Actively Recruiting
NIA_Improving Function and Well-being by Improving Patient Memory: Transdiagnostic Sleep and Circadian Treatment
Led by University of California, Berkeley · Updated on 2025-11-24
178
Participants Needed
1
Research Sites
238 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Mental illness is often chronic, severe, and difficult to treat. Though there has been significant progress towards establishing effective and efficient interventions for psychological health problems, many individuals do not gain lasting benefits from these treatments. The Memory Support Intervention (MSI) was developed utilizing existing findings from the cognitive science literature to improve treatment outcomes. In this study, the investigators aim to conduct an open trial that includes individuals 50 years and older to assess if a novel version of the Memory Support Intervention improves sleep and circadian functioning, reduces functional impairment, and improves patient memory for treatment.
CONDITIONS
Official Title
NIA_Improving Function and Well-being by Improving Patient Memory: Transdiagnostic Sleep and Circadian Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Aged 50 years and older
- Fluent in English
- Experiencing a mobility impairment
- Low income
- Reporting significant sleep or circadian disturbance by PROMIS-SD measure
- Scoring 25-30 on Montreal Cognitive Assessment indicating no cognitive impairment
- Able and willing to provide informed consent
You will not qualify if you...
- Severe untreated sleep disordered breathing (AHI > 30) or moderate untreated sleep disordered breathing with severe daytime sleepiness (AHI 15-30 and Epworth Sleepiness Scale > 10)
- Medical conditions preventing comprehension or participation (e.g., dementia, narcolepsy, REM sleep behavior disorder, end of life care)
- Homelessness
- Night shift work more than 2 nights per week in past 3 months
- Substance abuse or dependence if it prevents study participation
- Suicide risk that prevents outpatient treatment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of California, Berkeley
Berkeley, California, United States, 94720-1650
Actively Recruiting
Research Team
A
Allison Harvey, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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