Music-based approach to reduce anxiety in Alzheimer's patients and support caregivers
Official title: Central Auditory Processing Modulation Underlying Anxiety Reduction Using Clinically Designed Improvisatory Music
Run by Northwestern University · NCT07775625 · Data updated 2026-11-12
This study tests whether Clinically Designed Improvisatory Music can lower anxiety in people with Alzheimer's and anxiety, and whether it eases caregiver burden.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 55 Years and up |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | Northwestern University Academic / other |
| Locations | 1 site (Chicago, Illinois) |
| Status | Recruiting |
| Started | February 2, 2026 |
| Main results expected | December 15, 2026 |
| Study ends | December 15, 2026 |
| Registry record updated | August 20, 2026 |
| Trial ID | NCT07775625 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are individuals with Alzheimer's disease and anxiety, confirmed biomarkers, MMSE ≥15, RAID >8, and able to participate with a caregiver.
✕Probably not a fit
Patients with significant hearing impairment, severe depression (BDI >10), or major comorbidities may not benefit or participate safely.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This randomized, dyad-focused trial compares Clinically Designed Improvisatory Music (CDIM) with a calming listening control over eight 30-minute sessions across four weeks. Participants are people with Alzheimer's disease and anxiety and their caregivers, enrolled as 30 patient–caregiver pairs. The intervention uses slow tempo, simple melodies, soft dynamics, and pauses to promote relaxation, and the control condition involves listening to calming short stories. Outcomes include changes in anxiety and caregiver burden, along with safety and feasibility measures. Eligibility requires confirmed Alzheimer's diagnosis with positive biomarkers, MMSE of 15 or higher, RAID score above 8, and no significant hearing loss or severe depression.
Why it matters
Potential benefit: If successful, CDIM could reduce anxiety for people with Alzheimer's and lessen caregiver burden.
How similar studies have gone: Previous work with CDIM showed reductions in stress markers and positive emotional outcomes, supporting further study in this population.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria * Clinical diagnosis of Alzheimer's Disease * Positive Alzheimer's disease biomarkers (blood test, amyloid PET scan or CSF) * Mini-mental State Exam (MMSE) \>=15 * Rating for Anxiety in Dementia (RAID) score \> 8 Exclusion Criteria * Significant hearing impairments * Major comorbidities Beck Depression Inventory (BDI) scores above \> 10'
Where it's running
-
Northwestern University Feinberg School of Medicine
Chicago, Illinois, United States Recruiting
Study contacts
- Study coordinator: Borna Bonakdarpour - Associate Professor, MD, FAAN, FANA
- Email: bbk@northwestern.edu
- Phone: (312) 503-5170
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.