Actively Recruiting
The Impact of Social Media-Delivered Chemotherapy Side Effects Education for Breast Cancer Patients Receiving First-Time Chemotherapy
Led by Taipei Medical University Shuang Ho Hospital · Updated on 2025-01-24
100
Participants Needed
1
Research Sites
55 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating whether a standardized education program delivered by pharmacists through social media can improve breast cancer patients' knowledge about chemotherapy side effects. The study compares two methods: an education video plus standard information versus traditional chemotherapy handouts. This trial focuses on patients receiving their first chemotherapy treatment. Participants are randomly assigned to either watch a pharmacist-provided educational video during their chemotherapy visits and have ongoing access to it throughout their treatment, or receive brief pharmacist explanations along with chemotherapy handouts. The video covers side effect mechanisms, recognition, prevention, non-medical management, and instructions on when to seek hospital care. The video session lasts 15 to 20 minutes, while the handout explanation takes about 5 to 10 minutes. During the study, participants complete questionnaires assessing their knowledge and quality of life before and after receiving education at both the first and second chemotherapy sessions. The main outcome is measured by a 5-question side effects management questionnaire administered at these two time points. This helps researchers understand the impact of the educational methods on patient knowledge and management of chemotherapy side effects.
CONDITIONS
Official Title
The Impact of Social Media-delivered Chemotherapy Side Effects Education for Breast Cancer Patients Receiving Chemotherapy
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Breast cancer patients aged 18 or older undergoing their first chemotherapy.
- Possess a smartphone and are able to watch videos on it.
You will not qualify if you...
- Unable to read or complete questionnaires in Chinese.
- Cognitive impairments.
- Pregnant women.
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Trial Site Locations
Total: 1 location
1
Shuang Ho Hospital
New Taipei City, Taiwan
Actively Recruiting
Research Team
P
Pohung Lin, PharmD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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