Clinical trial · Interventional
Improving Consent Experiences in Clinical Trials
Improving Consent Experiences in Clinical Trials at Siteman Cancer Center
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Why stopped (as posted): Did not receive funding
Summary
Brief summary (as posted)
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
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Cancer | Malignant Neoplasm | ALIAS | 0.90 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Standard Consent Form | Behavioral | — | UNRESOLVED |
| Visual Key Information (VKI) page | Behavioral | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- type
- ACTIVE_COMPARATOR
- label
- Standard consent forms
- description
- The approved standard consent form will be used during the consent processes.
- interventionNames
- Behavioral: Standard Consent Form
- type
- EXPERIMENTAL
- label
- Standard consent forms with a visual key information (VKI) page
- description
- The approved standard consent form with a VKI page will be used during the consent processes.
- interventionNames
- Behavioral: Standard Consent Form
- Behavioral: Visual Key Information (VKI) page
- type
- EXPERIMENTAL
- label
- Research Team Members
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Patient Eligibility Criteria: * Patient must be 18 years or older * Patients must be English-speaking * Able to understand an IRB-approved written consent document * Must go through the consent process for one of the parent studies Research Team Eligibility Criteria: * Member of a parent study research team * Engaged in the study consent processes, including creating and reviewing consents or enrolling participants
References
Publications (0)
Data not yet available