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Completed

NCT Number: NCT07102953

Mindfulness on Creativity

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.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Westlake University

Hangzhou, Zhejiang, 310030, China

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

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

Exclusion criteria

  • Simultaneously participating in other mindfulness-based psychological intervention programs or courses that cannot be paused during the study period.
  • Suicidal ideation or planning reported within the past two weeks.
  • Inability to attend in-person assessments at the laboratory site.
  • Refusal or inability to provide informed consent.

Treatment and study plan

Focused-attention meditation

Behavioral

This is a type of mindfulenss meditation, which instructes participants to keep focusing on own breathing with a sitting and rest posture.

Open-monitoring meditation

Behavioral

This is a type of mindfulenss meditation, which instructs participants to stay aware of their vision with a sitting and rest posture.

Audio-listening control

Behavioral

Participants listen to stories about creativity with a sitting and rest posture.

Primary outcomes

  1. Divergent thinking

    Time frame: Pre- and post- assessments after a 15-min training at Day1 (before 5-day practice), Day7 (after 5-day practice), and follow-up (1 month after 5-day practice).

    Divergent thinking, a key component of creativity, will be assessed using the Alternative Uses Task (AUT). In this test, participants are asked to think of as many different uses as possible for a common object-like a brick, knife, or pillow-within a limited time. The scores including three factors: fluency, flexibility, and originality, which will be gained via TranDis, a semantic distance scoring system based on transformer-based language models.

  2. Convergent thinking

    Time frame: Pre- and post- assessments after a 15-min training at Day1 (before 5-day practice), Day7 (after 5-day practice), and follow-up (1 month after 5-day practice).

    Convergent thinking, a key component of creativity, will be measured by the Remote Associate Test (RAT). In this test, participants are given three words and must identify a fourth word that links all three.

  3. EEG

    Time frame: During the whole tests at Day7 (after 5-day practice)

    Quantitative EEG power spectral density (PSD) across frequency bands (delta: 0.5-4 Hz, theta: 4-8 Hz, alpha: 8-13 Hz, beta: 13-30 Hz, gamma: >30 Hz) will be measured at Day 7 (post-intervention). Absolute and relative power in each band will be extracted from resting-state EEG (eyes closed), task-state EEG (15-min mindfulness or control), and task-state EEG during creativity tests, recorded at standardized scalp locations. Changes in spectral power will be used as indicators of neurophysiological responses to the mindfulness training.

Secondary outcomes

  1. Mindfulness

    Time frame: Assessments at Day1 (before 5-day practice), Day7 (after 5-day practice), and follow-up (1 month after 5-day practice).

    Mindfulness is assessed using the Philadelphia Mindfulness Scale (PHLMS). The PHLMS is a 20-item scale with two factors named Awareness and Acceptance. Participants will rate on a 5-point scale (1 = never, 5 = very often) according to the frequency that they experienced the described item within the past week. The score range for the PHLMS is 20 to 100.

  2. Metacognition

    Time frame: At Day1 (before 5-day practice), Day7 (after 5-day practice), and follow-up (1 month after 5-day practice).

    Cognitive Self-Consciousness (CSC), a subscale of the Metacognition Questionnaire (MCQ), will be used to assess participants' tendency to monitor and reflect upon their own thinking processes. The subscale includes 6 items. Participants rate statements such as "I am constantly aware of the way my mind works" on a 4-point scale (1 = do not agree, 5 = agree very much). The score range is 6 to 30.

  3. Attention

    Time frame: Assessments at Day1 (before 5-day practice), Day7 (after 5-day practice).

    Sustained attention will be measured using the Sustained Attention to Response Task (SART). The SART is a computerized test for the measurement of sustained attention and response inhibition. Participants' performance will be evaluated by the time of response and the correct rate.

  4. Depression

    Time frame: Assessments at Day1 (before 5-day practice), Day7 (after 5-day practice), and follow-up (1 month after 5-day practice).

    Depression will be assessed using the Patient Health Questionnaire-9 (PHQ-9). The PHQ-9 is a 4-point scale (0 = Not at all, 3 = Nearly every day) with 9 items. The score range is 0 to 27.

  5. Anxiety

    Time frame: Pre- and post- assessments after a 15-min training at Day1 (before 5-day practice), Day7 (after 5-day practice), and follow-up (1 month after 5-day practice).

    Anxiety will be measured using the Generalized Anxiety Disorder 7-item scle (GAD-7). It is a 4-point scale (0 = Not at all, 3 = Nearly every day) with 7 items. The score range is 0 to 21.

Other outcomes

  1. Engagement and practice times

    Time frame: Day 2 to Day 5 during the intervention, and 1 month after the 5-day practice period, for participants who engaged in follow-up practice.

    Particpants will report their engagement after everyday practice by answering the question "On a scale from 0 to 10, how would you rate your level of engagement during today's practice? (0 = not engaged at all, frequent mind-wandering or drowsiness; 10 = highly engaged, focused and alert)"

Sponsors and collaborators

Lead sponsor

Zhejiang University

Other

Collaborators

  • University of Chinese Academy of Sciences
  • Westlake University

Registry information

Official study title

The Effect of Focused Attention and Open Monitoring Meditation on Creativity in Scientific Researchers

Important dates

Study start
2025
Primary completion
2025
Study completion
2025
First posted
Aug 5, 2025
Registry last updated
Jul 1, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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