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Clinical Trials/NCT05004558
NCT05004558
Unknown
Not Applicable

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

Drexel University0 sites36 target enrollmentSeptember 1, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Dementia
Sponsor
Drexel University
Enrollment
36
Primary Endpoint
Resting systolic blood pressure, measured in mmHg from 0 and above with higher numbers indicating higher blood pressure
Last Updated
4 years ago

Overview

Brief Summary

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. Participants of this study will receive a baseline health-fitness assessment at the beginning of the study. Measurements of resting blood pressure, fasting blood glucose and lipids, waist and hip circumferences, height and weight, cognitive function and quality of life will be collected at the health-fitness assessment. Participants will then receive supervised remote-based resistance exercise training with Therabands, 3 days per week for 12 weeks before receiving a second 12-week health-fitness assessment in the middle of the intervention. Participants will then receive 12 additional weeks of supervised remote-based resistance exercise training with Therabands, 3 days per week for 12 weeks before receiving a third 24-week health fitness assessment at the end of the study.

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.

Registry
clinicaltrials.gov
Start Date
September 1, 2021
End Date
June 2022
Last Updated
4 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Michael Bruneau

Assistant Professor

Drexel University

Eligibility Criteria

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

Outcomes

Primary Outcomes

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

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

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

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

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

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

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

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

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

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

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

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

Secondary Outcomes

  • Cognitive Function as Measured by the Montreal Cognitive Assessment(24 weeks)
  • Quality of Life as measured by the Short-Form (36) Health Survey(24 weeks)

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