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Not yet recruiting NCT07014982

Remote Assessment of Digital Neurologic Testing

No phase Interventional Neurology

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: Guided Meditation.
Who it may be relevant to
Registry conditions: Neurology. 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

Remote Assessment of Digital Neurologic Testing (RADiaNT)

Overview

The RADiaNT study investigates whether guided meditation, using the Muse™ headband and biofeedback app, can improve sleep, mood, and cognitive performance, aiming to assess its impact on mental and emotional well-being.

Interventions

  • Behavioral Guided Meditation
    Participants who complete guided meditation will be asked to meditate for 5 minutes a day, five times a week for two 6-week periods.

Primary outcome measures

  • Duration in slow wave sleep [Time frame: 17 weeks]
  • Proportion in slow wave sleep [Time frame: 17 weeks]
  • Perceived Stress Scale [Time frame: 17 weeks]
Secondary outcome measures (4)
  • Patient Health Questionnaire 9-item (PHQ-9) [Time frame: 17 weeks]
  • General Anxiety Disorder 7-item (GAD-7) [Time frame: 17 weeks]
  • Cognitive Performance [Time frame: 17 weeks]
  • Cognitive Performance [Time frame: 17 weeks]

Eligibility criteria

Inclusion criteria

  • Cognition unimpaired or mild cognitive impairment
  • Fluent in English
  • United States resident
  • Able to tolerate wearing Muse headband
  • basic competence in using electronic devices (Smartphone or tablet) to engage with the Muse application and complete digital surveys and assessments

Exclusion criteria

  • Neurological and Brain Disorders
  • Not Fluent in English
  • Not a US Resident
  • Unable to tolerate wearing Muse Headband

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
Treatment

Study locations

United States · 1 center
  • Mayo Clinic — Rochester

Identifiers

NCT: NCT07014982 · 24-013687

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗