Family Support Weaning from Mechanical Ventilation in Cardiovascular Surgery

NCT ID: NCT05820789

Last Updated: 2025-03-06

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-04-30

Study Completion Date

2024-04-20

Brief Summary

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Mechanical ventilation support is used to ensure airway clarity in patients after surgery.If patients are not informed about mechanical ventilation treatment in the pre -operation period, panic, anxiety and comfort may be experienced when they wake up from anesthesia and find them in intensive care under mechanical ventilation with various tubes and equipment. The separation from the mechanical ventilator (MV) covers the patient's mechanical support and the entire process of separation of endotrakeal tube.During the separation of the mechanical ventilator, the support of one of the patient members of the patient may increase the stress and comfort of the patient. Therefore, this research is planned

Detailed Description

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Intensive care nurses spend a long time with patients and observe them closely. Intensive care nurses in the MV separation process; plays a special and important role. Recently, family support has been used in patient care. An increase in anxiety and comfort levels is observed in patients receiving family support. This study was planned with the aim of supporting the patient by the family member during the separation of the patient from the mechanical ventilator after cardiac surgery and to evaluate the comfort and anxiety level of the patients.

Conditions

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Patient Comfort Anxiety Patient Satisfaction

Study Design

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Allocation Method

NA

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Experimental Group

When the patient comes intubated from the surgery to the cardiovascular surgery intensive care unit, when they meet the extubation criteria, the patients will be extubated by the healthcare professionals working in the intensive care unit in accordance with the service protocol.Patients in the experimental group will be provided with their relatives and support during weaning from the mechanical ventilator.

Group Type EXPERIMENTAL

Family support

Intervention Type OTHER

Before the extubation procedure, the patient's relatives will be informed, and the patient will be allowed to enter the intensive care unit, and the patient will be able to express that he is with the patient by holding his hand and talking.

Control Group

Patient comes intubated from the surgery to the cardiovascular surgery intensive care unit, when they meet the extubation criteria, the patients will be extubated by the healthcare professionals working in the intensive care unit in accordance with the service protocol.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Family support

Before the extubation procedure, the patient's relatives will be informed, and the patient will be allowed to enter the intensive care unit, and the patient will be able to express that he is with the patient by holding his hand and talking.

Intervention Type OTHER

Other Intervention Names

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Experimantal group

Eligibility Criteria

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Inclusion Criteria

* Volunteering to participate in the research
* To agree to participate in the research verbally and in writing
* To be over the age of 18
* Knowing Turkish
* Not having any psychiatric disease
* No vision, hearing and perception problems
* Receiving mechanical ventilator support after cardiac surgery and being followed in the intensive care unit.

* Other patients receiving mechanical ventilator support after surgery in the intensive care unit other than cardiac surgery
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kastamonu University

OTHER

Sponsor Role lead

Responsible Party

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Selda Karaveli Çakır

Assistant professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Selda Karaveli Cakir

Role: PRINCIPAL_INVESTIGATOR

Kastamonu Universty

Locations

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Kastamonu University

Kastamonu, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2022-KAEK-146

Identifier Type: -

Identifier Source: org_study_id

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