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The Effect of Auditory Interventions on Anxiety and Agitation in People With Dementia

Primary Purpose

Mild to Moderate Dementia

Status
Recruiting
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Music and Theta Auditory Beat Stimulation
Audiobooks
Sponsored by
Lucid, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Mild to Moderate Dementia

Eligibility Criteria

65 Years - 85 Years (Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Mild to Moderate Dementia (mild: Montreal Cognitive Assessment (MOCA) scores (18-25); moderate: MOCA scores (10-17))) Exclusion Criteria: Unmanaged hearing loss (defined as average pure-tone average threshold of 35 dB HL or greater without the use of hearing instruments or personal sound amplification product) Severe Tinnitus Hyperacusis

Sites / Locations

  • LUCID TherapeuticsRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Music and Theta Auditory Beat Stimulation (ABS)

Audiobooks

Arm Description

Participants listen to 30 minutes of personalized music with theta auditory beat stimulation (ABS).

Participants listen to a 30-minute audiobook.

Outcomes

Primary Outcome Measures

Cohen Mansfield Agitation Index
The purpose of this scale is to assess the frequency of manifestations of agitated behaviors in elderly persons. Minimum score: 14, Maximum score: 70. Higher score indicates a worse outcome (increased agitation).

Secondary Outcome Measures

Rating of Anxiety in Dementia
A rating scale to measure anxiety in those that suffer from dementia. Minimum value: 0, Maximum value: 54. Higher score indicates worse outcome (increased anxiety)
Cornell Brown Scale for Quality of Life in Dementia
A scale that measures the quality of life of dementia patients. Minimum score: -38. Maximum score: 38. Higher score indicates better outcome (increased quality of life)
Zarit Caregiver Burden Interview
A scale that measures the caregiver burden of those that care for people with dementia and other ailments. Minimum score: 0, Maximum score: 88, Higher score indicates a worse outcome (higher caregiver burden).
Positive and Negative Affect Scale
The positive and negative affect scale is a good measure of a person's current mood. This scale generates two scores: 1) Positive affect (a higher score indicates a better outcome), scores range from 10-50. 2) Negative affect (higher score indicates worse outcome), scores range from 10-50.
Overt Agitation Severity Scale
A scale that identifies and measures the severity of agitated behavior in those with dementia/Alzheimer's disease. Minimum score: 0, Maximum score: 48. Higher score indicates a worse outcome (higher agitation symptoms).
Digit Span Forward
A cognitive measure of working memory.

Full Information

First Posted
April 10, 2023
Last Updated
May 9, 2023
Sponsor
Lucid, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT05844241
Brief Title
The Effect of Auditory Interventions on Anxiety and Agitation in People With Dementia
Official Title
The Effect of Auditory Interventions on Anxiety and Agitation in People With Dementia
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
May 8, 2023 (Actual)
Primary Completion Date
June 2023 (Anticipated)
Study Completion Date
July 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Lucid, Inc.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The greying of the world is leading to a rapid acceleration in both the healthcare costs and caregiver burden that are associated with dementia. There is an urgent need to develop new, easily scalable modalities of support to reduce agitation and anxiety in those with dementia. There is evidence that music interventions reduce agitation and anxiety in those with dementia. LUCID has developed a novel digital music therapeutic product that uses a reinforcement learning AI agent to curate and personalize the musical playlist while incorporating binaural theta auditory beat stimulation (ABS) to reduce anxiety and agitation in those with dementia. This study will be conducted remotely with study hardware (tablets and Bluetooth speakers) being shipped to caregivers/participants' homes. The study will take place over a 2-week period, with participants completing 4 one-hour sessions per week along with an additional 1-hour follow-up interview session. Forty-eight participants with mild to moderate dementia (as defined by the Montreal Cognitive Assessment) will be evenly randomized to one of two conditions. The control condition consists of a selection of 30-minute audiobooks which the participant has the freedom to select from. The experimental condition consists of music and binaural ABS curated by LUCID's AI system. Participants' caregivers will complete baseline questionnaires assessing the participants' anxiety, agitation, and mood. They will also complete these questionnaires before and after each experimental session. The investigators hypothesize that the LUCID AI music curation system will have a greater agitation and anxiety reduction compared to the audiobook control condition.
Detailed Description
The greying of the world is leading to a rapid acceleration in both the healthcare costs and caregiver burden that are associated with dementia. There is an urgent need to develop new, easily scalable modalities of support to reduce agitation and anxiety in those with dementia. There is evidence that music interventions reduce agitation and anxiety in those with dementia. LUCID has developed a novel digital music therapeutic product that uses a reinforcement learning AI agent to curate and personalize the musical playlist while incorporating binaural theta auditory beat stimulation (ABS) to reduce anxiety and agitation in those with dementia. This study will be conducted remotely with study hardware (tablets and Bluetooth speakers) being shipped to caregivers/participants' homes. The study will take place over a 2-week period, with participants completing 4 one-hour sessions per week along with an additional 1-hour follow-up interview session. Forty-eight participants with mild to moderate dementia (as defined by the Montreal Cognitive Assessment) will be evenly randomized to one of two conditions. The control condition consists of a selection of 30-minute audiobooks which the participant has the freedom to select from. The experimental condition consists of music and binaural ABS curated by LUCID's AI system. Participants' caregivers will complete baseline questionnaires assessing the participants' anxiety, agitation, and mood. They will also complete these questionnaires before and after each experimental session. Participants and their caregivers will schedule a Zoom call with a Research Assistant (RA) to assist them during their first onboarding session and go over study expectations and participants' rights. Participants/caregivers have access to and the ability to communicate and schedule meetings with RAs at any time should any issues arise over the course of the study. The investigators hypothesize that the LUCID AI music curation system will have a greater agitation and anxiety reduction compared to the audiobook control condition.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mild to Moderate Dementia

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
48 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Music and Theta Auditory Beat Stimulation (ABS)
Arm Type
Experimental
Arm Description
Participants listen to 30 minutes of personalized music with theta auditory beat stimulation (ABS).
Arm Title
Audiobooks
Arm Type
Active Comparator
Arm Description
Participants listen to a 30-minute audiobook.
Intervention Type
Other
Intervention Name(s)
Music and Theta Auditory Beat Stimulation
Intervention Description
Listening to music and ABS for 30 minutes.
Intervention Type
Other
Intervention Name(s)
Audiobooks
Intervention Description
Listening to audiobooks for 30 minutes
Primary Outcome Measure Information:
Title
Cohen Mansfield Agitation Index
Description
The purpose of this scale is to assess the frequency of manifestations of agitated behaviors in elderly persons. Minimum score: 14, Maximum score: 70. Higher score indicates a worse outcome (increased agitation).
Time Frame
2 weeks
Secondary Outcome Measure Information:
Title
Rating of Anxiety in Dementia
Description
A rating scale to measure anxiety in those that suffer from dementia. Minimum value: 0, Maximum value: 54. Higher score indicates worse outcome (increased anxiety)
Time Frame
2 weeks
Title
Cornell Brown Scale for Quality of Life in Dementia
Description
A scale that measures the quality of life of dementia patients. Minimum score: -38. Maximum score: 38. Higher score indicates better outcome (increased quality of life)
Time Frame
2 weeks
Title
Zarit Caregiver Burden Interview
Description
A scale that measures the caregiver burden of those that care for people with dementia and other ailments. Minimum score: 0, Maximum score: 88, Higher score indicates a worse outcome (higher caregiver burden).
Time Frame
2 weeks
Title
Positive and Negative Affect Scale
Description
The positive and negative affect scale is a good measure of a person's current mood. This scale generates two scores: 1) Positive affect (a higher score indicates a better outcome), scores range from 10-50. 2) Negative affect (higher score indicates worse outcome), scores range from 10-50.
Time Frame
30 minutes
Title
Overt Agitation Severity Scale
Description
A scale that identifies and measures the severity of agitated behavior in those with dementia/Alzheimer's disease. Minimum score: 0, Maximum score: 48. Higher score indicates a worse outcome (higher agitation symptoms).
Time Frame
30 minutes
Title
Digit Span Forward
Description
A cognitive measure of working memory.
Time Frame
30 minutes

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Mild to Moderate Dementia (mild: Montreal Cognitive Assessment (MOCA) scores (18-25); moderate: MOCA scores (10-17))) Exclusion Criteria: Unmanaged hearing loss (defined as average pure-tone average threshold of 35 dB HL or greater without the use of hearing instruments or personal sound amplification product) Severe Tinnitus Hyperacusis
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Adiel Mallik, PhD
Phone
514-835-8514
Email
adiel@thelucidproject.ca
First Name & Middle Initial & Last Name or Official Title & Degree
Rhiannon Ueberholz, BSc
Phone
416-357-5321
Email
rhiannon@thelucidproject.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Adiel Mallik, PhD
Organizational Affiliation
Lucid, Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
LUCID Therapeutics
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5C 1K9
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rhiannon Ueberholz, BSc
Email
rhiannon@thelucidproject.ca

12. IPD Sharing Statement

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The Effect of Auditory Interventions on Anxiety and Agitation in People With Dementia

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