Full research protocol generation / 完整研究方案 / 方案设计工具
design_protocol_generateFull research protocol generation / 完整研究方案 / 方案设计工具 | USE WHEN: the user wants a complete research protocol including sample size, statistical plan and ethics points | ALIASES: 研究方案, 方案正文, 写方案, 方案生成, protocol, full protocol | RETURNS: 完整研究方案 JSON(14 段)或单项工具结构化结果;缺参时返回 needs_user_input 明确列出缺什么,不返回编造值
Tool call template
Replace each placeholder with a value matching the input schema. Only required parameters are included; add optional parameters as needed.
{
"id": 1,
"jsonrpc": "2.0",
"method": "tools/call",
"params": {
"arguments": {
"tool_name": "<tool_name>"
},
"name": "design_protocol_generate"
}
}Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| p1 | No | 二分类结局:试验组预期发生率(0~1) | |
| p2 | No | 二分类结局:对照组预期发生率(0~1) | |
| alpha | No | 显著性水平,默认 0.05 | |
| power | No | 检验效能,默认 0.80 | |
| topic | No | 研究选题(一句话) | |
| design | No | 指定设计类型(rct/cohort/case_control/cross_sectional);不填则由 PICO 自动推荐 | |
| outcome | No | O:主要终点指标(如“28天病死率”“总生存期”“HbA1c 变化值”) | |
| n_groups | No | 分组数,默认 2 | |
| n_centers | No | 参与中心数,默认 1 | |
| tool_name | Yes | 工具名。推荐 full_proposal(一次输出完整方案)。可选:full_proposal / eligibility_criteria / intervention_detail / randomization / blinding_plan / bias_control / budget_gantt / sample_size_calc / spirit_check / compliance_check | |
| comparison | No | C:对照措施(安慰剂/标准治疗/未暴露) | |
| event_rate | No | 生存结局:观察期内事件发生率(0~1) | |
| n_subjects | No | 受试者例数(预算估算用;不填则用样本量计算结果) | |
| population | No | P:目标人群(疾病/年龄/严重程度) | |
| effect_size | No | 连续结局的标准化效应量 Cohen's d | |
| dropout_rate | No | 预计脱落率,默认 0.10 | |
| hazard_ratio | No | 生存结局:预期风险比 HR(≠1) | |
| intervention | No | I:干预或暴露措施 | |
| outcome_type | No | 主要终点数据类型:continuous / binary / time_to_event / count;不填按指标名自动识别 | |
| completed_steps | No | spirit_check / compliance_check 用:已完成的方案步骤编号(1~9) | |
| duration_months | No | 研究周期(月),默认 24 | |
| primary_timepoint | No | 主要终点评价时点(如“治疗 12 周”) | |
| secondary_outcomes | No | 次要终点,多个用分号分隔 |