Breast Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have a confirmed diagnosis of breast cancer at stage I, II, or III
- People who are about to start their very first round of chemotherapy
- People who are 18 years of age or older
- People who are able to understand the study and agree to take part by signing a consent form
- People who own a smartphone (Android or Apple) and are comfortable using mobile apps, reading on-screen text in Arabic, and entering daily health information into an app (this applies to the active treatment group)
- People who are willing to follow the study's procedures and attend follow-up appointments
- People who are able to communicate in Arabic, as the app and chatbot used in this study are in Arabic
Who may not be able to join:
- People who have stage IV (metastatic) breast cancer, meaning cancer that has spread to other parts of the body
- People who are receiving hormonal therapy at the same time as chemotherapy during the study period
- People who have significant memory, thinking, or severe mental health difficulties that would make it hard to use the mobile app or complete questionnaires (confirm with trial site)
- People who are receiving palliative (comfort-focused) care only, where chemotherapy is not being given with the goal of treating or extending life
- People who are already taking part in another clinical trial that involves a treatment or intervention
- People who have serious other health conditions that could significantly affect their ability to take part or influence the study results (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Samer Imad Mohammed, Assistant Prof, University of Baghdad-College of Pharmacy
Phone: +9647901572647
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in Symptom Burden and Chemotherapy-Related Toxicities (Arabic PRO-CTCAE); Medication Adherence Score (Arabic MMAS-8; Change in Patient Knowledge and Information Satisfaction (EORTC QLQ-INFO25); Change in General Quality of Life (EORTC QLQ-C30); Change in Breast Cancer-Specific Quality of Life (EORTC QLQ-BR23)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.