- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06079216
Making Connections Thru Music (MCTM)
Making Connections Thru Music: A Group Music Therapy-Based Intervention for Persons With Dementia
Healthcare systems around the world, including within the United States, have long-established shortages of trained caregivers. The American Health Care Association states that "the health care system has experienced a shortage of trained caregivers for critical roles for some time." This scarcity directly impacts the 45,800 Long-Term Care (LTC) communities throughout the U.S.
Concurrent with this staff shortage, more than half of LTC residents have some form of dementia. These two issues create a serious public health concern, since dementia is associated with a variety of behavioral expressions, such as aggression, anxiety, and agitation. Behavioral expressions of dementia can be successfully managed with the use of tailored, psychosocial interventions and communication support. Unfortunately, existing staff shortages make the facilitation of such interventions challenging.
One powerful and often-overlooked approach to ameliorating staffing shortages involves the utilization of retired volunteers to facilitate interventions for persons with dementia (PWD). Based on the nearly universal love of music and a promising pilot study, the product to be developed and tested in this STTR will build upon the combined prior work of the Principal Investigators. Making Connections Thru Music (MCTM), an urgently needed product, will enable retired volunteers to facilitate an evidence-based music and discussion intervention with PWD. MCTM aims to improve engagement, enhance quality of life, and reduce behavioral expressions in PWD. The intervention will consist of two main components: (1) a comprehensive online training course for volunteers, which will provide a general overview of dementia, demonstrate effective communication strategies to use with PWD, and instruct volunteers to effectively facilitate MCTM sessions, and (2) an app containing a structured MCTM intervention protocol and toolkit, which will be the means by which volunteers facilitate MCTM. MCTM will be marketed to LTC communities.
Study Overview
Status
Conditions
Study Type
Enrollment (Estimated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Massachusetts
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Winchester, Massachusetts, United States, 01890
- The Hearthstone Institute, LLC
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Volunteers must be aged 55+ and speak/read conversational English.
- Staff participants must be at least 18 years old, work within a residential care facility participating in the study, and speak and read English.
Exclusion Criteria:
- Volunteers will be excluded if they are diagnosed with dementia based on self-report and/or if they score 23 or lower on theMini Mental State Exam (MMSE; Folstein et al., 1975). Such a score would be indicative of possible cognitive impairment.
- Staff members will be excluded if they work third shift only. PWD Residents with dementia must be diagnosed with dementia (any type), score 10 or above on the MMSE, be aged 65+, and speak/read conversational English.
- PWD will be excluded if they show signs of rapid physical or cognitive decline (based upon staff report or as evidenced by information gained during screening).
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: MCTM Intervention
Activity sessions will be led by activity volunteers
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Volunteer led Group music therapy-based intervention
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Active Comparator: Control
Activity sessions will be led by activity professionals
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Staff led Group music therapy-based intervention
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Menorah Park Engagement Scale
Time Frame: Baseline (weeks 1-4) Treatment (weeks 5-12)
|
The MPES is an observational scale that measures four types of engagement: Constructive Engagement, Passive Engagement, Distracted Engagement, and Non-Engagement / Apathy The MPES also measures Pleasure, defined as clearly observable smiling or laughing.
For each item, the minimum possible value is 0 (not at all) and the maximum possible value is 2 (more than half of the time).
For Constructive Engagement, Passive Engagement, and Pleasure, higher scores would represent a better outcome.
For Distracted Engagement and Non-Engagement, higher scores would represent a worse outcome.
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Baseline (weeks 1-4) Treatment (weeks 5-12)
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Alzheimer's Disease Knowledge Scale
Time Frame: Baseline (weeks 1-4) Treatment (weeks 5-12)
|
30-item scale to measure knowledge of Alzheimer's Disease.
The range of score is zero to 30.
A higher score indicates a better outcome.
|
Baseline (weeks 1-4) Treatment (weeks 5-12)
|
|
Geriatric Depression Scale- Short Form. Scores can range from zero to 15. Higher scores suggest a worse outcome
Time Frame: Baseline (weeks 1-4) Treatment (weeks 5-12)
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This is a 15-item measure of depression in older adults that is conducted via direct interview.
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Baseline (weeks 1-4) Treatment (weeks 5-12)
|
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Neuropsychiatric Inventory - Nursing Home.
Time Frame: Baseline (weeks 1-4) Treatment (weeks 5-12)
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The Neuropsychiatric Inventory-Nursing Home is a comprehensive assessment of psychopathology in persons with dementia, focused on people residing in nursing homes.
Researchers typically use the frequency x severity (FxS) total score on this measure.
We will be using this score in this study.
The FxS score ranges from 0 to 120, with a higher score indicating a worse outcome.
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Baseline (weeks 1-4) Treatment (weeks 5-12)
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Estimated)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Cerebrovascular Disorders
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Vascular Diseases
- Cardiovascular Diseases
- Mental Disorders
- Neurocognitive Disorders
- Tauopathies
- Neurodegenerative Diseases
- Arteriosclerosis
- Arterial Occlusive Diseases
- Leukoencephalopathies
- Intracranial Arteriosclerosis
- Intracranial Arterial Diseases
- Alzheimer Disease
- Dementia
- Dementia, Vascular
Other Study ID Numbers
- HearthstoneI
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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