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临床试验/NCT00032539
NCT00032539已完成不适用

CSP #476CC - Enhancing Quality of Informed Consent (EQUIC-CC) Customized Consent

US Department of Veterans Affairs4 个研究点 分布在 1 个国家目标入组 240 人开始时间: 1999年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
240
试验地点
4
主要终点
improve method of disclosing information to patients in the informed consent process

研究概览

简要总结

Patients in 'parent' cooperative study projects are interviewed about their experiences in the informed consent process.

详细描述

Intervention: (1) Cognitive stratification (obtained by a test of cognitive ability, followed by a tailored IC process); (2) Pre-recruitment video (a patient-activation video designed to prevent several common misconceptions; (3) Provide prospective research volunteers with a sense of the purpose and methods of controlled research); and (4) Evaluation of the informed consent process using the Brief Informed Consent Evaluation Protocol (BICEP) developed in EQUIC-DP.

Primary Hypothesis: The validity of informed consent can be improved, as measured by an independent interview of patients (BICEP), by at least one of three interventions described above.

Primary Outcomes: The quality of the informed consent process, as measured by the BICEP (Brief Informed Consent Evaluation Protocol). The BICEP also offers a method to certify informed consent in routine use.

Study Abstract: Customized Consent will develop and test an innovative, supplemental method of disclosing information to patients in the informed consent process. This disclosure strategy is intended to increase patients' understanding and satisfaction with the consent process. This study has two goals:

  • to evaluate the effectiveness of an intervention to improve comprehension during informed consent; and
  • to identify those patients for whom this intervention is most effective.

研究设计

研究类型
Observational
观察模型
Case Crossover
时间视角
Retrospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Inclusion Criteria:
  • Depends on 'parent' study

排除标准

  • Exclusion Criteria:
  • Depends on 'parent' study

结局指标

主要结局

improve method of disclosing information to patients in the informed consent process

时间窗: post-randomization

次要结局

未报告次要终点

研究者

申办方类型
Fed
责任方
Sponsor

研究点 (4)

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