Central Auditory Processing Modulation Underlying Anxiety Reduction Using Clinically Designed Improvisatory Music

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age55+
SponsorNorthwestern University

About this trial

This study examines whether Clinically Designed Improvisatory Music (CDIM) can reduce anxiety in people living with Alzheimer's disease and anxiety (AD-A), and whether it can also lessen caregiver burden. CDIM is a live, receptive music-based intervention that uses slow tempi, simple diatonic melodic lines, soft dynamics, and periodic pauses to promote relaxation. As described in the proposal, CDIM has previously been shown to reduce stress and improve physiological markers such as heart rate, blood pressure, and EEG alpha/beta ratios (CDIM significantly decreased physical stress symptoms and patients also reported positive emotional outcomes and EEG readings showed increased alpha/beta brainwave ratios ).

The study will enroll 30 dyads (individuals with AD-A and their caregivers). Dyads will be randomly assigned to either CDIM or a control intervention (CI) consisting of calming short stories read aloud. Both interventions include eight 30-minute sessions over four weeks, delivered in alternating in-person and virtual formats.

The primary goal is to determine whether CDIM is feasible and effective in reducing anxiety in individuals with AD-A, measured by the Rating Anxiety in Dementia (RAID) scale, and in reducing caregiver burden, measured by the Zarit Burden Interview (ZBI). The study also evaluates changes in heart rate and blood pressure as indicators of autonomic regulation.

A second goal is to explore whether CDIM improves central auditory processing, assessed using the frequency-following response (FFR). The proposal notes that central auditory processing declines with age and dementia and may contribute to anxiety. FFR will be measured before and after the intervention to determine whether CDIM enhances neural timing and response magnitude.

Overall, this pilot study aims to determine whether CDIM is a feasible, safe, and potentially effective non-pharmacological intervention for reducing anxiety in individuals with AD-A and decreasing caregiver burden, while also investigating its underlying neurophysiological mechanisms.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Significant hearing impairments

Major comorbidities Beck Depression Inventory (BDI) scores above > 10'

Trial design

Design model

Single group

Treatments tested in this trial

  • Clinically Designed Improvisatory Music

    Other intervention

    Clinically Designed Improvisatory Music (CDIM) is live, slow-tempo, diatonic improvisation played with soft dynamics and periodic pauses. It uses meterless melodic lines, vocal-range pitches, and gentle harmonic intervals to promote neural entrainment, parasympathetic activation, and anxiety reduction in listeners.

  • Listening to Storytelling

    Other intervention

    Participants will listen to calming short stories within 30 minutes.

Treatment groups

30 Participants
are divided into 2 treatment groups
Group A: Clinically Designed Improvisatory MusicExperimental treatment 1 intervention
Group B: Listening to storytellingActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Rating Anxiety in Dementia (RAID)

RAID is a structured clinical scale measuring anxiety in dementia. It will be evaluated 3 times, 4 weeks apart.

Time frame
From enrollment to the end of treatment at 8 weeks.

Secondary outcomes

1

Frequency Following Response (FFR)

FFR is a scalp-recorded neural measure capturing precise subcortical encoding of sound timing, frequency, and speech acoustics.

Time frame
It will be evaluated at baseline and up to a week after intervention.
2

Heart rate

Heart rate per minute

Time frame
Measured at baseline up to a week after intervention.
3

Blood pressure

Blood pressure measured using a blood pressure machine.

Time frame
Measured at baseline up to a week after intervention.
4

Respiratory Rate

Number of respirations per minutes.

Time frame
Measured at baseline and up to a week after intervention.

Other outcomes

Sponsors and contacts

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