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NCT07452055: EMBRACE

Large Language Model-Based Emotional Management for Breast Cancer Patients

Not yet recruiting NA Last updated 12 March 2026
What this trial tests

NA trial testing Large Language Model-Based precision emotional intervention system in Primary Breast Cancer in 440 participants. Not yet recruiting.

Timeline
10 March 2026
Primary endpoint
1 October 2026
1 November 2026

Quick facts

Lead sponsorNanfang Hospital, Southern Medical University
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingsingle
Primary purposesupportive care
Enrollment440
Start date10 March 2026
Primary completion1 October 2026
Estimated completion1 November 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Nanfang Hospital, Southern Medical University

Who can join

18 and older, any sex, with Primary Breast Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study (study type: randomized controlled trial) aims to evaluate whether a large language model-based precision emotional management intervention can improve health-related quality of life among patients with primary breast cancer. The study will enroll adult women (≥18 years old) with pathologically confirmed primary breast cancer who own a smartphone, regularly use social media platforms, and have an expected survival of at least 6 months. The primary questions this study seeks to answer are: 1. Does the intervention improve health-related quality of life (EORTC QLQ-C30 summary score) at 6 months post-intervention? 2. Does the intervention reduce anxiety, depression, cancer-related symptom burden, and unplanned hospitalizations in this population? With a control group in place, researchers will compare changes in health-related quality of life, anxiety, depression, and cancer-related symptom burden between the intervention group (receiving digital precision emotional management plus usual care) and the control group (receiving usual care only) to determine whether the intervention leads to significant improvements in these outcomes. Participants will be required to: 1. Complete baseline and follow-up assessments of health-related quality of life, anxiety, depression, and cancer-related symptoms at 1, 3, and 6 months post-randomization. 2. For those in the intervention group, use the digital precision emotional management system autonomously for 6 months, including submitting self-reported emotional diaries and completing biweekly skill translation assessments. 3. For all participants, report any adverse events and unplanned hospitalizations during the study period.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other Nanfang Hospital, Southern Medical University trials

Trials by the same sponsor.

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