Ignite Creation Date:
2024-06-16 @ 11:49 AM
Last Modification Date:
2024-10-26 @ 3:31 PM
Study NCT ID:
NCT06436872
Status:
COMPLETED
Last Update Posted:
2024-05-31
First Post:
2024-03-19
Brief Title:
The Effect of Informing the Relatives of Patients Undergoing Open Heart Surgery
Sponsor:
Trakya University
Organization:
Trakya University
Study Overview
Official Title:
The Effect of Informatıon Provıded to the Relatıves of Patıents Undergoıng Open Heart Surgery on the Qualıty of Lıfe and Caregıver Burden
Status:
COMPLETED
Status Verified Date:
2024-05
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 goal of this type of study clinical trial is to determine the effect of informing the relatives of patients undergoing open heart surgery on the patients quality of life and caregiver burdenThe main question it aims to answer are
H1 Informing caregivers of patients undergoing open heart surgery improves the quality of life of patients
H2 Informing caregivers of patients undergoing open heart surgery reduces caregiver burdenRelatives of patients who have undergone open heart surgery will be informed about home care before discharge The researcher will compare the study group with the control group to see if the information given to the caregiver makes a difference on the patient39s quality of life
H1 Informing caregivers of patients undergoing open heart surgery improves the quality of life of patients
H2 Informing caregivers of patients undergoing open heart surgery reduces caregiver burdenRelatives of patients who have undergone open heart surgery will be informed about home care before discharge The researcher will compare the study group with the control group to see if the information given to the caregiver makes a difference on the patient39s quality of life
Detailed Description:
In the study patients were assigned to the study and control groups via the randomizerorg website
The Caregiver Information Form was administered by the nurse researcher in a face-to-face meeting with the caregiver The Patient Introduction Form was filled out by the researcher from the patients files The Multidimensional Quality of Life Scale was administered by the researcher through a face-to-face interview with the patient The Caregiving Burden Scale was introduced to the caregiver by the researcher and filled in by the caregiver himself The Caregiver Tracking Form prepared to track the patient and the caregiver was applied to the caregiver by the researcher in order to determine the caregivers zero point The first data collection was carried out 48 hours after the patient was admitted to the service and before information was given Caregivers in the study group were given 45 minutes of training and a booklet in line with the training booklet prepared according to daily life activities aimed at improving the patients quality of life and reducing the caregivers care burden The caregivers in the study group were given the researchers contact number and were able to reach the researcher whenever they needed
Patients in the control group underwent standard procedure No information training booklet or contact number was provided The Caregiver Information Form was administered by the researcher in a face-to-face meeting with the caregiver The Patient Introduction Form was filled out by the researcher from the patients files Multidimensional Quality of Life Scale was administered by the researcher The Caregiving Burden Scale was introduced to the caregiver by the researcher and filled in by the caregiver himself The Caregiver Tracking Form prepared to track the patient and the caregiver was applied to the caregiver by the researcher in order to determine the caregivers zero point Initial data were collected between 48 hours after the patient was admitted to the ward and before discharge
Caregiving burden scale and multidimensional quality of life form were applied to both groups at the 4th week 8th week and 12th week Patients in the intervention group were informed again according to their needs
The Caregiver Information Form was administered by the nurse researcher in a face-to-face meeting with the caregiver The Patient Introduction Form was filled out by the researcher from the patients files The Multidimensional Quality of Life Scale was administered by the researcher through a face-to-face interview with the patient The Caregiving Burden Scale was introduced to the caregiver by the researcher and filled in by the caregiver himself The Caregiver Tracking Form prepared to track the patient and the caregiver was applied to the caregiver by the researcher in order to determine the caregivers zero point The first data collection was carried out 48 hours after the patient was admitted to the service and before information was given Caregivers in the study group were given 45 minutes of training and a booklet in line with the training booklet prepared according to daily life activities aimed at improving the patients quality of life and reducing the caregivers care burden The caregivers in the study group were given the researchers contact number and were able to reach the researcher whenever they needed
Patients in the control group underwent standard procedure No information training booklet or contact number was provided The Caregiver Information Form was administered by the researcher in a face-to-face meeting with the caregiver The Patient Introduction Form was filled out by the researcher from the patients files Multidimensional Quality of Life Scale was administered by the researcher The Caregiving Burden Scale was introduced to the caregiver by the researcher and filled in by the caregiver himself The Caregiver Tracking Form prepared to track the patient and the caregiver was applied to the caregiver by the researcher in order to determine the caregivers zero point Initial data were collected between 48 hours after the patient was admitted to the ward and before discharge
Caregiving burden scale and multidimensional quality of life form were applied to both groups at the 4th week 8th week and 12th week Patients in the intervention group were informed again according to their needs
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