Effect of Informing Family Members of Patients During Surgery
NCT ID: NCT06723600
Last Updated: 2024-12-09
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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RECRUITING
NA
104 participants
INTERVENTIONAL
2024-06-10
2025-05-10
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
DOUBLE
Study Groups
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Experimental Group
The experimental group relatives of patients will be informed by the nurse during surgery.
Information
Nurse-led family member information
Control Group
The control group will take rutin informing.
No interventions assigned to this group
Interventions
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Information
Nurse-led family member information
Eligibility Criteria
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Inclusion Criteria
* Being able to understand and speak Turkish,
* Being literate,
* Willing to participate in the study,
* Using a phone,
* Being present in the hospital before, during, and after the surgery.
Exclusion Criteria
* Having a psychiatric disorder or using psychiatric medication.
Endpoint Criteria:
* Inability to reach the participant when called during the surgery,
* The patient's death during the surgery.
18 Years
ALL
Yes
Sponsors
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Karadeniz Technical University
OTHER
Responsible Party
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Bahar CANDAS ALTINBAS
Assistant Professor
Principal Investigators
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Bahar Candas Altinbas
Role: PRINCIPAL_INVESTIGATOR
Karadeniz Technical University
Locations
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Karadeniz Technical University
Trabzon, Milli Egemenlik, Turkey (Türkiye)
Countries
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Central Contacts
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Facility Contacts
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Bahar Candas Altinbas, PhD
Role: primary
Other Identifiers
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Nurse_Anxiety
Identifier Type: -
Identifier Source: org_study_id