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Starting soon Not applicable

Reflects the Intervention (AI Chatbot)

NCT06943911 · tracked via the Priya Life Science Egypt tracker
Sponsor
Mostafa Shaban
Phase
Not applicable
Started
2025-04-20
Last updated
2025-04-25

Condition(s) studied

Breast Cancer Early Stage Breast Cancer (Stage 1-3)

Investigational drug(s) / intervention(s)

AI Chatbot for Breast Cancer Patient Education and Empowerment

AI Chatbot for Breast Cancer Patient Education and Empowerment: The AI Chatbot for Breast Cancer Patient Education and Empowerment is a digital health intervention that leverages artificial intelligence to provide personalized educational content and emotional support to breast cancer patients. The chatbot delivers information on breast cancer management, treatment options, side effects, and self-care practices. It is available 24/7, offering real-time answers to patient queries and tailored suggestions based on their treatment path. The aim is to increase patient knowledge, improve attitudes toward AI, and empower patients to take a more active role in their care. The chatbot intervention is provided alongside standard oncology care at Kafr El-Sheikh University Hospital.

Study summary

The goal of this clinical trial is to investigate the impact of an AI-powered chatbot intervention on improving knowledge, attitudes, and empowerment in breast cancer patients. The study focuses on female breast cancer patients, aged 18 years or older, who are receiving treatment at Kafr El-Sheikh University Hospital in Egypt.

The main questions it aims to answer are:

Can the AI chatbot intervention improve breast cancer knowledge compared to standard care?

Can the AI chatbot intervention positively influence attitudes toward AI in healthcare?

Does the AI chatbot intervention enhance patient empowerment in managing breast cancer?

Researchers will compare:

Intervention group (AI chatbot + standard care) to control group (standard care alone) to see if the AI chatbot intervention leads to greater improvements in knowledge, more positive attitudes towards AI, and higher perceived empowerment.

Participants will:

Engage with an AI-powered chatbot designed to provide personalized education on breast cancer, treatment options, and emotional support.

Complete pre- and post-intervention assessments to measure changes in knowledge, attitudes toward AI, and empowerment.

Receive standard care, including routine oncology consultations and nursing support, alongside the chatbot intervention (for the intervention group).

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria: Female participants diagnosed with breast cancer, regardless of cancer stage. Age 18 years or older. Ability to read and communicate in Arabic to interact with the AI chatbot. Willingness to participate in the study and to engage with the AI chatbot for the duration of the intervention. Ability to provide informed consent. Exclusion Criteria: Participants with cognitive impairments or serious mental health conditions that may hinder understanding or participation in the study. Patients currently receiving palliative care, as they may prioritize symptom management over educational interventions. Participants who are physically unable to engage with the study's digital tools or complete assessments (e.g., due to severe illness). Individuals who are unable to communicate in Arabic, as the AI chatbot intervention is designed in Arabic.

Primary outcome measure(s)

  • Breast Cancer Knowledge Improvement — 2 months
    This outcome measures the change in breast cancer knowledge from baseline to post-intervention for participants who used the AI chatbot compared to the control group. Knowledge is assessed using the Artificial Intelligence of Breast Cancer Questionnaire, which covers topics such as treatment options, side effects, symptom management, and AI's role in healthcare.

Trial sites (1)

FacilityCityRegionStatus
Faculty of Nursing Cairo University Cairo Egypt
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06943911 on ClinicalTrials.gov ↗ ← All trials in Egypt