Monitoring recovery after breast surgery using wearable technology
Breast: Recovery After Axillary Node Clearance - Evaluating Limbs With E-Technology (the BRACELET Study)
Imperial College London · NCT03635723
This study tests how wearable sensors can help track the recovery of physical activity in patients after breast surgery to better understand their healing process.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 75 (estimated) |
| Sex | All |
| Sponsor | Imperial College London (other) |
| Locations | 1 site (London) |
| Trial ID | NCT03635723 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the recovery of physical activity in patients who have undergone breast or axillary surgery by utilizing wearable sensors. These sensors will objectively measure activity levels and arm movements, providing more accurate data than traditional patient self-reports. The focus is on understanding how patients return to normal physical activity post-surgery, which can inform rehabilitation practices. The observational nature of the study allows for real-time data collection without intervention.
Who should consider this trial
Good fit: Ideal candidates are individuals who have recently undergone breast or axillary surgery.
Not a fit: Patients with other diagnosed movement disorders or those unable to consent due to language or capacity issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance rehabilitation strategies for breast cancer patients, leading to improved recovery outcomes.
How similar studies have performed: Other studies utilizing wearable technology for monitoring recovery have shown promising results, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Breast or axillary surgery Exclusion Criteria: * Other diagnosed movement disorder * Cannot consent due to language or capacity
Where this trial is running
London
- Imperial College Healthcare NHS Trust — London, United Kingdom (RECRUITING)
Study contacts
- Principal investigator: Richard Kwasnicki — Imperial College London
- Study coordinator: Richard M Kwasnicki, PhD MRCS
- Email: rmk107@ic.ac.uk
- Phone: +44 (0) 20 759 48904
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.
Conditions: Breast Cancer, Mobility Limitation, Technology, Rehabilitation, Wearables, Breast surgery, Physical activity, Enhanced recovery after surgery