT04107441 - AX-8 Drug Safety, Tolerability and Plasma Levels in Healthy Subjects Phase 1
Completed NCT04998695 - Health Effects of Consuming Olive Pomace Oil N/A
Completed NCT04065295 - A Study to Test How Well Healthy Men Tolerate Different Doses of BI 1356225 Phase 1
Completed NCT01442831 - Evaluate the Absorption, Metabolism, And Excretion Of Orally Administered [14C] TR 701 In Healthy Adult Male Subjects Phase 1
Terminated NCT05934942 - A Study in Healthy Women to Test Whether BI 1358894 Influences the Amount of a Contraceptive in the Blood Phase 1
Recruiting NCT05525845 - Studying the Hedonic and Homeostatic Regulation of Food Intake Using Functional MRI N/A
Completed NCT05515328 - A Study in Healthy Men to Test How BI 685509 is Processed in the Body Phase 1
Completed NCT05030857 - Drug-drug Interaction and Food-effect Study With GLPG4716 and Midazolam in Healthy Subjects Phase 1
Completed NCT04967157 - Cognitive Effects of Citicoline on Attention in Healthy Men and Women N/A
Recruiting NCT04714294 - Evaluate the Safety, Tolerability and Pharmacokinetics Characteristics of HPP737 in Healthy Volunteers Phase 1
Recruiting NCT04494269 - A Study to Evaluate Pharmacokinetics and Safety of Tegoprazan in Subjects With Hepatic Impairment and Healthy Controls Phase 1
Completed NCT04539756 - Writing Activities and Emotions N/A
Recruiting NCT04098510 - Concentration of MitoQ in Human Skeletal Muscle N/A
Completed NCT03308110 - Bioavailability and Food Effect Study of Two Formulations of PF-06650833 Phase 1