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NCT Number: NCT05565833

Sleep Healthy Using the Internet Mitigating Insomnia to Address Neurocognitive Difficulties (SHUTi MIND)

This randomized controlled trial will evaluate the impact of an Internet-delivered cognitive behavioral therapy for insomnia (CBT-I) intervention on sleep and the extent to which it contributes to cognitive health in individuals with mild cognitive impairment. Participants with insomnia who meet the study criteria for mild cognitive impairment will be recruited to determine the effects of the CBT-I intervention compared to a patient education condition on sleep and cognition. Internet-based recruitment methods will be used, and outcomes include sleep variables, daytime variables, and cognitive status.

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Key information

About this study

This randomized controlled trial will evaluate the impact of an Internet-delivered cognitive behavioral therapy for insomnia (CBT-I) intervention on sleep and the extent to which it contributes to cognitive health in individuals with mild cognitive impairment. Participants with insomnia who meet the study criteria for mild cognitive impairment will be recruited to determine the effects of the CBT-I intervention compared to patient education (PE) control condition on sleep and cognition. Internet-based recruitment methods will be used, and outcomes include sleep variables (reduced overall insomnia severity and wake after sleep onset), daytime variables (reduced levels of fatigue, improved quality of life, and improved mood), and cognitive status (memory, attention/psychomotor speed, and executive functioning domains). Participants will complete a pre-assessment battery, which consists of an online cognitive test, an online questionnaire, and two weeks of sleep diaries. Once complete, participants will be randomized to either the Internet-based PE or CBT-I intervention. At the start of week nine, all participants will be instructed to complete the post-assessment battery (cognitive test, questionnaires, and diaries). After completing the post-assessment, participants will have continued access to their assigned online program throughout the study duration. This same assessment (cognitive test, questionnaires, and diaries) will be completed at 6, 12, 18, and 24 months.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Provision of signed and dated informed consent form
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • Male or female, aged ≥ 65 years of age.
  • Able to speak and read English, and is a US resident.
  • Have access to any Internet-enabled device (computer, tablet, smartphone) and willing to be emailed about the study.
  • Sleep-onset insomnia and/or sleep maintenance insomnia symptoms
  • The sleep disturbance (or associated daytime fatigue) causes significant distress or impairment in social, occupational, or other areas of functioning over the past three months.
  • Cognitive impairment through study assessment.
  • Stable medication regimen unless medication is known to cause insomnia

Exclusion criteria

  • Current psychological treatment for insomnia
  • Initiation of psychological or psychiatric treatment within the past three months
  • 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
  • Not recovered from a brain tumor, injury, or infection
  • Epilepsy without stable treatment for at least 3 months
  • Irregular sleep schedule
  • Use of stimulating medications after 5pm or taken for less than 3 months
  • Psychotic or bipolar disorder
  • Moderate to high risk of suicide
  • Alcohol or drug abuse within the past year
  • Other untreated sleep disorders (e.g., obstructive sleep apnea)
  • Study screen for severe depression

Treatment and study plan

SHUTi OASIS

Behavioral

Cognitive Behavioral Therapy for insomnia delivered online and metered out over 6-9 weeks in a fully automated, interactive, tailored web-based program

Patient Education

Other

An educational website containing information on insomnia

Primary outcomes

  1. Insomnia Severity Index

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Change in overall insomnia severity

Secondary outcomes

  1. Wake after sleep onset (WASO)

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Change in periods of wakefulness occurring after defined sleep onset as measured by daily sleep diaries over 10-14 day periods, measured in minutes, collected through sleep diary entries

  2. Sleep onset latency (SOL)

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Change in length of time that it takes to transition from wakefulness to sleep, measured in minutes, collected through sleep diary entries

  3. Multidimensional Fatigue Symptoms Inventory - Short Form

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Change in self-report measures of five dimensions of fatigue ( general fatigue, physical fatigue, emotional fatigue, mental fatigue, and vigor) measured using Multidimensional Fatigue Symptoms Inventory-Short Form. Total MFSI-SF scores range from 24 to 96, with a higher score indicating a higher fatigue level

  4. Short Form-12 Health Survey (Quality of Life)

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    The SF-12 Health Survey will be used to measure changes in physical and mental quality of life. Scores range from 0 to 100, with higher scores indicating better physical and mental health

  5. Match to Sample Visual Search

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Changes in attention and processing speed will be measured using the Cambridge Neuropsychological Test Automated Battery (CANTAB) Match to Sample Visual Search

  6. Spatial Working Memory Test

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Changes in working memory and executive function will be measured using the Cambridge Neuropsychological Test Automated Battery (CANTAB) Spatial Working Memory Test

  7. Paired Associates Learning

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Changes in episodic memory will be measured using the Cambridge Neuropsychological Test Automated Battery (CANTAB) Paired Associates Learning

  8. Sleep Efficiency

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Amount of time spent asleep divided by the total time in bed

Other outcomes

  1. Insomnia Knowledge Scale

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Sleep knowledge and cognitive behavioral therapy for insomnia techniques; scores range from 0-10 and higher scores indicate greater insomnia knowledge

  2. Center for Epidemiologic Studies Depression Scale (CES-D)

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Depression and anxiety are measured using the Center for Epidemiologic Studies Depression Scale (CES-D). Scores range from 0-60, where higher scores indicate greater likelihood of depression

  3. Falls frequency

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Falls questionnaire including number and frequency of falls

  4. Patient-Reported Outcomes Measurement Information System (PROMIS)

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Pain intensity and interference are measured using PROMIS Pain Intensity questions. On a scale of 0-100, a score of 50 is considered the mean/reference population, and higher scores indicate greater pain intensity.

  5. Self-Efficacy Scale- Insomnia-Specific

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Global-, task-, and self-regulation self-efficacy changes are measured using Self-Efficacy Scale developed by Bouchard, Bastien & Morin (2010) and includes 40 questions. Questions are answered using a scale from 0 (can't do at all) to 100 (absolutely certain can do), where higher scores indicate higher self-efficacy.

  6. Lawson's Instrumental Activities of Daily Living Scale

    Time frame: Baseline, 9 weeks, 6 months, 12 months, 18 months, and 24 months

    Activities that allow an individual to live independently in a community. Score range from 0 (low function, dependent) to 8 (high function, independent).

Study contacts

Contact information is provided by the study sponsor or research team.

Meghan K Mattos, PhD, RN, CNL

CONTACT

[email protected]

434-243-3936

Sponsors and collaborators

Lead sponsor

University of Virginia

Other

Registry information

Official study title

Internet-based Insomnia Intervention to Prevent Cognitive Decline in Older Adults With Mild Cognitive Impairment (SHUTi MIND)

Important dates

Study start
2023
Primary completion
2028
Study completion
2028
First posted
Oct 4, 2022
Registry last updated
May 8, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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