Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT06796166

The Impact of AI- Supported Education in Mastectomy Patient

Led by Bezmialem Vakif University · Updated on 2025-01-30

40

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

Sponsors

B

Bezmialem Vakif University

Lead Sponsor

A

Acibadem University

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study aims to evaluate the impact of artificial intelligence (AI)-supported preoperative education on fear and anxiety levels in patients undergoing total mastectomy. It is a randomized controlled trial involving two groups: one receiving AI-supported education and the other receiving standard preoperative education. The primary outcomes are to assess changes in surgical fear and anxiety levels. The study targets adult female patients diagnosed with breast cancer who are scheduled for total mastectomy.

CONDITIONS

Official Title

The Impact of AI- Supported Education in Mastectomy Patient

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Literate female patients
  • Patients who will undergo total mastectomy surgery
  • Patients diagnosed with breast cancer
  • Patients who are over 18 years of age
  • Patients who agree to participate and provide written consent
Not Eligible

You will not qualify if you...

  • Patients who cannot understand or communicate in Turkish
  • Patients with active psychiatric disorders such as major depression, bipolar disorder, or schizophrenia
  • Patients with advanced hearing or vision problems
  • Patients with mental disabilities
  • Patients who have previously participated in a similar training program

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Acibadem International Hospital

Istanbul, Bakirköy, Turkey (Türkiye), 34149

Actively Recruiting

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Research Team

M

Mahmut DAĞCI, PhD

CONTACT

G

Gamze ORHAN, M. Sc.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

2

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