Psychosocial Nursing Interventions on Sleep, Anxiety and Delirium in Patients Undergoing Open Heart Surgery
NCT ID: NCT05864482
Last Updated: 2023-09-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
60 participants
INTERVENTIONAL
2023-05-09
2023-11-30
Brief Summary
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Are psychosocial nursing interventions applied to a patient with cardiac surgery effective in preventing delirium?
Are psychosocial nursing interventions applied to a patient with cardiac surgery effective on sleep quality?
Are psychosocial nursing interventions applied to a patient with cardiac surgery effective on the level of anxiety?
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
DOUBLE
Study Groups
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Experimental
Brief Cognitive behavioral therapy intervention will be interviewed by the researcher as part of psychosocial care, with two sessions pre-operative and two post-operative sessions. In the postoperative period, an eye mask and ear plug will be applied to the patient by the researcher on the 3rd and 4th days of the short CBT post-op and between 23:00 and 07:00 at night. Visual Analogue Scale, State Anxiety Inventory, Richmond Agitation-Sedation Scale, Confusion Evaluation Scale in Intensive Care, Richard Campbell Sleep Quality Scale, Daily Follow-up Form will be applied after open heart surgery.
Psychosocial nursing intervention
The sessions were planned to be at least 45 minutes in a time suitable for the groups, with the bed curtains drawn if possible. Session 1: The purpose of this session; Brief CIS information will be provided. Session 2: The session starts with mood control of individuals. It is discussed whether they have experienced an event that occupies their minds and is likely to affect their illness. Session 3: It starts with mood control of individuals. They are asked if there is anything from the places where the guests are. Cognitive reviews are reviewed. It aims to describe recent stressful observations, negative automatic outcome descriptions, and evaluation of such experiences. 4.Session: The session starts with the mood control of the patient. It is discussed whether the patient has experienced an event that occupies his mind. Continuous analysis of negative thoughts and review of cognitive techniques and coping mechanisms are provided.
Control
Patients who meet the research criteria and agree to participate in the study will be informed about the research process (purpose of the research, assignment to the intervention and control group, etc.), written informed consent and contact information of the patients will be obtained, and the contact information of the researcher will be given to the patient. Only routine nursing care will be given to the patient. will be applied by the researcher
No interventions assigned to this group
Interventions
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Psychosocial nursing intervention
The sessions were planned to be at least 45 minutes in a time suitable for the groups, with the bed curtains drawn if possible. Session 1: The purpose of this session; Brief CIS information will be provided. Session 2: The session starts with mood control of individuals. It is discussed whether they have experienced an event that occupies their minds and is likely to affect their illness. Session 3: It starts with mood control of individuals. They are asked if there is anything from the places where the guests are. Cognitive reviews are reviewed. It aims to describe recent stressful observations, negative automatic outcome descriptions, and evaluation of such experiences. 4.Session: The session starts with the mood control of the patient. It is discussed whether the patient has experienced an event that occupies his mind. Continuous analysis of negative thoughts and review of cognitive techniques and coping mechanisms are provided.
Eligibility Criteria
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Inclusion Criteria
* over the age of 18,
* Patients who will undergo open heart surgery for the first time,
* Not diagnosed with any psychiatric disease,
* Conscious, cooperative, hemodynamically stable (blood pressure not below 70/50mHg), not on mechanical ventilator
* Patients with a state anxiety scale score of 40 and above,
* Low and medium risk patients evaluated with the European System for Cardiac Operative Risk Evaluation (EuroSkor), the risk scoring system used to predict mortality in the preoperative period in cardiac surgery,
* Literate, with sufficient communication skills and Turkish-speaking
* Those who signed the Informed Consent Form to participate in the study will be included.
Exclusion Criteria
* Emergency patients for whom open heart surgery has not been planned before,
* Diagnosed with dementia,
* Standardized mini mental test (SMMT) below 3 points,
* Has a history of previous cerebrovascular accident (CVO),
* Severe comorbidity
* Patients with a high EuroScore and prolonged mechanical ventilator duration
* Those who do not sign the Informed Consent Form to participate in the study will not be included.
18 Years
75 Years
ALL
Yes
Sponsors
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Mersin University
OTHER
Responsible Party
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FİRDEVS EBRU ÖZDEMİR
Specialist Nurse
Principal Investigators
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Mualla YILMAZ, PhD
Role: STUDY_DIRECTOR
Prof. Dr.
Locations
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Firdevs Ebru ÖZDEMİR
Mersin, Yenişehir, Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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Interventional
Identifier Type: -
Identifier Source: org_study_id
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