Status:

COMPLETED

Use of an Internet-Based Insomnia Intervention to Prevent Cognitive Decline in Adults With Mild Cognitive Impairment

Lead Sponsor:

University of Virginia

Conditions:

Mild Cognitive Impairment

Cognitive Impairment

Eligibility:

All Genders

55+ years

Phase:

NA

Brief Summary

The purpose of the study is to determine feasibility of an online program providing cognitive behavioral therapy for insomnia in adults with cognitive impairment. The study involves the use an Intern...

Detailed Description

Mild cognitive impairment in older adults. Mild Cognitive Impairment (MCI) is recognized as an early stage cognitive disorder, a condition where patients live independently and are able to still perfo...

Eligibility Criteria

Inclusion

  • 55 years of age or older
  • ability to read and speak English
  • US resident
  • MCI diagnosis or scores within acceptable range on R-BANS assessment.
  • regular access to Internet and Email
  • willingness to use Internet and Email
  • ability to use a computer
  • no more than 6.5 hours of sleep per night
  • the sleep disturbance (or associated daytime fatigue) must cause significant distress or impairment in social, occupational, or other areas of functioning over past 3 months
  • sleep onset latency \> 30 minutes at least 3x/week for past three months; OR wake after sleep onset \>30 minutes at least 3x/week for past three months
  • Participants on stable (defined as no change in the past 3 months) medication regimens will be eligible including sleep medications, unless the medication is known to cause insomnia (e.g., steroids).

Exclusion

  • bedtime outside of 8pm-2am and arise times outside of 4-10am
  • current psychological treatment for insomnia
  • initiation of psychological or psychiatric treatment within past 3 months
  • current severe/very severe depression from QIDS-C16
  • current moderate/high risk suicide or substance use disorder in 12 months from MINI
  • other untreated sleep disorders (e.g., obstructive sleep apnea, restless legs syndrome)
  • current diagnosis of Huntington's or Parkinson's disease
  • current treatment for hyperthyroidism
  • currently undergoing chemotherapy
  • presence of asthma or respiratory concerns with night treatment
  • chronic pain treated with opioids
  • epilepsy
  • inability to provide informed consent
  • Not concurrently enrolled in any other intervention or educational study targeting sleep.

Key Trial Info

Start Date :

December 5 2018

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 28 2020

Estimated Enrollment :

12 Patients enrolled

Trial Details

Trial ID

NCT04382365

Start Date

December 5 2018

End Date

May 28 2020

Last Update

April 27 2021

Active Locations (1)

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1

University Of Virginia

Charlottesville, Virginia, United States, 22908