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Treating Insomnia in Mild Cognitive Impairment

Key facts

Where
Boston, United StatesSee the site

Where in United States

  • Beth Israel Deaconess Medical CenterBoston, United StatesContact: Alex Clinical Research CoordinatorTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

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Trial details

Who runs it
Beth Israel Deaconess Medical Center
Trial code
NCT06687161
Record updated
5 November 2026
Original description
The goal of this study is to test a new way to improve sleep quality in persons living with mild cognitive impairment. The treatment combines a safe and gentle way to stimulate the brain, called transcranial magnetic stimulation, with a psychological treatment, called cognitive behavioral therapy for insomnia.Read full original descriptionShow less

Neuromodulation and Cognitive Behavioral Therapy for Insomnia in MCI

The goal of this study is to test a new way to improve sleep quality in persons living with mild cognitive impairment. The treatment combines a safe and gentle way to stimulate the brain, called transcranial magnetic stimulation, with a psychological treatment, called cognitive behavioral therapy for insomnia.

Inclusion: Aged 60 years or older; Speak and read English; Clinical diagnosis of MCI or Subjective Cognitive Impairment (SCI)-a perceived gradual worsening in cognitive ability relative to one's younger self, or peer group-reported by either the participant or informant; Reported insomnia symptoms (sleep-onset and/or sleep maintenance) that cause significant distress or impairment in social, occupational, or other areas of functioning over the past three months; Have access to an Internet-enabled computer or tablet at home, or ability to connect a BIDMC-provided tablet to the internet, with private space to complete cognitive testing; Capable of and willing to provide written informed consent.

Exclusion: Alcohol or drug abuse within the past year; Evidence of significant cognitive impairment or dementia; Uncontrolled moderate-to-severe obstructive sleep apnea or other untreated sleep disorder (e.g., Restless Leg Syndrome, Periodic Limb Movement Disorder, parasomnia). Sleep apnea that is managed (e.g., regular use of a CPAP) and stable for ≥3 months is allowed; Diagnosis of Parkinson's disease, Huntington's disease, Lewy-Body disease, or other neurological condition known to impact sleep; Current diagnosis of major psychiatric disorder (well-controlled depression or anxiety is permitted); Contraindications for TMS or MRI; Current psychological treatment for insomnia; Current opiate/opioid use; Irregular sleep schedule (bedtime before 8pm/after 2am OR wake time before 4am/after 10am), unless participant states they are willing and able to change if prompted.

ClinicalTrials.gov NCT06687161