AI-based Skeleton Recognition System for Rehabilitation Exercise in Breast Cancer Survivors: A Randomized Controlled Trial
Launched by FUDAN UNIVERSITY · Oct 14, 2024
Trial Information
Current as of July 09, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a new technology that uses artificial intelligence (AI) to help breast cancer survivors who are experiencing muscle and joint pain due to a type of hormone therapy called aromatase inhibitors. The aim is to create a special program that supports patients in doing rehabilitation exercises at home, making it easier for them to stay active and improve their quality of life. By using AI, the system will be able to provide real-time feedback during exercises, ensuring that participants engage in appropriate movements tailored to their needs.
To be eligible for the trial, participants must have been diagnosed with hormone receptor-positive breast cancer and be currently receiving aromatase inhibitors. They should also be postmenopausal and experiencing some level of bone or joint pain. Importantly, those interested in joining the study should not be involved in other physical therapy or exercise programs that could interfere with the trial. Participants will have the opportunity to engage in a personalized exercise regimen that may help alleviate their symptoms while being monitored and supported by the AI system. This innovative approach aims to make rehabilitation more accessible and effective for breast cancer survivors.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Pathologically confirmed hormone receptor-positive breast cancer (stage I, II, III).
- • 2. Initiation of treatment with aromatase inhibitors (e.g., anastrozole, letrozole, exemestane).
- • 3. Postmenopausal women, including those with surgically induced menopause. 4. Clear consciousness, no cognitive or communication impairments, and able to comply with the intervention.
- • 5. Informed consent obtained, with voluntary participation in the study. 6. Bone and joint symptoms with a Brief Pain Inventory (BPI) score of ≥3, or presence of at least one of the following risk factors: elevated bone turnover markers, reduced vitamin D levels, increased inflammatory cytokines, elevated C-reactive protein, or elevated rheumatoid factor.
- • 7. Not participating in any physical therapy or exercise-based interventions that may interfere with this study.
- Exclusion Criteria:
- • - 1. Recurrence of breast cancer or distant metastasis. 2. Presence of other malignancies. 3. Diagnosed rheumatoid arthritis, bone and joint trauma, or other severe bone and joint diseases.
- • 4. Bone mineral density T-score \<-2.5. 5. Presence of absolute contraindications to exercise.
About Fudan University
Fudan University, a prestigious comprehensive research university located in Shanghai, China, is committed to advancing medical science through innovative clinical research. Renowned for its rigorous academic standards and cutting-edge research facilities, Fudan University plays a pivotal role in the global health landscape by sponsoring a diverse array of clinical trials aimed at improving patient outcomes and addressing pressing medical challenges. Leveraging its multidisciplinary expertise and collaborative networks, the university strives to translate scientific discoveries into practical applications, fostering advancements in healthcare and contributing to the well-being of communities both locally and internationally.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Shanghai, , China
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported