The Effect of Informing the Relatives of Patients Undergoing Open Heart Surgery

NCT ID: NCT06436872

Last Updated: 2024-05-31

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: NA
• Total Enrollment: 94 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-05-27
• Study Completion Date: 2023-10-30

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 burden.The 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 burden.Relatives 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 patient's quality of life.

Detailed Description

In the study, patients were assigned to the study and control groups via the randomizer.org 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 caregiver's care burden. The caregivers in the study group were given the researcher's 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 caregiver's 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.

Conditions

Open Heart Surgery; Life Quality; Caregiver Burden

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: SUPPORTIVE_CARE
• Blinding Strategy: SINGLE

Study Groups

intervention group

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 patient's quality of life and reducing the caregiver's care burden. The caregivers in the study group were given the researcher's contact number and were able to reach the researcher whenever they needed.

Group Type: EXPERIMENTAL

informing patients with using a booklet

Intervention Type: OTHER

The intervention group was informed before discharge and was given an information booklet. A phone number was given so that the researcher could contact the nurse. In the 4th week, 8th week and 12th week, information was given according to the information needs of the patient and caregiver.

Control Group

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 caregiver's zero point.

Group Type: NO_INTERVENTION

No interventions assigned to this group

Interventions

informing patients with using a booklet

The intervention group was informed before discharge and was given an information booklet. A phone number was given so that the researcher could contact the nurse. In the 4th week, 8th week and 12th week, information was given according to the information needs of the patient and caregiver.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Over 65 years of age,
• Does not have any psychological problems and can communicate in Turkish
• Literate,
• Having undergone open heart surgery for the first time
• After being taken to the Cardiovascular Surgery Service, they are stable after completing the 48-hour critical period,
• Elderly individuals who agreed to participate in the research constituted the patient sample of the study.

• The person who is primarily responsible for the patient care and will accompany the patient for 12 weeks, Caregivers,
• Between the ages of 18-65,
• Does not have any psychological problems and can communicate in Turkish,
• The caregiver sample was created by caregiver individuals who agreed to participate in the research.

Exclusion Criteria

• Those with neurological or metabolic diseases that may cause functional disability
• Previously had open heart surgery
• Patients with mental and cognitive dysfunction
• Patients who did not attend at least one of the post-surgical evaluations for any reason were excluded from the sample.

• Those with neurological or metabolic diseases that may cause functional disability
• Transferring the patient care to someone else during the 12-week working period,
• Caregivers who did not attend at least one of the post-surgical evaluations for any reason were excluded from the sample.

• Minimum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Trakya University

OTHER

Sponsor Role: lead

Responsible Party

Esra Akdeniz

BSN Nurse

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Esra Akdeniz, BSN

Role: PRINCIPAL_INVESTIGATOR

Trakya Üniversite

Locations

Trakya University

Edirne, , Turkey (Türkiye)

Countries

Turkey (Türkiye)

Other Identifiers

GOBAEK-2022/206

Identifier Type: -

Identifier Source: org_study_id