Clinical trial Recruiting at 1 site Interventional Ages 55 and up

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.

More Alzheimer's Disease trials

Quick facts

Study typeInterventional
Ages55 Years and up
SexAll
Enrollment30 (estimated)
SponsorNorthwestern University
Academic / other
Locations1 site (Chicago, Illinois)
StatusRecruiting
StartedFebruary 2, 2026
Main results expectedDecember 15, 2026
Study endsDecember 15, 2026
Registry record updatedAugust 20, 2026
Trial IDNCT07775625 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

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.