NIA_Improving Function and Well-being by Improving Patient Memory: Transdiagnostic Sleep and Circadian Treatment (NCT05986604)
NIA_Improving Sleep and Circadian Functioning, Daytime Functioning, and Well-being for Midlife and Older Adults by Improving Patient Memory for a Transdiagnostic Sleep and Circadian Treatment
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: University of California, Berkeley — Berkeley, California
Age range: 50 Years
🧪 Interventions in This Study
- Memory Support Intervention (BEHAVIORAL)
- Transdiagnostic Intervention for Sleep and Circadian Dysfunction (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- University of California, Berkeley — Berkeley, California
📞 Contact the Study Coordinator
Phone: (510) 642-7138
Email: aharvey@berkeley.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Sleep Disorder
- Improving Sleep in a Psychiatric Hospital — Houston, Texas
- A Prospective Study to Evaluate the WP in Comparison to PSG in Patients Suspected of Sleep Disorders — Baltimore, Maryland
- Pilot Study of BCAA on Sleep — Portland, Oregon
Explore by condition: All Sleep Disorder clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.