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Clinical Trials in Canada / NCT07693803
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The Creative Team Member: A Study of the Influence of AI Integration Timing on Brainstorming and Ideation

NCT07693803 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2026-07-20
Last updated
2026-07-14

Condition(s) studied

Creativity

Investigational drug(s) / intervention(s)

Artificial Intelligence First (Early Integration)Artificial Intelligence Last (Late Integration)

Artificial Intelligence First (Early Integration): The introduction of ChatGPT Pro (GPT-4o architecture) at the beginning (minute 0) of a 12-minute group brainstorming session. A single prompt containing the scenario is submitted to generate an initial set of ideas, with no further back-and-forth dialogue permitted. This single artificial intelligence output serves as the baseline for the team's subsequent human ideation.

Artificial Intelligence Last (Late Integration): The introduction of ChatGPT Pro (GPT-4o architecture) at the midpoint (minute 6) of a 12-minute group brainstorming session. A single prompt containing both the scenario and the team's already-generated human ideas is submitted, with no further back-and-forth dialogue permitted. This single artificial intelligence output is used to guide the team's human ideation for the remaining 6 minutes.

Study summary

This study aims to examine how the timing of artificial intelligence (AI) integration during group brainstorming activities affects the creativity and ideation of participants. Undergraduate student participants will be randomly allocated into teams of four to complete a structured 12-minute brainstorming task. The study utilizes a three-group experimental design to compare three conditions: no AI access, AI access from the outset of the session, and AI access introduced halfway through the session. The standardized generative AI tool used is ChatGPT Pro. The creative output produced by each group will be evaluated by a panel of independent expert judges using the Consensual Assessment Technique (CAT).

Eligibility

Sex
ALL
Min age
—
Max age
—
Healthy volunteers
Accepted
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

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
McMaster University Hamilton Ontario

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07693803 on ClinicalTrials.gov ↗ ← All trials in Canada