Actively Recruiting
The Impact of Respiratory Training of DIBH Radiotherapy for Breast Cancer
Led by Jianjun Lai · Updated on 2024-07-05
80
Participants Needed
1
Research Sites
110 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Breast cancer DIBH (Deep Inspiration Breath Hold) radiotherapy represents a high-precision treatment approach that substantially minimizes radiation exposure to vital organs such as the heart, thus enhancing protection of the patient's heart, lungs, contralateral breast, and other normal tissues compared to conventional radiotherapy techniques. This method requires meticulous precision, necessitating that patients possess exceptional respiratory control, which is facilitated through specialized equipment. Without such control, patients may encounter issues like missed targets, significant setup errors, and extended treatment durations. In this study, the research team employed portable devices to enable patients to independently perform daily respiratory training exercises. The control group received no such devices; instead, these patients were merely instructed verbally on the importance of improving their breath-holding capabilities. The effectiveness of this intervention was evaluated by comparing the daily setup errors between the two groups. Additionally, the intervention's influence on patient outcomes was assessed by monitoring the toxicity and side effects experienced by the patients.
CONDITIONS
Official Title
The Impact of Respiratory Training of DIBH Radiotherapy for Breast Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Breast cancer radiotherapy patients
- Able to hold a single breath for more than 10 seconds
You will not qualify if you...
- Unable to hold a single breath for more than 10 seconds
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Zhejiang Hospital
Hangzhou, Zhejiang, China
Actively Recruiting
Research Team
J
Jianjun Lai
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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