Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
Healthy Volunteers
NCT07102953

Mindfulness on Creativity

Led by Zhejiang University · Updated on 2025-08-05

111

Participants Needed

1

Research Sites

14 weeks

Total Duration

On this page

Sponsors

Z

Zhejiang University

Lead Sponsor

W

Westlake University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Purpose of the Study This clinical trial aims to find out whether a 5-day mindfulness training program can help improve creativity in academic researchers. The study focuses on answering these key questions: Can focused-attention (FA) and open-monitoring (OM) meditation boost creativity in academic researchers? Do FA and OM meditation have different effects on creativity? How does the training affect brain activity (measured by electrical signals)? Researchers will compare the effects of FA and OM meditation with a control group that listens to audio recordings, to see which method-if any-helps improve creativity. What Participants Will Do Join one of three groups: FA meditation, OM meditation, or audio listening (control), and take part in daily practice for 5 days. Come to the research center for testing three times. Keep a daily log of how they engage with the training.

CONDITIONS

Official Title

Mindfulness on Creativity

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Currently enrolled graduate students (Master's or PhD) or other research personnel such as postdoctoral fellows, research assistants, or academic researchers.
  • Aged 18 years or older and under 65 years.
  • No current diagnosis of severe mental disorders like schizophrenia, schizoaffective disorder, or bipolar disorder.
  • Not currently taking mood-stabilizing medications such as SSRIs to avoid effects on mindfulness training and EEG results.
Not Eligible

You will not qualify if you...

  • Participating in other mindfulness-based psychological intervention programs or courses that cannot be paused during the study.
  • Suicidal thoughts or plans reported in the past two weeks.
  • Unable to attend in-person assessments at the laboratory.
  • Refusal or inability to provide informed consent.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Westlake University

Hangzhou, Zhejiang, China, 310030

Actively Recruiting

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Research Team

R

Rong Li, Assisstant researcher

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

3

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