Ignite Creation Date:
2024-10-26 @ 3:40 PM
Last Modification Date:
2024-10-26 @ 3:40 PM
Study NCT ID:
NCT06602128
Status:
RECRUITING
Last Update Posted:
None
First Post:
2024-09-13
Brief Title:
The Effect of Breathing Exercise on Anxiety Pain and Life Findings in Patients Undergoing Coronary Angiography
Sponsor:
None
Organization:
None
Study Overview
Official Title:
The Effect of Breathing Exercise on Anxiety Pain and Vital Signs in Patients Undergoing Coronary Angiography A Randomised Controlled Study
Status:
RECRUITING
Status Verified Date:
2024-10
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This randomised controlled trial will be conducted to evaluate the effect of breathing exercise on anxiety pain and vital signs in patients undergoing coronary angiography before angiography
Hypotheses of the study H11 The anxiety level of the patients who underwent breathing exercise is lower than the patients in the control group
H12 The pain level of the patients who underwent breathing exercise is lower than the control group H13 The vital signs of the patients who underwent breathing exercises are within normal limits compared to the control group
In the study there will be an intervention group in which breathing exercise will be applied and a control group in which no intervention will be applied
Data will be collected with the pre-test data collection form half an hour before the angiography procedure in patients in the intervention and control groups Patients in the intervention group will be given breathing exercises while patients in the control group will not be subjected to any intervention After the angioplasty procedure data will be collected from the intervention and control groups with post-test data collection forms
Hypotheses of the study H11 The anxiety level of the patients who underwent breathing exercise is lower than the patients in the control group
H12 The pain level of the patients who underwent breathing exercise is lower than the control group H13 The vital signs of the patients who underwent breathing exercises are within normal limits compared to the control group
In the study there will be an intervention group in which breathing exercise will be applied and a control group in which no intervention will be applied
Data will be collected with the pre-test data collection form half an hour before the angiography procedure in patients in the intervention and control groups Patients in the intervention group will be given breathing exercises while patients in the control group will not be subjected to any intervention After the angioplasty procedure data will be collected from the intervention and control groups with post-test data collection forms
Detailed Description:
In determining the groups simple randomisation method will be used in order to form the sample in a way to ensure equal number and random distribution of the two groups Randomisation will be done by using the website httpswwwrandomizerorg In line with the randomisation list patients who meet the inclusion criteria will be included in the intervention and control groups Inclusion in the intervention and control groups will be made by the researchers in line with the randomisation list In order for the responsible researcher to apply breathing exercises heshe has a breathing techniques coaching certificate In the research triple breathing technique full yogic breathing and square breathing technique will be used Patients will be informed about the research and their written and verbal consent will be obtained Data will be collected with the pre-test data collection form half an hour before the angiography procedure in patients in the intervention and control groups Patients in the intervention group will be given breathing exercises while patients in the control group will not be subjected to any intervention The breathing exercise will be performed as a single session and will last approximately 15-20 minutes After the angioplasty procedure data will be collected from the intervention and control groups with post-test data collection forms
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None