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Clinical Trials/NCT03538574
NCT03538574
Completed
Not Applicable

Mindfulness Meditation and Insomnia in Alzheimer Disease Caregivers: Inflammatory and Biological Aging Mechanisms

University of California, Los Angeles1 site in 1 country139 target enrollmentJuly 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Insomnia Chronic
Sponsor
University of California, Los Angeles
Enrollment
139
Locations
1
Primary Endpoint
Insomnia clinical response
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Treatment of insomnia in caregivers is needed given that 60% of Alzheimer disease caregivers report sleep complaints, and insomnia may add to the burden of AD caregiving and contribute to morbidity and mortality risk. This is the first intervention trial in AD caregivers to target insomnia and also evaluate two mechanisms of chronic disease risk, inflammation and cellular aging

Detailed Description

This randomized controlled trial aims to evaluate the non-inferiority of Mindful Awareness Practices for Insomnia (MAP-I ) vs. Cognitive Behavioral Therapy for Insomnia (CBT-I) on outcomes of insomnia, cellular and genomic markers of inflammation, and cellular aging in older adult AD spousal caregivers with insomnia (N=150) over one-year follow-up. The specific aims of this project are: Primary Aim 1: Determine the effects of MAP-I vs. CBT-I on subjective and objective dimensions of insomnia. Secondary Aim 1: Evaluate the effects of MAP-I vs. CBT-I on cellular and genomic markers of inflammation. Secondary Aim 2: Evaluate the effects of MAP-I vs. CBT-I on markers of cellular aging. Exploratory Aim 1: Explore moderating effects of caregiver stress (Stress and Adversity Inventory, STRAIN, number \& experienced intensity of stress exposure) on insomnia outcomes, and effects of MAP-I vs. CBT-I on caregiver stress, health functioning, chronic medical morbidity and related medication use at follow-up.

Registry
clinicaltrials.gov
Start Date
July 1, 2018
End Date
September 30, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Michael Irwin, MD

Principal Investigator

University of California, Los Angeles

Eligibility Criteria

Inclusion Criteria

  • Alzheimer or other dementia caregivers
  • Older than 45 years of age
  • Self-identified as the principal person taking care of the patient with Alzheimer or other dementia
  • Diagnostic and Statistical Manual Criteria - 5 for Insomnia

Exclusion Criteria

  • Psychiatric disorders including current major depressive disorder or other current DSM-5 psychiatric disorder (e.g. substance dependence) with the exception of anxiety disorder;
  • Psychotic symptoms;
  • Acute suicidal or violent behavior or history of suicide attempt within the last year
  • Other sleep disorders including current or lifetime history of sleep apnea, nocturnal myoclonus, phase-shift disorder as identified by SCID-5 and Duke Structured Interview for Sleep Disorders (DSISD)
  • Medical conditions such as acute or uncontrolled medical illness (e.g., major surgery, metastatic cancer, Class III heart failure, inflammatory disorder)
  • Chronic infections
  • Obesity with body mass index (BMI) \>35
  • Use of hormone containing medications including steroids or immune modifying drugs
  • Daily use of analgesics such as opioids;
  • Daily us of sedative hypnotic medications

Outcomes

Primary Outcomes

Insomnia clinical response

Time Frame: One-year

Change in severity of insomnia as measured by the Insomnia Severity Index

Secondary Outcomes

  • Insomnia clinical response(One year)
  • Daytime dysfunction(One year)
  • Inflammation(One year)
  • Cellular aging(One year)

Study Sites (1)

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