RecruitingNot Applicable

The Impact of AI- Supported Education in Mastectomy Patient

Turkey (Türkiye)40 participantsStarted 2024-08-01

Plain-language summary

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.

Who can participate

Age range18 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria: * 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 in the study and from whom written consent has been obtained will be included in the study. Exclusion criteria: * Patients who cannot understand or communicate in Turkish * Patients with active psychiatric disorders (e.g., major depression, bipolar disorder, schizophrenia) * Patients with advanced hearing or vision problems * Patients with mental disabilities * Patients who have previously participated in a similar training program will be excluded from the study.

What they're measuring

Surgical Fear Questionnaire / SFQ

Timeframe: The scales will be administered twice: 15 minutes before the preoperative education session and 15 minutes after the preoperative education session.

State-Trait Anxiety Inventory /STAI

Timeframe: The scales will be administered twice: 15 minutes before the preoperative education session and 15 minutes after the preoperative education session.

Trial details

NCT IDNCT06796166

SponsorBezmialem Vakif University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-02-01

Contact for this trial

Mahmut DAĞCI, PhD

+90 05547618939 MDagci@bezmialem.edu.tr

View on ClinicalTrials.gov More Breast Cancer trials

Plain-language summary

Who can participate

Age range18 Years

SexFEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Surgical Fear Questionnaire / SFQ

Timeframe: The scales will be administered twice: 15 minutes before the preoperative education session and 15 minutes after the preoperative education session.

State-Trait Anxiety Inventory /STAI

Timeframe: The scales will be administered twice: 15 minutes before the preoperative education session and 15 minutes after the preoperative education session.