Pm-claude-skills research-protocol

Write a structured research protocol or study design document. Use when asked to write a research protocol, study protocol, research plan, methodology section, or research proposal. Produces a complete protocol with objectives, methodology, ethical considerations, and analysis plan.

install
source · Clone the upstream repo
git clone https://github.com/mohitagw15856/pm-claude-skills
Claude Code · Install into ~/.claude/skills/
T=$(mktemp -d) && git clone --depth=1 https://github.com/mohitagw15856/pm-claude-skills "$T" && mkdir -p ~/.claude/skills && cp -r "$T/skills/research-protocol" ~/.claude/skills/mohitagw15856-pm-claude-skills-research-protocol-d92e4b && rm -rf "$T"
manifest: skills/research-protocol/SKILL.md
source content

Research Protocol Skill

Produces structured research protocols for academic, clinical, social science, or market research studies.

Required Inputs

  • Research type (clinical trial / observational / qualitative / systematic review / survey)
  • Research question or hypothesis
  • Setting and population
  • Proposed methodology
  • Timeline
  • Funder or institution (if applicable)

Output Structure


Research Protocol: [Study Title]

Version: 1.0 | Date: [Date] | PI: [Name, institution]


1. Background and Rationale

  • What is already known
  • What the gap in knowledge is
  • Why this study is needed now

2. Research Objectives

Primary: [One clear answerable question or hypothesis] Secondary: [Additional questions]

3. Study Design

  • Design: [RCT / cohort / qualitative / mixed methods]
  • Setting: [Where]
  • Duration: [Total period and recruitment window]
  • Rationale: [Why this design fits the question]

4. Participants

Inclusion criteria: [List] Exclusion criteria: [List] Sample size: [n] — Basis: [Power calculation or saturation rationale] Recruitment: [Method and source]

5. Methodology / Intervention

For interventional: intervention description, control, randomisation, blinding For observational/qualitative: data collection methods, tools, data collectors

6. Outcomes / Measures

Primary outcome: [Measure], assessed by [method], at [timepoint] Secondary outcomes: [Measure], [method], [timepoint]

7. Data Management

  • Storage: [Where and anonymisation method]
  • Access controls: [Who can access]
  • Retention: [How long]

8. Analysis Plan

Quantitative: [Statistical test], [missing data handling], [software] Qualitative: [Framework — e.g. Braun & Clarke], [quality assurance]

9. Ethical Considerations

  • Ethics approval: [Body / reference]
  • Informed consent: [Process]
  • Confidentiality: [How maintained]
  • Risk to participants: [Assessment and mitigation]

10. Dissemination Plan

  • Target journals: [2-3 relevant]
  • Conference presentations
  • Public/patient summary

11. Timeline

PhaseActivitiesStartEnd
SetupEthics, approvals, tool development
Recruitment
Data collection
Analysis
Write-up

Quality Checks

  • Primary objective is singular and answerable (not compound)
  • Sample size has a stated basis (power calculation or saturation rationale)
  • Ethical considerations section is complete
  • Analysis plan is pre-specified (not "to be determined")
  • Timeline includes all phases from ethics approval to write-up

Example Trigger Phrases

  • "Write a research protocol for [study]"
  • "Help me design a study to investigate [question]"
  • "Write the methodology for my research proposal"