Investigation of the Effects of Discharge Education Strategies on Quality of Life and Daily Living Activities in Patients Who Have Undergone Intracranial Surgery.

NCT ID: NCT07012681

Last Updated: 2025-06-10

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

TERMINATED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-10-15

Study Completion Date

2025-05-09

Brief Summary

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It was planned to provide education using verbal education or verbal and picture-text brochure method as a discharge education strategy for patients who underwent intracranial surgery. In this context, it was aimed to compare the effects of two discharge education strategies used in the discharge education of patients who underwent intracranial surgery on the quality of life and daily living activities of the patients.

Detailed Description

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In this study, it was planned to provide education to patients who underwent intracranial surgery by using verbal education or verbal and pictorial brochure methods as a discharge education strategy. The evaluation of the effect of this education, which includes content on skin wound care, nutrition, drainage, exercise, medication management and seizures, on the quality of life and daily living activities of the patients In this context, it was aimed to compare the effects of two discharge education strategies used in the discharge education of patients who underwent intracranial surgery on the quality of life and daily living activities of the patients.

Conditions

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Intracranial Surgery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Arm 1: Oral Training Group Arm 2: Oral and Written Brochure training Group
Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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discharge education (oral education)

oral training group

Group Type EXPERIMENTAL

discharge education (oral education)

Intervention Type OTHER

group receiving oral training in discharge training

discharge training (oral and written training)

The group that received oral and written brochure training

Group Type EXPERIMENTAL

discharge training (oral and written brochure)

Intervention Type OTHER

The group that received oral and written brochure training during discharge training

Interventions

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discharge training (oral and written brochure)

The group that received oral and written brochure training during discharge training

Intervention Type OTHER

discharge education (oral education)

group receiving oral training in discharge training

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

Participants must meet all of the following criteria:

* Have undergone intracranial surgery
* Voluntarily agree to participate in the study
* Be between 18 and 75 years of age
* Be literate and speak Turkish
* Be open to communication and cooperation
* Be mentally healthy
* Have no visual, hearing, or speech impairments

Exclusion Criteria

Participants will be excluded from the study if they meet any of the following:

* Refuse to participate in the study
* Are not native Turkish speakers
* Are illiterate
* Have visual, hearing, or speech impairments
* Have a diagnosed psychological disorder
* Have been diagnosed with dementia or Alzheimer's disease
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Bahçeşehir University

OTHER

Sponsor Role lead

Responsible Party

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Hanife Damla Çaygör

Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Haseki Eğitim ve Araştırma Hastanesi

Istanbul, Sultangazi, Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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Caygor/08.05.2025

Identifier Type: -

Identifier Source: org_study_id

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