Ignite Creation Date:
2024-05-06 @ 8:08 PM
Last Modification Date:
2024-10-26 @ 3:21 PM
Study NCT ID:
NCT06260085
Status:
COMPLETED
Last Update Posted:
2024-02-15
First Post:
2024-01-25
Brief Title:
Effect of Listening to Relatives Voice Recordings on Chest Pain Anxiety and Depression in Coronary ICU Patients
Sponsor:
TC ORDU ÜNİVERSİTESİ
Organization:
TC ORDU ÜNİVERSİTESİ
Study Overview
Official Title:
The Effect of Listening to the Voice Recording of Relatives on Chest Pain Anxiety and Depression in Patients Hospitalised in Coronary Intensive Care Unit Randomised Controlled Study
Status:
COMPLETED
Status Verified Date:
2024-02
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The aim of the study was to evaluate the effect of listening to the voice recordings of relatives of patients with acute myocardial infarction AMI who were treated in the coronary intensive care unit on chest pain anxiety and depression parameters of the patients
Methods In the study which was conducted as a randomised controlled experimental study voice recordings of the family members of the patients were created and played to the patients through a music pillow The study was carried out with 60 patients 30 experimental and 30 control groups Three tests were applied to the patients 15 minutes before 15 and 30 minutes after the application The data of the study were collected using the Patient Introduction Form Hospital Anxiety Depression Scale Visual Analogue Scale and Patient Follow-up Form
Methods In the study which was conducted as a randomised controlled experimental study voice recordings of the family members of the patients were created and played to the patients through a music pillow The study was carried out with 60 patients 30 experimental and 30 control groups Three tests were applied to the patients 15 minutes before 15 and 30 minutes after the application The data of the study were collected using the Patient Introduction Form Hospital Anxiety Depression Scale Visual Analogue Scale and Patient Follow-up Form
Detailed Description:
In the study it was emphasized that the messages to be played to the patient should be 3-5 minutes and simple terms should be used in a way that can be understood by individuals with low education level Written informed consent was obtained from the patient and the patients relatives before the application In the message recorded by a patients relative decided by the patients family members the patients relative said what heshe wanted to say to the patient and recorded it using a voice recorder The researcher had a preliminary interview with the patients relative before the voice recording was taken about the use of the voice recorder and the content of the message in order to prevent the messages from negatively affecting the patient The voice recording created by the patients relative was played to the patient by the researcher using a music pillow After the patient listened to the audio recording it was erased under the witness of the patients relativeIn this randomised controlled experimental study patients were randomised into intervention and control groups according to gender and age groups In the preliminary interviews with the family members of the patients in the intervention group the message content was discussed with the relatives of the patients before the voice recording was taken and carefully prepared to prevent negative effects After the patients condition was stable the pretest was administered 15 minutes before T1 the voice recording of the patients relative was played through the music pillowAfter the application two more tests were applied at 15 T2 and 30 T3 minutes After the condition of the patients in the control group was stable the pre-test was administered then the patient was given routine information Your motherfatherdaughterson is at the door is there anything you want to tell them I can convey and give feedback After the information two more tests were administered at 15 and 30 minutes
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None