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Effect of Soundscape on People With Dementia.

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ClinicalTrials.gov Identifier: NCT04809545
Recruitment Status : Recruiting
First Posted : March 22, 2021
Last Update Posted : April 28, 2021
Sponsor:
Collaborators:
University Ghent
University of Toronto
Information provided by (Responsible Party):
University Health Network, Toronto

Brief Summary:

In the last few decades, insights into the impact of the sonic environment on persons have grown to include not only the adverse effects of extensive mechanical noise but also the beneficial effects of a well-designed sonic environment. People with dementia, however, perceive and understand the sonic environment differently. The most obvious difference is that the meanings they may give to the sounds they notice due to changing mental associations. However, also at an earlier perceptual stage, attention focusing and gating may be affected, reducing their ability to analyze a complex auditory scene. Behaviour associated with the appraisal of the sound environment may change with the emergence of dementia.

The objective of this study is to determine the effect size of a carefully tuned personalized sonic environment (delivered via AcustiCare) on agitation and distress (NPI and PAS), night sleep and stress (Via wristband) and on quality of life (QUALIDEM) in a population of older adults with dementia and behavioural symptoms.


Condition or disease Intervention/treatment Phase
Dementia Behavioural and Psychiatric Symptoms of Dementia Other: Acusticare Other: Treatment as usual Not Applicable

Detailed Description:

Research has shown the positive effect of natural and non-natural soundscape on people with severe or profound intellectual disabilities (Andringa & van den Bosch, 2013). Sound plays a role in generating a feeling of safety, in influencing the mood, and triggering a specific action. Bringing sound with this purpose, as targeted to the current activity can improve the behaviour. There is substantial research on the effect of noise (unwanted sound) on people's health and well-being. The health outcomes vary, but include cardiovascular disease, sleep disturbance, and annoyance.

In a previous study in people with dementia by the Belgian investigators in this study (Devos et al., 2019), they observed positive staff outcome measures, reflecting the value of the soundscape in improving their ability to provide care to people with dementia. They did not directly assess the benefits to residents in that study. There were no harms documented in the study, and if residents reacted not well to specific sound, the sound was removed from the soundscape.

The aim of this study is to build upon the previous research and evaluate the effect of a personalized soundscape on the well-being and behaviour of persons with dementia. In the soundscapes, we use only recognizable sounds, sounds that give persons with dementia a feeling of 'safety' or sounds that focus on the orientation (in time, place). We try to add a recognizable (safe, orientating) sound through the soundscape system. This soundscape supports the environment and makes the environment feel safer and more 'clear' for residents with dementia. In the previous research through co-design process with staff and family member the sounds were chosen (Devos et al, 2018).

Most of the existing studies in the field of the acoustic environment in health care are descriptive, and there is a need for a more rigorous evaluation of interventions. By using a pilot Randomized Control Trial (RCT) design, we will be able to establish the effect size of soundscape on outcomes of interest in this population of people with dementia. These results will support evidence-based practices by healthcare providers, architects, engineers and designers in implementing environmental health factors and designing better care facilities for people with dementia in the future.

The objective of this study is thus to determine the effect size of a carefully tuned personalized sonic environment (delivered via AcustiCare) on agitation and distress (NPI and PAS), night sleep and stress (Via wristband) and on quality of life (QUALIDEM).

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Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 50 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Intervention Model Description: Single blind repeated-measures randomized controlled study with two parallel arms, Intervention and Treatment As Usual (TAU) with a 2:4:1 design (two baseline measures, four intervention measures, 1 post-intervention)
Masking: Double (Investigator, Outcomes Assessor)
Masking Description: Single-blind study where the intervention is delivered outside of the hours of the investigator and outcomes assessor.
Primary Purpose: Supportive Care
Official Title: Evaluation of Personalized Soundscape Effects on Persons With Dementia; a Pilot Randomized Clinical Trial
Actual Study Start Date : April 21, 2021
Estimated Primary Completion Date : April 1, 2022
Estimated Study Completion Date : April 1, 2022

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Dementia

Arm Intervention/treatment
Experimental: Intervention
The study intervention consists of the delivery of a soundscape in the private rooms of the participant during the morning and evening. The soundscape is personalized and consists of a collection of natural sounds, birdsongs, kitchen sounds, music, bell sound, outdoor sounds, water/rain sounds, and similar.
Other: Acusticare
Acusticare is an internet connected speaker which delivers an environmental intervention by playing sounds to adjust the soundscape in the room.

Active Comparator: Treatment as Usual
As part of usual care, patients on the Specialized Dementia Unit receive a comprehensive assessment of their health and symptoms of dementia involving consultation by a geriatric psychiatrist, geriatrician, physical therapist, occupational therapist, and recreation therapist, and pharmacological and non-pharmacological treatment plans are developed and executed. All participants in the study will receive this standard of care
Other: Treatment as usual
Usual care provided on the Specialized Dementia Unit




Primary Outcome Measures :
  1. Change over 6 weeks in Neuropsychiatric Inventory- total score [ Time Frame: Baseline and weekly over 6 weeks ]
    Assessments of behavioural and psychological symptoms of dementia on a weekly basis over the study duration will be included in a longitudinal mixed effects model as part of a repeated measures design


Secondary Outcome Measures :
  1. Change over 6 weeks in the Pittsburgh Agitation Scale-- Resisting Care subscale [ Time Frame: Baseline and weekly over 6 weeks ]
    Assessment of resistance to care on a weekly basis over the study duration will be included in a longitudinal mixed effects model as part of a repeated measures design

  2. Change over 6 weeks in the Pittsburgh Agitation Scale-- Total score [ Time Frame: Baseline and weekly over 6 weeks ]
    Assessment of behavioural symptoms on a weekly basis over the study duration will be included in a longitudinal mixed effects model as part of a repeated measures design

  3. Change over 6 weeks in Neuropsychiatric Inventory Agitation Subscale [ Time Frame: Baseline and weekly over 6 weeks ]
    Assessment of agitation on a weekly basis over the study duration will be included in a longitudinal mixed effects model as part of a repeated measures design

  4. Change over 6 weeks in Neuropsychiatric Inventory Aggression subscale [ Time Frame: Baseline and weekly over 6 weeks ]
    Assessment of aggression on a weekly basis over the study duration will be included in a longitudinal mixed effects model as part of a repeated measures design

  5. Change over 6 weeks in Neuropsychiatric Inventory Dysphoria subscale [ Time Frame: Baseline and weekly over 6 weeks ]
    Assessment of dysphoria on a weekly basis over the study duration will be included in a longitudinal mixed effects model as part of a repeated measures design

  6. Change in Neuropsychiatric Inventory Anxiety subscale [ Time Frame: Baseline and weekly over 6 weeks ]
    Assessment of anxiety on a weekly basis over the study duration will be included in a longitudinal mixed effects model as part of a repeated measures design

  7. Change in Qualidem [ Time Frame: Baseline, Week 6 ]
    Dementia-related quality of life


Other Outcome Measures:
  1. Change in staff feedback on 5-point scale over 6 weeks [ Time Frame: Baseline and daily over 6 weeks ]
    Staff can provide real-time feedback on a daily basis on resident mood and behaviour using a 5-button scale

  2. Change in accelerometer-measured nocturnal activity level over time [ Time Frame: Weeks 2,4,5 and 6 ]
    Using an accelerometer, will assess activity levels overnight as a measure of sleep fragmentation

  3. Change in heart rate variability over time [ Time Frame: Weeks 2,4,5 and 6 ]
    Heart rate variability as a measure of stress



Information from the National Library of Medicine

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Ages Eligible for Study:   65 Years and older   (Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. 65 years or older
  2. Diagnosis of Dementia
  3. Symptoms of BPSD at baseline
  4. English speaking
  5. Assigned a private room with AcustiCare installed

Exclusion Criteria:

  1. Severe hearing impairment
  2. Receiving end-of-life care

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04809545


Contacts
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Contact: Andrea Iaboni, MD DPhil 416-597-3422 ext 3027 andrea.iaboni@uhn.ca
Contact: Alastair Flint, MD 416-340-4788 alastair.flint@uhn.ca

Locations
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Canada, Ontario
Toronto Rehabilitation Institute, University Health Network Recruiting
Toronto, Ontario, Canada, M5G2A2
Contact: Andrea Iaboni    416-597-3422 ext 3027    andrea.iaboni@uhn.ca   
Principal Investigator: Andrea Iaboni, MD DPhil         
Sponsors and Collaborators
University Health Network, Toronto
University Ghent
University of Toronto
Investigators
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Principal Investigator: Andrea Iaboni, MD DPhil University Health Network, Toronto
Publications:
Devos, P., Aletta, F., Vander Mynsbrugge, T., Thomas, P., Filipan, K., Petrovic, M., ... & Botteldooren, D. (2018, December). Soundscape design for management of behavioral disorders: a pilot study among nursing home residents with dementia. In INTER-NOISE and NOISE-CON Congress and Conference Proceedings (Vol. 258, No. 5, pp. 2104-2111). Institute of Noise Control Engineerin

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Responsible Party: University Health Network, Toronto
ClinicalTrials.gov Identifier: NCT04809545    
Other Study ID Numbers: 20-5067
First Posted: March 22, 2021    Key Record Dates
Last Update Posted: April 28, 2021
Last Verified: March 2021
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

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Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Keywords provided by University Health Network, Toronto:
Soundscape
Sonic environment
Neuropsychiatric symptoms
Dementia
Environmental design
Additional relevant MeSH terms:
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Dementia
Alzheimer Disease
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Neurocognitive Disorders
Mental Disorders
Tauopathies
Neurodegenerative Diseases