NCT07293520

Improving Consent Experiences in Clinical Trials

Improving Consent Experiences in Clinical Trials at Siteman Cancer Center

• Status: Withdrawn
• Phase: N/A
• Study type: Interventional
• Enrollment: 0 (actual)
• Sponsor: Washington University School of Medicine · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Accepted

Summary

This is a study to evaluate the impact of evidence-based visual key information (VKI) pages on participant's experiences with informed consent for research, enrollment in high-accruing studies that choose to use VKIs as part of their consent process, and research team perceptions of the implementation potential of VKIs in studies. Unlike in previous pilots conducted at Siteman Cancer Center, this study will assess changes in outcomes before and after a VKI is implemented in a study consent process.

Conditions

• Cancer

Interventions

Type	Name	Description
BEHAVIORAL	Standard Consent Form	The IRB-approved consent form will be used by research team staff during consenting process of participants for parent studies.
BEHAVIORAL	Visual Key Information (VKI) page	A VKI page will be designed for each parent study based on study materials and current consent document. The VKI will be implemented in the consent material for the study.

Timeline

• Start date: 2025-11-25
• Primary completion: 2026-12-31
• Completion: 2026-12-31
• First posted: 2025-12-19
• Last updated: 2025-12-26