Centre- Versus Home-based Exercise for MCI and Early Dementia (CHIME)
Primary Purpose
Mild Cognitive Impairment, Dementia
Status
Completed
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Centre-based exercise
Home-based exercise
Sponsored by

About this trial
This is an interventional treatment trial for Mild Cognitive Impairment
Eligibility Criteria
Inclusion Criteria:
- Diagnosis of MCI or mild dementia
- Mini-Mental State Examination (MMSE)>=23 or Montreal Cognitive Assessment (MoCA)>=18
- 50 years or older
- Stable pharmaceutical regimen >=2 months
- Be able to travel to centre
- Have a care partner or significant other to support home-based exercise
- Ability to walk >=2 minutes
- Adequate English to understand exercise training
- Adequate hearing and vision for cognitive tests
- Able to comply with assessment and training schedule
- Be screened safe for exercise by a physician or certified exercise physiologist
Exclusion Criteria:
- Current moderate or high intensity exercise >=3 times per week
- Unstable cardiovascular disease that precludes exercise
- Musculoskeletal impairments that limit ability to walk
- Pain or other co-morbidities that would limit exercise
- Behavioural issues that would limit exercise training
Sites / Locations
- Sunnybrook Research Institute
- University of Waterloo
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Centre-based physical activity
Home-based exercise
Arm Description
People with Mild Cognitive Impairment (MCI) and early dementia will receive centre-based physical activity for one hour each week for three months, plus at-home prescribed exercise.
People with Mild Cognitive Impairment (MCI) and early dementia be prescribed at-home prescribed exercise and will received monthly support phone calls.
Outcomes
Primary Outcome Measures
Achievement of Physical Activity
Percent achievement of physical activity recommendations (150min/wk of moderate or high intensity physical activity) as objectively measured using an activity monitor.
Change in physical activity
Change in physical activity as objectively measured using an activity monitor.
Secondary Outcome Measures
Cost-effectiveness
Cost of resource utilization per minute change in physical activity.
Full Information
NCT ID
NCT02774720
First Posted
April 7, 2016
Last Updated
May 27, 2019
Sponsor
University of Waterloo
Collaborators
Alzheimer's Association
1. Study Identification
Unique Protocol Identification Number
NCT02774720
Brief Title
Centre- Versus Home-based Exercise for MCI and Early Dementia
Acronym
CHIME
Official Title
How do we Get People With MCI and Dementia to be Physically Active?
Study Type
Interventional
2. Study Status
Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
September 2016 (undefined)
Primary Completion Date
March 2019 (Actual)
Study Completion Date
March 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Waterloo
Collaborators
Alzheimer's Association
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The study is a proof-of-concept, double-blinded randomized, parallel group trial to compare the effectiveness of centre-based and home-based physical activity in helping people with MCI and early dementia meet physical activity recommendations. The primary outcome is achievement of physical activity recommendations. Secondary outcomes include cost-effectiveness and improvements in health and function.
Detailed Description
The aim of this trial is to compare the effectiveness of center-based versus home-based physical activity delivery among people with MCI and early dementia and to understand the influence of person and setting characteristics.
OBJECTIVES:
Primary: To compare the effectiveness of centre-based versus home-based physical activity delivery among people with MCI or early dementia, as measured by percent achievement of physical activity guidelines.
Secondary:
(i) To determine the influence of person- and setting-specific factors. (ii) To estimate the cost-effectiveness of centre-based and home-based physical activity.
Exploratory:
i) To compare the effect of centre- and home-based physical activity on other outcomes.
ii) To explore whether participants consider certain aspects of the program to be important to program effectiveness.
METHODS:
The investigators will conduct a 3-month proof-of-concept, double-blinded randomized, parallel group trial to compare the effectiveness of centre-based and home-based physical activity in helping people with MCI and early dementia meet physical activity recommendations.
Participants will be randomized to one of two physical activity delivery options.The goal of both arms will be to have participants reach physical activity guidelines by the end of the 3-month intervention.
Participants who are randomized to centre-based physical activity will attend physical activity programming at a centre (University of Waterloo or Toronto Rehabilitation Institute) once per week for one hour. Additional physical activity will be prescribed at home.
Participants who are randomized to the home-based physical activity will received a physical activity prescription to be completed at home. They will also receive monthly support calls to assess achievements and barriers and to adjust the prescription.
All assessors will be blinded to group allocation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mild Cognitive Impairment, Dementia
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
44 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Centre-based physical activity
Arm Type
Experimental
Arm Description
People with Mild Cognitive Impairment (MCI) and early dementia will receive centre-based physical activity for one hour each week for three months, plus at-home prescribed exercise.
Arm Title
Home-based exercise
Arm Type
Experimental
Arm Description
People with Mild Cognitive Impairment (MCI) and early dementia be prescribed at-home prescribed exercise and will received monthly support phone calls.
Intervention Type
Behavioral
Intervention Name(s)
Centre-based exercise
Intervention Description
Participants will come to a centre (University of Waterloo or Toronto Rehabilitation Institute) for a one-hour, small group exercise class each week. The classes will include progressive aerobic and resistance exercise. They will be prescribed additional exercise to be performed independently (either at home or in the community).
Intervention Type
Behavioral
Intervention Name(s)
Home-based exercise
Intervention Description
Participants will be prescribed aerobic and resistance exercise to be performed independently (either at home or in the community). They will receive monthly phone calls to discuss achievements and barriers and to tje adjust exercise prescription.
Primary Outcome Measure Information:
Title
Achievement of Physical Activity
Description
Percent achievement of physical activity recommendations (150min/wk of moderate or high intensity physical activity) as objectively measured using an activity monitor.
Time Frame
3 months
Title
Change in physical activity
Description
Change in physical activity as objectively measured using an activity monitor.
Time Frame
baseline to 3 months
Secondary Outcome Measure Information:
Title
Cost-effectiveness
Description
Cost of resource utilization per minute change in physical activity.
Time Frame
3 months
Other Pre-specified Outcome Measures:
Title
Change in cognitive function as characterized by Alzheimer's Disease Assessment Scale - Cognition (ADAS-Cog)
Description
Change in continuous scores
Time Frame
baseline to 3 months
Title
Change in cognitive function as characterized by the Stroop task
Description
Change in continuous scores
Time Frame
baseline to 3 months
Title
Change in cognitive function as characterized by the Trail making task
Description
Change in continuous scores
Time Frame
baseline to 3 months
Title
Change in cognitive function as characterized by the semantic fluency
Description
Change in continuous scores
Time Frame
baseline to 3 months
Title
Change in physical function as characterized by the Short Physical Performance Battery (SPPB) scores
Description
Change in continuous scores
Time Frame
baseline to 3 months
Title
Change in quality of life as measured with the EuroQol five dimensions questionnaire (EQ-5D)
Description
Change in continuous scores
Time Frame
baseline to 3 months
Title
Change in mood as measured with the Neuropsychiatric Inventory Questionnaire (NPI-Q) (depression/dysphoria, anxiety, apathy/indifference scales)
Description
Change in scores, number meeting screening criteria for depression
Time Frame
baseline to 3 months
Title
Change in daily function as characterized using the 6-item Disability Assessment for Dementia (DAD-6)
Description
Change in score
Time Frame
baseline to 3 months
Title
Change in body mass index (BMI)
Description
Change in score
Time Frame
baseline to 3 months
Title
Change in waist circumference
Description
Change in score
Time Frame
baseline to 3 months
Title
Change in blood pressure
Description
Change in number with high blood pressure (>140 systolic blood pressure (SBP), >90 diastolic blood pressure (DBP))
Time Frame
baseline to 3 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosis of MCI or mild dementia
Mini-Mental State Examination (MMSE)>=23 or Montreal Cognitive Assessment (MoCA)>=18
50 years or older
Stable pharmaceutical regimen >=2 months
Be able to travel to centre
Have a care partner or significant other to support home-based exercise
Ability to walk >=2 minutes
Adequate English to understand exercise training
Adequate hearing and vision for cognitive tests
Able to comply with assessment and training schedule
Be screened safe for exercise by a physician or certified exercise physiologist
Exclusion Criteria:
Current moderate or high intensity exercise >=3 times per week
Unstable cardiovascular disease that precludes exercise
Musculoskeletal impairments that limit ability to walk
Pain or other co-morbidities that would limit exercise
Behavioural issues that would limit exercise training
Facility Information:
Facility Name
Sunnybrook Research Institute
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N 3M5
Country
Canada
Facility Name
University of Waterloo
City
Waterloo
State/Province
Ontario
ZIP/Postal Code
N2L3G1
Country
Canada
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Citations:
PubMed Identifier
29370756
Citation
Middleton LE, Black SE, Herrmann N, Oh PI, Regan K, Lanctot KL. Centre- versus home-based exercise among people with mci and mild dementia: study protocol for a randomized parallel-group trial. BMC Geriatr. 2018 Jan 25;18(1):27. doi: 10.1186/s12877-017-0684-0.
Results Reference
derived
Learn more about this trial
Centre- Versus Home-based Exercise for MCI and Early Dementia
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