Study Protocol Planner
A ready-to-run research protocol from one question: design, sample size with its math, tasks or endpoints, timeline, bias risks, analysis plan and ethics checklist.
Built for researchers, product teams and analysts planning a research protocol before collecting data.
Why this work is hard
Researchers, product teams and analysts planning a study before collecting data spend hours on this by hand: finding the right sources, reading them, checking them against each other and writing up what matters. The work is repetitive, it is easy to miss something, and nobody can show where a claim came from.
Study Protocol Planner does that work as a GREP AI agent. It runs when you ask, and you can put it on a daily, weekly or monthly schedule. Every run delivers a sourced report, with every claim linked to its source.
What you get
What Study Protocol Planner delivers
FAQ
What does Study Protocol Planner need to run?
Study Protocol Planner needs research question or hypothesis; method and participants (optional), constraints: time, budget, tools, rules (optional) and field or setting (optional) are optional.
How often does Study Protocol Planner run?
It runs when you ask, and you can put it on a daily, weekly or monthly schedule.
What does Study Protocol Planner deliver?
Every run delivers a sourced report, with every claim linked to its source.
Can I change what Study Protocol Planner does?
Yes. Every GREP AI agent can be cloned into your workspace, where you can edit its instructions, add your own sources and files, and change its schedule.
Which reporting guideline does the research protocol follow?
The one that matches the study type, such as CONSORT for randomized trials and A/B tests, SPIRIT for trial protocols, STROBE for observational studies, COREQ for interviews and CHERRIES for web surveys. Others are found through the EQUATOR Network.
How is the sample size calculated?
With code execution, such as statsmodels or scipy, using the test that matches the primary endpoint. If the required n doesn't fit your constraints, it reports the minimum detectable effect the feasible n can detect, or the duration needed to reach the required n. For qualitative work, it justifies n with saturation or information-power literature instead.
Is the protocol medical or legal advice?
No. The design, sample size and regulatory status are recommendations for you to confirm. For a clinical or health intervention, it states that a qualified investigator and the ethics committee must approve the protocol before enrollment.
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Run Study Protocol Planner in minutes.
Free to start. Run it once, put it on a schedule, or clone it and make it yours.