When to bring AI into a brainstorm: early or late? small study tests the timing effect on creativity
NCT ID NCT07693803
First seen Jul 09, 2026 · Last updated Jul 15, 2026 · Updated 3 times
Summary
This study investigates whether the timing of introducing an AI tool (ChatGPT Pro) during a group brainstorming session affects the creativity of the ideas generated. Undergraduate students work in teams of four on a 12-minute brainstorming task, with some groups using AI from the start, some halfway through, and some not at all. Independent judges rate the creativity of the ideas. The goal is to understand the best way to integrate AI into collaborative creative work.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ChatGPT Pro (GPT-4o architecture)
- What this could lead to
- If it works, this could point toward the best way to use AI tools to boost creative teamwork in education and business.
- What could go wrong
- This is a very small, early-stage study with only 16 participants, so results may not apply broadly. The task is artificial and may not reflect real-world creativity.
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.
- Participants
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About 16 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Sep 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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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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.
Inclusion Criteria: * Enrolled as a student in the designated summer research program * Able to provide voluntary informed consent * Proficient in reading and communicating in English (required to engage with the scenarios and the artificial intelligence tool) Exclusion Criteria: -Not enrolled as an undergraduate student
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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McMaster University
Hamilton, Ontario, L8S 4L8, Canada
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