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Not yet recruiting NCT07607782

Effect of a Brief Daily Digital Meditation on Well-Being in US Young Adults (BEGIN II)

No phase Interventional Mental Health and General 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: Miracle of Mind meditation, Neutral audio learning task.
Who it may be relevant to
Registry conditions: Mental Health and General Well-being. Basic parameters: 18 years — 40 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
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This study is testing whether a short, daily, app-based meditation can help young adults feel better in their everyday lives. We will invite about 354 adults between 18 and 40 years old who live in the United States to join. Everyone who joins will be randomly placed into one of three groups for 4 weeks: Intervention group will do a 7-minute Miracle of Mind meditation each day using a phone app. Active comparator group will listen to a neutral 7-minute audio lesson each day. Control group will continue their usual daily routine without adding anything new. All participants will answer short online surveys at the start and several times during the 4 weeks, sharing how they feel about their mood, stress, anxiety, overall well-being, and mindfulness. Participants who already wear a smartwatch (like a Fitbit or Apple Watch) can choose to share their heart rate-related data so we can see whether the meditation might also affect physical signs of stress. Investigators will compare how participants in the three groups change over time to see if the daily 7-minute meditation helps young adults feel better, less stressed, and more emotionally resilient.

Interventions

  • Behavioral Miracle of Mind meditation
    Miracle of Mind is a 7-minute meditation that incorporates breath and awareness to enhance mental health and clarity. The practice involves voice-guided seated meditation with simple breathing techniques. This is a simple, safe intervention that does not require any previous meditation experience.
  • Behavioral Neutral audio learning task
    Active control participants are asked to listen to an approximately 7-minute neutral audio learning task daily in the 3Cs app for the duration of the study. A total of 28 audio learning tasks were sourced from the SDG Academy and Harvard University YouTube and SoundCloud content were screened prior to inclusion.

Primary outcome measures

  • Well-being [Time frame: "Baseline, Week 2 and Week 4"]
Secondary outcome measures (3)
  • Mindfulness [Time frame: "Baseline and 4 weeks"]
  • Overall health [Time frame: "Baseline, Week 2 and Week 4"]
  • Stress and Anxiety [Time frame: "Baseline, Week 1, Week 2, Week 3 and Week 4"]

Eligibility criteria

Inclusion criteria

  • Individuals between the ages of 18-40 years
  • Currently residing in the USA
  • Individuals who are English speaking
  • Willing and able to download an application on iOS/Android

Exclusion criteria

  • Individuals who are non-English speaking
  • Unable to access an iOS/Android smartphone
  • Individuals who regularly practice any form of meditation >4 times per week
  • Individuals scoring 9-12 on the PHQ-4, or ≥3 on either the PHQ-2 or GAD-2 subscale

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

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07607782 · 2026P000078

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗