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Recruiting NCT07740148

Human-Created vs AI-generated Art on Immediate Psychological Responses

No phase Interventional Psychological Well-Being

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Human-created Animated Art Film, AI-generated Comparator Film.
Who it may be relevant to
Registry conditions: Psychological Well-Being. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Unsure about the terms? Read our patient guide →

Official title

Immediate Psychological Effects of a Brief Human-Created Animated Art Film: A Three-Arm Online Randomized Controlled Trial

Overview

This online randomized controlled trial will evaluate the immediate psychological effects of a brief human-created animated art film. U.S.-based adults recruited through Prolific will be randomized in Stanford Qualtrics to view a human-created animated art film, view an AI-created comparison video, or to a do-nothing control arm. Outcomes will be assessed immediately after exposure.

Interventions

  • Other Human-created Animated Art Film
    A brief, \~3min human-created art film featuring 2D animation, dance, song and instrumental music.
  • Other AI-generated Comparator Film
    A brief, \~3min AI-generated film featuring 2D animation, dance, song and instrumental music.

Primary outcome measures

  • State Moral Elevation [Time frame: Immediately after assigned exposure, within the single study session (approximately 10 minutes after enrollment).]
Secondary outcome measures (4)
  • Change From Baseline in State Empathic Concern [Time frame: Baseline and immediately after assigned exposure, within the single study session.]
  • Change From Baseline in State Social Connection [Time frame: Baseline and immediately after assigned exposure, within the single study session]
  • Change From Baseline in State Hope [Time frame: Baseline and immediately after assigned exposure, within the single study session.]
  • Change From Baseline in Motivation to Improve Close Relationships [Time frame: Baseline and immediately after assigned exposure, within the single study session.]

Eligibility criteria

Inclusion criteria

  • Resides in the United States
  • Able to read and understand English
  • Current Prolific participant
  • Able to provide electronic informed consent
  • Able to complete the study online using a computer or mobile device with internet access

Exclusion criteria

  • Residence outside the United States
  • Unable to read and understand English sufficiently to complete the study
  • Does not provide electronic informed consent
  • Prior participation in this study

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Prevention

Study locations

United States · 2 centers
  • Prolific Academic Online Academic Research Platform — Palo Alto
  • Stanford University — Stanford

Identifiers

NCT: NCT07740148 · 86234

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗