Overview

Targeting Cognition in Early Alzheimer's Disease by Improving Sleep With Trazodone

Status:
Not yet recruiting

Trial end date:
2028-05-01

Target enrollment:
0

Participant gender:
All

Summary

To investigate the effect of trazodone on sleep, hippocampal-dependent memory and hippocampal excitability. The investigators hypothesize that trazodone will improve total sleep time and proportion of time in Slow Wave Sleep (SWS).

Phase:

Phase 2

Accepts Healthy Volunteers?

Details

Lead Sponsor:

Johns Hopkins University

Collaborator:

National Institute on Aging (NIA)

Treatments:

Trazodone

Criteria

Inclusion Criteria:

1. Mild Cognitive Impairment (MCI) as defined by Albert et al.2 including subjective
memory complaint and/or objective evidence of memory problems;

2. Clinical Dementia Rating (CDR) of 0.5 with a Memory Box score of >=0.5;

3. Evidence of sleep complaints with Pittsburgh Sleep Quality Index score of >5 (a
well-validated cutoff observed in >40% of older persons);

4. Memory performance > 1.5 Standard Deviation (SD) below age-and education-matched
control subjects on the Repeatable Battery for the Assessment of Neuropsychological
Status (RBANS) List Recall;

5. Visual and auditory acuity adequate for neuropsychological testing;

6. Good general health with no disease expected to interfere with the study;

7. Able to have Magnetic Resonance Imaging (MRI) scan;

8. Availability of knowledgeable informant (KI)

Exclusion Criteria:

1. Less than 55 years of age to reduce likelihood of including individuals with
frontotemporal dementia or non-dementia MCI;

2. Too frail or medically unstable to undergo study procedures;

3. Prior diagnosis of Obstructive Sleep Apnea (OSA) or evidence of moderate-to-severe OSA
on baseline Home Sleep Test (HST) as evidenced by an apnea/hypopnea index of >15;

4. Dementia;

5. Cognitive complaints and deficits better explained by other medical/neurologic
conditions;

6. Delirium;

7. Allergic to trazodone;

8. Taking sleep medications including trazodone;

9. Current substance abuse;

10. Current major depressive, manic, or acute psychotic episode;

11. Prior diagnosis of significant systemic illness or unstable medical condition which
could lead to difficulty complying with the study protocol or represent alternate
primary cause of memory problems beyond Alzheimer's Disease (AD) pathology:

12. Lack of available KI;

13. Prior diagnosis of Q wave T wave Corrected for heart rate (QTc) > 470 msec (females)
or > 450 msec (males);

14. Inability to provide informed consent