MedTrace Logo

Effect of Comic-Based Education on Attitudes Toward Patient Rights

NCT07772999 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 76

Last updated 2026-08-19

No results posted yet for this study

Summary

The goal of this randomized controlled trial is to evaluate whether comic-based education improves attitudes toward the use of patient rights among adults receiving inpatient care. The main question is whether patients who receive comic-based patient rights education have more positive attitudes toward using their patient rights than patients who receive routine verbal and written patient rights education.

Participants will be randomly assigned to one of two groups. The intervention group will receive an approximately 15-minute, individual, face-to-face patient rights education session using a comic-based educational brochure. The control group will receive the hospital's routine patient rights education, consisting of verbal and written information provided by clinical nurses for approximately 15 minutes. Attitudes toward the use of patient rights will be measured before and immediately after the education in both groups.

Conditions

  • Patient Rights

Interventions

BEHAVIORAL

Comic-Based Patient Rights Education

Participants will receive a single, individual, face-to-face patient rights education session using a comic-based educational brochure developed in accordance with the Turkish Patient Rights Regulation. The education will be delivered by the researcher and will last approximately 15 minutes. The brochure presents patient rights through visual narratives and short patient-nurse dialogues and will be provided to the participant after the education.

BEHAVIORAL

Routine Patient Rights Education

Participants will receive the hospital's routine patient rights education provided individually by clinical nurses. The education will consist of verbal information supported by the institution's standard written educational materials and will last approximately 15 minutes.

Sponsors & Collaborators

  • Abant Izzet Baysal University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-09-01
Primary Completion
2026-09-30
Completion
2026-10-30

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07772999 on ClinicalTrials.gov