- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05004558
Effects of Remote-based Resistance Training on Cardiometabolic Risk Factors, Cognitive Function, and Quality of Life in Adults Living With Alzheimer's Disease and/or Related Dementias
Effects of a 24-week Remote-based Resistance Training Program on Parameters of the Metabolic Syndrome, Cognitive Function, and Quality of Life in Older Adults Living With Mild Cognitive Impairment and Alzheimer's Disease and/or a Related Dementia
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The investigators aim to study the effects of a 24-week remote-based resistance exercise training program on cardiovascular disease risk factors, cognitive function, and quality of life in older adults living with mild cognitive impairment or Alzheimer's Disease and/or a related dementia. Data for this study will be collected at the beginning, middle, and end of the resistance training program. Measurements of resting blood pressure will be collected with an automated blood pressure monitor. Fasting blood glucose and lipids will be retrieved from the electronic medical record or from a finger stick. Waist and hip circumferences will be collected with a tape measure. Height and weight will be collected with a physician scale. Cognitive function and quality of life will be collected from interviews using the Montreal Cognitive Assessment and Short-Form (36) Health Survey. All data collected from this study will be de-identified using the "Safe-Harbor" method, which minimizes exposure of personal health information by providing each participant with a unique participant-ID and only providing access to those who are listed and approved for access privileges. Data collected for this study will also be stored on an encrypted and password- protected hard drive, and data analyzed will be performed with the Statistical Package for the Social Sciences using analyses of covariance.
When participants are enrolled in the study, he/she will be grouped on the basis of their cognitive function status from the Montreal Cognitive Assessment. All participants will then receive supervised remote-based resistance exercise training with Therabands, 3 days per week for 24 weeks. The risks of participating in exercise programs are minimal. Some of the possible risks of participating in resistance exercise include becoming tired and/or experiencing delayed onset muscle soreness, leg cramping, or muscle strain from performing resistance exercise. There are several benefits from engaging in resistance exercise programs. Participants of this study will receive health-fitness assessment at the beginning, middle, and end of the study, and as such, will benefit from being made aware of their cardiovascular disease risk factors, cognitive function, and quality of life. Other possible benefits from participation in the resistance exercise program may include improvements in muscular size and strength and/or activities of daily living.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 55 years of age or older
- Sedentary or not meeting the current physical activity guidelines of at least 150 minutes of moderate-to-vigorous physical activity per week
- Live with or have a primary in-home caregiver or legal representative who can be physically present during the remote-based exercise sessions
- Have access to a computer, tablet, or smartphone with internet and webcam access for the HIPAA compliant virtual Zoom meetings.
Exclusion Criteria:
- Younger than 55 years of age
- Accustomed to resistance exercise training during the previous year
- Live with known or suggestive uncontrolled cardiovascular, metabolic, and/or renal disease
- Live with musculoskeletal injury that precludes their ability to perform remote-based, resistance exercise training
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Remote-based Resistance Exercise Training
All participants enrolled in the trial will receive supervised remote-based resistance exercise training.
The exercises will be performed with the use of Therabands and will include 8-10 exercises performed for 1 set of 15 repetitions, performed 3 days per week for 24 weeks.
|
All participants enrolled in the trial will receive supervised remote-based resistance exercise training.
The exercises will be performed with the use of Therabands and will include 8-10 exercises performed for 1 set of 15 repetitions, performed 3 days per week for 24 weeks.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Resting systolic blood pressure, measured in mmHg from 0 and above with higher numbers indicating higher blood pressure
Time Frame: Baseline
|
Resting systolic blood pressure will be measured with an automated blood pressure device, measured in mmHg from 0 and above with higher numbers indicating higher blood pressure
|
Baseline
|
Resting systolic blood pressure, measured in mmHg from 0 and above with higher numbers indicating higher blood pressure
Time Frame: 12 weeks
|
Resting systolic blood pressure will be measured with an automated blood pressure device, measured in mmHg from 0 and above with higher numbers indicating higher blood pressure
|
12 weeks
|
Resting systolic blood pressure, measured in mmHg from 0 and above with higher numbers indicating higher blood pressure
Time Frame: 24 weeks
|
Resting systolic blood pressure will be measured with an automated blood pressure device, measured in mmHg from 0 and above with higher numbers indicating higher blood pressure
|
24 weeks
|
Resting diastolic blood pressure, measured in mmHg from 0 and above with higher numbers indicating higher blood pressure
Time Frame: Baseline
|
Resting diastolic blood pressure will be measured with an automated blood pressure device, measured in mmHg from 0 and above with higher numbers indicating higher blood pressure
|
Baseline
|
Resting diastolic blood pressure, measured in mmHg from 0 and above with higher numbers indicating higher blood pressure
Time Frame: 12 weeks
|
Resting diastolic blood pressure will be measured with an automated blood pressure device, measured in mmHg from 0 and above with higher numbers indicating higher blood pressure
|
12 weeks
|
Resting diastolic blood pressure, measured in mmHg from 0 and above with higher numbers indicating higher blood pressure
Time Frame: 24 weeks
|
Resting diastolic blood pressure will be measured with an automated blood pressure device, measured in mmHg from 0 and above with higher numbers indicating higher blood pressure
|
24 weeks
|
Height, red with a stadiometer in inches from 0 and above with higher numbers indicating taller height
Time Frame: Baseline
|
Height will be measured with a stadiometer in inches from 0 and above with higher numbers indicating taller height
|
Baseline
|
Height, red with a stadiometer in inches from 0 and above with higher numbers indicating taller height
Time Frame: 12 weeks
|
Height will be measured with a stadiometer in inches from 0 and above with higher numbers indicating taller height
|
12 weeks
|
Height, red with a stadiometer in inches from 0 and above with higher numbers indicating taller height
Time Frame: 24 weeks
|
Height will be measured with a stadiometer in inches from 0 and above with higher numbers indicating taller height
|
24 weeks
|
Weight, ured with a physican scale in pounds from 0 and above with higher numbers indicating heavier weight
Time Frame: Baseline
|
Weight will be measured with a physican scale in pounds from 0 and above with higher numbers indicating heavier weight
|
Baseline
|
Weight, ured with a physican scale in pounds from 0 and above with higher numbers indicating heavier weight
Time Frame: 12 weeks
|
Weight will be measured with a physican scale in pounds from 0 and above with higher numbers indicating heavier weight
|
12 weeks
|
Weight, ured with a physican scale in pounds from 0 and above with higher numbers indicating heavier weight
Time Frame: 24 weeks
|
Weight will be measured with a physican scale in pounds from 0 and above with higher numbers indicating heavier weight
|
24 weeks
|
Body mass index, measured in meters squared, from 0 and above wiith larger values indicating a higher body mass index
Time Frame: Baseline
|
Body mass index will be measured as the weight measured in kilograms divided by the height measured in meters squared, from 0 and above wiith larger values indicating a higher body mass index
|
Baseline
|
Body mass index, measured in meters squared, from 0 and above wiith larger values indicating a higher body mass index
Time Frame: 12 weeks
|
Body mass index will be measured as the weight measured in kilograms divided by the height measured in meters squared, from 0 and above wiith larger values indicating a higher body mass index
|
12 weeks
|
Body mass index, measured in meters squared, from 0 and above wiith larger values indicating a higher body mass index
Time Frame: 24 weeks
|
Body mass index will be measured as the weight measured in kilograms divided by the height measured in meters squared, from 0 and above wiith larger values indicating a higher body mass index
|
24 weeks
|
Waist circumference, red in inches with a Gulick tape measure from 0 and above with higher numbers indicating a larger waist circumference
Time Frame: Baseline
|
Waist circumference will be measured in inches with a Gulick tape measure from 0 and above with higher numbers indicating a larger waist circumference
|
Baseline
|
Waist circumference, red in inches with a Gulick tape measure from 0 and above with higher numbers indicating a larger waist circumference
Time Frame: 12 weeks
|
Waist circumference will be measured in inches with a Gulick tape measure from 0 and above with higher numbers indicating a larger waist circumference
|
12 weeks
|
Waist circumference, red in inches with a Gulick tape measure from 0 and above with higher numbers indicating a larger waist circumference
Time Frame: 24 weeks
|
Waist circumference will be measured in inches with a Gulick tape measure from 0 and above with higher numbers indicating a larger waist circumference
|
24 weeks
|
Hip circumference, sured in inches with a Gulick tape measure from 0 and above with higher numbers indicating a larger waist circumference
Time Frame: Baseline
|
Hip circumference will be measured in inches with a Gulick tape measure from 0 and above with higher numbers indicating a larger waist circumference
|
Baseline
|
Hip circumference, sured in inches with a Gulick tape measure from 0 and above with higher numbers indicating a larger waist circumference
Time Frame: 12 weeks
|
Hip circumference will be measured in inches with a Gulick tape measure from 0 and above with higher numbers indicating a larger waist circumference
|
12 weeks
|
Hip circumference, sured in inches with a Gulick tape measure from 0 and above with higher numbers indicating a larger waist circumference
Time Frame: 24 weeks
|
Hip circumference will be measured in inches with a Gulick tape measure from 0 and above with higher numbers indicating a larger waist circumference
|
24 weeks
|
Blood glucose, measured in mg/dL from 0 and above with larger values indicating a higher blood glucose concentration
Time Frame: Baseline
|
Blood glucose will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher blood glucose concentration
|
Baseline
|
Blood glucose, measured in mg/dL from 0 and above with larger values indicating a higher blood glucose concentration
Time Frame: 12 weeks
|
Blood glucose will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher blood glucose concentration
|
12 weeks
|
Blood glucose, measured in mg/dL from 0 and above with larger values indicating a higher blood glucose concentration
Time Frame: 24 weeks
|
Blood glucose will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher blood glucose concentration
|
24 weeks
|
High density lipoprotein cholesterol, ed in mg/dL from 0 and above with larger values indicating a higher high density lipoprotein concentrations, a desirable finding
Time Frame: Baseline
|
High density lipoprotein cholesterol will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher high density lipoprotein concentrations, a desirable finding
|
Baseline
|
High density lipoprotein cholesterol, ed in mg/dL from 0 and above with larger values indicating a higher high density lipoprotein concentrations, a desirable finding
Time Frame: 12 weeks
|
High density lipoprotein cholesterol will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher high density lipoprotein concentrations, a desirable finding
|
12 weeks
|
High density lipoprotein cholesterol, ed in mg/dL from 0 and above with larger values indicating a higher high density lipoprotein concentrations, a desirable finding
Time Frame: 24 weeks
|
High density lipoprotein cholesterol will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher high density lipoprotein concentrations, a desirable finding
|
24 weeks
|
Low density lipoprotein cholesterol, measured in mg/dL from 0 and above with larger values indicating a higher low density lipoprotein concentrations, an undesirable finding
Time Frame: Baseline
|
Low density lipoprotein cholesterol will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher low density lipoprotein concentrations, an undesirable finding
|
Baseline
|
Low density lipoprotein cholesterol, measured in mg/dL from 0 and above with larger values indicating a higher low density lipoprotein concentrations, an undesirable finding
Time Frame: 12 weeks
|
Low density lipoprotein cholesterol will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher low density lipoprotein concentrations, an undesirable finding
|
12 weeks
|
Low density lipoprotein cholesterol, measured in mg/dL from 0 and above with larger values indicating a higher low density lipoprotein concentrations, an undesirable finding
Time Frame: 24 weeks
|
Low density lipoprotein cholesterol will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher low density lipoprotein concentrations, an undesirable finding
|
24 weeks
|
Triglycerides, measured in mg/dL from 0 and above with larger values indicating a higher triglyceride concentrations, an undesirable finding
Time Frame: Baseline
|
Triglycerides will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher triglyceride concentrations, an undesirable finding
|
Baseline
|
Triglycerides, measured in mg/dL from 0 and above with larger values indicating a higher triglyceride concentrations, an undesirable finding
Time Frame: 12 weeks
|
Triglycerides will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher triglyceride concentrations, an undesirable finding
|
12 weeks
|
Triglycerides, measured in mg/dL from 0 and above with larger values indicating a higher triglyceride concentrations, an undesirable finding
Time Frame: 24 weeks
|
Triglycerides will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher triglyceride concentrations, an undesirable finding
|
24 weeks
|
Total cholesterol, measured in mg/dL from 0 and above with larger values indicating a higher total cholesterol concentrations, an undesirable finding
Time Frame: Baseline
|
Total cholesterol will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher total cholesterol concentrations, an undesirable finding
|
Baseline
|
Total cholesterol, measured in mg/dL from 0 and above with larger values indicating a higher total cholesterol concentrations, an undesirable finding
Time Frame: 12 weeks
|
Total cholesterol will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher total cholesterol concentrations, an undesirable finding
|
12 weeks
|
Total cholesterol, measured in mg/dL from 0 and above with larger values indicating a higher total cholesterol concentrations, an undesirable finding
Time Frame: 24 weeks
|
Total cholesterol will be measured with a Cholestech LDX analyzer via finger sticking, measured in mg/dL from 0 and above with larger values indicating a higher total cholesterol concentrations, an undesirable finding
|
24 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Cognitive Function as Measured by the Montreal Cognitive Assessment
Time Frame: Baseline
|
Cognitive function will be assessed with the Montreal Cognitive Assessment Screen, measured from 0 to 30 with higher scores indicating better cognitive function
|
Baseline
|
Cognitive Function as Measured by the Montreal Cognitive Assessment
Time Frame: 12 weeks
|
Cognitive function will be assessed with the Montreal Cognitive Assessment Screen, measured from 0 to 30 with higher scores indicating better cognitive function
|
12 weeks
|
Cognitive Function as Measured by the Montreal Cognitive Assessment
Time Frame: 24 weeks
|
Cognitive function will be assessed with the Montreal Cognitive Assessment Screen, measured from 0 to 30 with higher scores indicating better cognitive function
|
24 weeks
|
Quality of Life as measured by the Short-Form (36) Health Survey
Time Frame: Baseline
|
Quality of life will be assessed with the Short-Form (36) Health Survey, measured from 0 to 100 with higher scores indicating better quality of life
|
Baseline
|
Quality of Life as measured by the Short-Form (36) Health Survey
Time Frame: 12 weeks
|
Quality of life will be assessed with the Short-Form (36) Health Survey, measured from 0 to 100 with higher scores indicating better quality of life
|
12 weeks
|
Quality of Life as measured by the Short-Form (36) Health Survey
Time Frame: 24 weeks
|
Quality of life will be assessed with the Short-Form (36) Health Survey, measured from 0 to 100 with higher scores indicating better quality of life
|
24 weeks
|
Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Anticipated)
Primary Completion (Anticipated)
Study Completion (Anticipated)
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
- Mental Disorders
- Cardiovascular Diseases
- Vascular Diseases
- Metabolic Diseases
- Cerebrovascular Disorders
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Arteriosclerosis
- Arterial Occlusive Diseases
- Neurologic Manifestations
- Neurobehavioral Manifestations
- Neurocognitive Disorders
- Overnutrition
- Nutrition Disorders
- Overweight
- Parkinsonian Disorders
- Basal Ganglia Diseases
- Movement Disorders
- Synucleinopathies
- Neurodegenerative Diseases
- TDP-43 Proteinopathies
- Proteostasis Deficiencies
- Lipid Metabolism Disorders
- Tauopathies
- Cognition Disorders
- Language Disorders
- Communication Disorders
- Intracranial Arterial Diseases
- Speech Disorders
- Frontotemporal Lobar Degeneration
- Intracranial Arteriosclerosis
- Leukoencephalopathies
- Aphasia
- Obesity
- Dementia
- Dyslipidemias
- Alzheimer Disease
- Cognitive Dysfunction
- Body Weight
- Lewy Body Disease
- Frontotemporal Dementia
- Aphasia, Primary Progressive
- Pick Disease of the Brain
- Dementia, Vascular
- Obesity, Abdominal
Other Study ID Numbers
- THMA 2021-21
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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