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Clinical Trials/NCT03256760
NCT03256760
Completed
Phase 1

Experimental Model of Depression in Aging: Insomnia, Inflammation, and Affect Mechanisms

Michael Irwin, MD1 site in 1 country160 target enrollmentJanuary 1, 2018

Overview

Phase
Phase 1
Intervention
Endotoxin
Conditions
Depression in Old Age
Sponsor
Michael Irwin, MD
Enrollment
160
Locations
1
Primary Endpoint
Depressed Mood Subscale of the Profile of Mood States (POMS)
Status
Completed
Last Updated
last year

Overview

Brief Summary

Late-life depression is a significant public health concern, and effective interventions for prevention and treatment are needed. Insomnia and inflammation are modifiable targets for depression prevention, and this study is significant in using an experimental approach (i.e., inflammatory challenge) to probe acute inflammatory- and depression responses as a function of insomnia, which will inform identification of molecular targets for pharmacologic interventions, and improvement of insomnia treatments to prevent depression in older adults.

Project

Detailed Description

This study (SHARE-D) will use an inflammatory challenge (i.e., endotoxin) to probe acute inflammatory- and depression responses (primary outcome) in older adults as a function of insomnia. Older adults with insomnia show chronic inflammation; sleep disturbance also activates inflammatory signaling; chronic inflammation primes acute inflammatory responses; chronic inflammation, as well as acute inflammatory reactivity, predict depression over the following year; and finally, endotoxin induces acute inflammation along with depressive symptoms, with preliminary evidence that "two-hits" (i.e., sleep disturbance and inflammatory challenge) are associated with exaggerated increases in depression, especially in women. In this placebo-controlled, randomized, double-blind study of low dose endotoxin in older adults (60-80 y; stratified by sex) with insomnia (n=60) vs. comparisons without insomnia (n=100), the investigators hypothesize that older adults with insomnia will show heightened inflammatory- and affective responding to inflammatory challenge as compared to those without insomnia. The investigation aims to: 1) examine differences in depressive symptoms and measures of negative affect responding as a function of insomnia and inflammatory challenge; 2) examine differences in measures of positive affect responding as a function of insomnia and inflammatory challenge; and 3) examine differences in experimentally-induced inflammation in relation to depressive symptoms and measures of negative- and positive affect responding as a function of insomnia.

Registry
clinicaltrials.gov
Start Date
January 1, 2018
End Date
April 30, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Michael Irwin, MD
Responsible Party
Sponsor Investigator
Principal Investigator

Michael Irwin, MD

Principal Investigator

University of California, Los Angeles

Eligibility Criteria

Inclusion Criteria

  • Participants will be required to be in good general health (as evaluated during the phone and in-person baseline session)
  • Participants will be aged 60 to 80 years.
  • Half the participants (N=80) will be those with insomnia disorder as diagnosed by the Structured Clinical Interview for Diagnosis, Diagnostic Statistical Manual 5 and the Duke Structured Interview for Sleep Disorders, .
  • The other half will be those without insomnia identified as not having insomnia by any of these assessments.

Exclusion Criteria

  • Following a structured telephone interview, prospective participants with the following conditions will not advance to the in-person baseline session:
  • Presence of chronic mental or physical illness (except for insomnia)
  • History of allergies, autoimmune, liver, or other severe chronic diseases,
  • Current and regular use of prescription medications such as steroids, non-steroid anti-inflammatory drugs, aspirin, immune modifying drugs, opioid analgesics, statins, antihypertensive drugs, anti-arrhythmic drugs, and antidepressant medications (none in the last 6 months); and nightshift work or time zone shifts (\> 3hrs) within the previous 6 weeks, or previous history of fainting during blood draws.
  • Presence of co-morbid medical conditions not limited to but including cardiovascular (e.g., history of acute coronary event, stroke) and neurological diseases (e.g., Parkinson's disease), as well as pain disorders;
  • Presence of comorbid inflammatory disorders such as rheumatoid arthritis or other autoimmune disorders;
  • Presence of an uncontrolled medical condition that is deemed by the investigators to interfere with the proposed study procedures, or to put the study participant at undue risk;
  • Presence of chronic infection, which may elevate proinflammatory cytokines;
  • Presence of an acute infectious illness in the two weeks prior to an experimental session.
  • Current Axis I psychiatric disorders as determined by the Research Version of the Structured Clinical Interview including a current major depressive disorder and substance dependence (a prior history of depression is not an exclusion criterion, which will be considered for a pre-planned sensitivity analysis and will be used as a pre-classification variable in the generation of the two groups, and in the randomization schedule);

Arms & Interventions

Endotoxin

Endotoxin 0.8 ng/kg body weight

Intervention: Endotoxin

Placebo

Placebo

Intervention: Placebo

Outcomes

Primary Outcomes

Depressed Mood Subscale of the Profile of Mood States (POMS)

Time Frame: 12 hours

The Depressed Mood Subscale of the POMS is a self-and observer rated assessment of depressed mood in which severity of depressed mood is rated using a visual analog scale from 1 to 5 (5 being most severe). Each timepoint is scored and analyses examine the temporal profile of change with assessment every hour

Depressed mood and depressive symptoms as measured by the Montgomery Asberg Depression Rating Scale (MADRS)

Time Frame: 8 hours

Depressed mood and depressive symptom severity by self-reported assessment using the Montgomery Asberg Depression Rating scale with a range from 0 to 54 with a higher score indicating more severe depressive symptoms. Each timepoint is scored and analyses examine the temporal profile of change with assessment every 2 hours

Secondary Outcomes

  • Emotion Intensity Task(about 2 hours)
  • Effort Expenditure for Reward Task(about 2 hours)
  • Temporal Experience of Pleasure Scale(8 hours)
  • Hamilton Depression Rating Scale(8 hours)
  • Emotion Facial Recognition Task(about 2 hours)
  • Social Reward Task(about 2 hours)
  • Probabilistic Reward Task(about 2 hours)
  • Snaith-Hamilton Pleasure Scale(8 hours)

Study Sites (1)

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