Breaking the Bad News to the Bereaved Family and Their Reactions

NCT ID: NCT04385628

Last Updated: 2020-05-13

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

UNKNOWN

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-04-25

Study Completion Date

2020-11-30

Brief Summary

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The demographic characteristics, satisfaction survey evaluations and emotional reactions of the relatives of the patients who are admitted to the intensive care unit and who have an expected mortality rate higher than 50% according to the Apache-2 scoring system will be investigated.

Detailed Description

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Patients with an APACHE-2 score\> 25 (Expected mortality rate\> 50%) during the first 24 hours of hospitalization in the Intensive Care Unit will be included in the study. A person who comes to the most frequent visit from relatives of patients will be included in the study. Demographic data of the relative of the patient after the informed volunteer consent form has been approved (age, proximity, educational background, patient co-existence, ethnicity, marital status, number of children, history of psychological treatment and the presence of an intensive care treatment history of any family member before) will be registered. After the 3rd, 10th, and 30th days of patient admission, and once a month, the patient satisfaction survey will be filled face to face during informing the patient's relative. In this patient group with an expected mortality of\> 50%, if death occurs, the information will be made to the visitor of the patient who frequently visits the patient and agrees to participate in the study. The emotional reaction of the relative of the patient participating in the study during the declaration of death will be recorded in the case report form.

Grief reaction is unique, and it will differ from one individual to another. Possible reactions of relatives of patients during the death notification (Emotional Reactions)

1. Regular response; In this case, the relatives of the patients often describe the event as expected or my patient is now free from suffering.
2. Initial shock reaction; It may be complete desperation and a state of closure,
3. Denial- This is an initial defense mechanism after the unexpected, devastating news, and it should be recognized and tolerated. Acceptance may be possible by encouraging the relatives to view the body of the deceased, especially to those relatives who were not present at the time of death
4. Anger- This is a common reaction after the sudden death of a beloved relative. The expression of this anger can vary from mild irritation to violent behavior. This can be expressed on self, hospital staff, or any other person. Anger will gradually diminish once expressed
5. Guilt- This is nothing but the inward expression of anger and self-blame. Consoling words of the health care team will help to do away with this emotion.

Conditions

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The Effective Factors on the Grief Reactions to the Death Information

Study Design

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Observational Model Type

FAMILY_BASED

Study Time Perspective

PROSPECTIVE

Study Groups

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Relatives of patients hospitalized in the intensive care unit

Demographic data of the relative of the patient (age, proximity, educational background, patient co-existence, ethnicity, marital status, number of children, history of psychological treatment and the presence of an intensive care treatment history of any family member before) will be recorded. After the 3rd, 10th, and 30th days of patient admission, and once a month, the patient satisfaction survey will be filled face to face during informing the patient's relative. These three main data (Demographic data of the patient relatives, the most recent satisfaction questionnaire and emotional reactions observed while reporting death) will be evaluated and interpreted.

the patient' relatives satisfaction questionnaire

Intervention Type BEHAVIORAL

The patient' relatives satisfaction questionnaire will be filled face to face during informing the patient's relatives after the 3rd, 10th, and 30th days of patient admission, and once a month. We will evaluate the most recent questionnaire.

Interventions

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the patient' relatives satisfaction questionnaire

The patient' relatives satisfaction questionnaire will be filled face to face during informing the patient's relatives after the 3rd, 10th, and 30th days of patient admission, and once a month. We will evaluate the most recent questionnaire.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Apache 2 score\> 25 or Expected death rate\> 50%,
* Hospitalization period\> 72 hours in intensive care unit -

Exclusion Criteria

* Apache 2 score \<25 or Expected death rate \<50%,
* Those who have a stay in ICU \<72 hours
* Currently receiving psychological medication
* Those who do not accept one of the legal heirs to participate in the study
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Sultan Abdulhamid Han Training and Research Hospital, Istanbul, Turkey

OTHER

Sponsor Role lead

Responsible Party

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Bülent Barış Güven

medical doctor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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selçuk Taşçı

Role: STUDY_CHAIR

Sultan Abdulhamidhan Training Hospital

ayşın ersoy

Role: STUDY_DIRECTOR

Sultan Abdulhamidhan Training Hospital

Locations

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Sultan 2.Abdulhamidhan training hospital

Istanbul, , Turkey (Türkiye)

Site Status RECRUITING

Countries

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Turkey (Türkiye)

Central Contacts

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bülent barış güven

Role: CONTACT

05336383445

selçuk Taşçı

Role: CONTACT

05359715480

Facility Contacts

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Bülent B güven

Role: primary

05336383445

References

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Naik SB. Death in the hospital: Breaking the bad news to the bereaved family. Indian J Crit Care Med. 2013 May;17(3):178-81. doi: 10.4103/0972-5229.117067.

Reference Type RESULT
PMID: 24082616 (View on PubMed)

Jurkovich GJ, Pierce B, Pananen L, Rivara FP. Giving bad news: the family perspective. J Trauma. 2000 May;48(5):865-70; discussion 870-3. doi: 10.1097/00005373-200005000-00009.

Reference Type RESULT
PMID: 10823529 (View on PubMed)

Other Identifiers

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48670771-514.10

Identifier Type: -

Identifier Source: org_study_id

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