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Study identifier: NCT06378450 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Dose-Response Effects of Mindfulness Meditation

Condition: Well-Being, Psychological · Depression  ·  Sponsor: University of Melbourne

PhaseNA
Planned participants860
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersYes

About this study

The goal of this randomized controlled trial is to test for evidence of dose-response effects in a sample of healthy adults with little to no prior experience with meditation. The main question it aims to answer is whether larger doses of mindfulness meditation yield greater positive changes in wellbeing than smaller doses. Our hypotheses are that (1) larger doses of mindfulness training will yield significantly larger effects, and (2) different doses will be significantly associated with variation in participant engagement, with lower engagement associated with higher doses. Researchers will compare each of three dose conditions, 10-min, 20-min, 30-min, against a minimal dose condition of 3-4 min. Participants will take a 28-day mindfulness meditation course, with guided audio instructions provided daily throughout the intervention period (excluding one rest day per week). They will also be asked to respond to surveys before, during, and after the intervention.

This description comes directly from the study's public registry record.

Talk to the study team

Nicholas T Van Dam, PhD  ·  +61 3 8344 3644  ·  nicholas.vandam@unimelb.edu.au

Nicholas I Bowles  ·  +61 3 8344 3644  ·  nbowles@student.unimelb.edu.au

Always discuss trial participation with your own doctor first.

Locations (1)

Contemplative Studies Centre, The University of MelbourneCarlton, Victoria, AustraliaRecruiting

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Source record: clinicaltrials.gov/study/NCT06378450