← Back to Home1. Study Information
Study Title:
[Enter study title]
Principal Investigator:
[Name, credentials]
Study Dates:
[Start date] - [End date]
IRB Protocol Number:
[IRB #]
2. Research Question & Hypothesis
Primary Research Question
[State your primary research question]
Hypothesis
H0: [Null hypothesis]
H1: [Alternative hypothesis]
Secondary Objectives
• [Secondary objective 1]
• [Secondary objective 2]
• [Secondary objective 3]
3. Study Design
Study Type: [ ] In vitro [ ] Ex vivo [ ] Clinical [ ] Observational
Experimental Groups:
Control Group: [Description]
Treatment Group 1: [Description]
Treatment Group 2: [Description]
Sample Size Calculation:
Power: [e.g., 80%]
Alpha: [e.g., 0.05]
Effect size: [Expected difference]
Required n per group: [Number]
4. Methods
4.1 Materials
Cell lines: [Specify]
Reagents: [List with catalog numbers]
Equipment: [List]
4.2 Procedures
Step 1: [Detailed procedure]
Step 2: [Detailed procedure]
Step 3: [Detailed procedure]
4.3 Outcome Measures
Primary endpoint: [What you're measuring]
Secondary endpoints: [Additional measurements]
Timepoints: [When measurements occur]
5. Data Analysis Plan
Statistical Tests:
[Specify tests for each comparison]
Software:
[Prism, R, Python, etc.]
Significance Level: α = 0.05 (two-tailed)
6. Timeline
Week 1-2: [Activity]
Week 3-4: [Activity]
Week 5-6: [Activity]
Week 7-8: [Data analysis]
7. References
[1] Citation
[2] Citation
[3] Citation