📚 Basics of Clinical Trials
For beginners and students new to clinical research
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What are clinical trials?
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Phases of clinical trials (Phase I-IV)
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Key terms and definitions (e.g., placebo, blinding, randomization)
2. 📝 Study Design & Protocols
Discuss trial methodology and protocol structure
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How to write a clinical trial protocol
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Choosing study populations
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Randomized controlled trials vs. observational studies
3. ⚖️ Ethics & Regulations
Discussion of ethical concerns, informed consent, and IRB processes
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Good Clinical Practice (GCP) guidelines
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Informed consent templates
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Regulatory bodies (FDA, EMA, NIH, etc.)
4. 📊 Data Collection & Analysis
For sharing tips and queries about data handling in trials
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How to record and manage trial data
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Data monitoring and safety committees
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Statistical analysis in clinical trials
5. 🌍 Global Trials & Registries
Talk about multicenter and international trials
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How to register a trial (e.g., ClinicalTrials.gov)
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Challenges in global coordination
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Language/cultural barriers in trial design
6. 💬 Ongoing & Completed Trials
Share or ask about current or past clinical trials
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Showcase your trial/study
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Ask for collaborators
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Seek participants (where appropriate)
7. ❓ Q&A / Troubleshooting
For questions and help with clinical trial-related problems
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Issues with IRB submissions
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Recruitment challenges
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Site management problems
8. 🧠 AI in Clinical Trials
Explore how artificial intelligence is transforming clinical trials
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Predictive analytics in patient recruitment
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Automating protocol adherence
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Real-time monitoring using AI tools