Cancer consent study pulled before it began
NCT ID NCT07293520
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study was designed to test whether adding a simple visual summary page to standard consent forms helps cancer patients better understand what they are signing up for and feel less anxious. It planned to enroll adults with cancer who were already joining other clinical trials. However, the study was withdrawn before any participants were enrolled, so no results are available.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Started
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Nov 2025
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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Other studies related to the condition(s) this trial covers.
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