ClinicalTrials.Veeva

Menu

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

B

Bahçeşehir University

Status

Terminated

Conditions

Intracranial Surgery

Treatments

Other: discharge training (oral and written brochure)
Other: discharge education (oral education)

Study type

Interventional

Funder types

Other

Identifiers

NCT07012681
Caygor/08.05.2025

Details and patient eligibility

About

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.

Full description

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.

Enrollment

40 patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

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

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

40 participants in 2 patient groups

discharge education (oral education)
Experimental group
Description:
oral training group
Treatment:
Other: discharge education (oral education)
discharge training (oral and written training)
Experimental group
Description:
The group that received oral and written brochure training
Treatment:
Other: discharge training (oral and written brochure)

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems