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New study aims to keep AI in research honest and ethical

NCT ID NCT07340905

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study is developing a tool to help researchers use artificial intelligence (AI) ethically in their work. AI is now used in many steps of research, from analyzing data to writing papers, but it can raise ethical concerns like bias or privacy. The study will ask 200 people who have experience with research or AI to test the tool and give feedback.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could provide a standardized way to evaluate the ethical use of AI in research, helping researchers avoid bias and privacy issues.
What could go wrong
This is an early-stage observational study with no intervention, so it will not directly treat any disease. The tool may not be widely adopted or may need further refinement.

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.

Participants

About 200 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Jan 2027

An estimate. End dates often move.

Lead sponsor

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.

Who is studied

Principal investigators / co-investigators Research assistants / lab members Data scientists / statisticians Students (Masters/PhD) working on AI-supported research

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show 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 * Age ≥ 18 * Able to provide informed consent * Has direct experience with research and/or AI tools used in research (often within the last 1-3 years) * Speaks/reads the study language (e.g., English/Arabic) * Available to complete the study activity (survey) * Exclusion criteria * No AI is involved. * It's only theory/principles with no checklist or questions. * It covers only one issue (privacy-only, bias-only) when you need full ethics. * Not enough info to assess (no data source, no model description, no intended use). * It's a small classroom/toy example with no real impact.

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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.

  1. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  2. 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.

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