Actively Recruiting

Phase Not Applicable
Age: 18Years - 45Years
All Genders
Healthy Volunteers
NCT06386588

The Effects of Auditory Stimulation During Sleep on Brain Networks in Schizophrenia

Led by Massachusetts General Hospital · Updated on 2025-05-14

60

Participants Needed

1

Research Sites

151 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

In this research study the investigators will use sleep headbands to measure brain rhythms and to improve their coordination across brain regions. The headbands will be worn at home for multiple nights. On some nights the headbands will play soft sounds at specific times during sleep. The investigators are interested in learning whether this timed auditory stimulation may be a strategy to improve the coordination of sleep rhythms across brain regions, improve network communication, and as a result, improve memory. The investigators will study 30 adults aged 18-45 with schizophrenia and 30 demographically matched healthy controls. Participants will first have a daytime MRI scan, during which they will complete a finger tapping motor sequence task (MST), followed by a week of sleep at home with a sleep headband. They will also do the MST at home on two of the nights. On the final day of the study, participants will return for a second MRI scan.

CONDITIONS

Official Title

The Effects of Auditory Stimulation During Sleep on Brain Networks in Schizophrenia

Who Can Participate

Age: 18Years - 45Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • 18 to 45 years old
  • Fluent in English
  • Able to give informed consent
  • For adults with schizophrenia: confirmed DSM-V diagnosis of schizophrenia
  • For adults with schizophrenia: unmedicated or on a stable dose of antipsychotic drugs
Not Eligible

You will not qualify if you...

  • Ferrous metal in the body
  • Currently pregnant or breastfeeding
  • Motor problems preventing finger tapping task
  • IQ less than 85
  • Other neurological disorders including seizure disorders
  • Significant hearing or vision loss
  • Chronic medical conditions affecting sleep
  • Unstable chronic medical conditions such as asthma, diabetes, cystic fibrosis, or cardiac disease
  • Diagnosed sleep disorder other than insomnia
  • History of head injury with prolonged unconsciousness or neurological effects
  • For healthy adults: history of mental illness
  • For healthy adults: current use of psychotropic medications or medications affecting sleep or cognition

AI-Screening

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Trial Site Locations

Total: 1 location

1

Massachusetts General Hospital

Charlestown, Massachusetts, United States, 02129

Actively Recruiting

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Research Team

L

Lindsey Jones, MS

CONTACT

D

Dara Manoach, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

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