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Remote Game-based Exercise Program for Cognitive and Motor Function Improvement

Primary Purpose

Mild Cognitive Impairment, Dementia, Cognitive Impairment

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Tele-Exergame Platform
No Tele-Exergame Platform
Sponsored by
Baylor College of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Mild Cognitive Impairment focused on measuring tele-exercise, exergame, tele-rehabilitation, Telehealth, telemedicine, virtual reality

Eligibility Criteria

50 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults with mild cognitive impairment or dementia
  • Living independently in a residential home with a caregiver/informant
  • Able to walk at least 30 feet with or without assistance

Exclusion Criteria:

  • Immobility or major mobility disorder or inability to engage safely in the proposed weight-bearing exercise program
  • Diagnosed with severe cognitive impairment (MoCA score < 20), other neurological conditions associated with cognitive impairment
  • Subjects with major hearing/visual impairment

Sites / Locations

  • Baylor College of Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Sham Comparator

Arm Label

Remote Exercise with tele-exergame

home-based exercise without technology

Arm Description

Subjects will perform exercises remotely twice a week with tele-exergaming platform.

Subjects will perform exercises at home without tele-exergaming platform twice a week.

Outcomes

Primary Outcome Measures

Change in Balance
Change in balance from baseline to 12 weeks will be measured. Balance will be assessed by measuring center of mass sway. The investigator will use a validated wearable platform (BalanSen) to measure body sway.
Change in Cognitive Function
Changes from baseline in cognitive function at 12 weeks. Cognitive performance will be assessed using Montreal Cognitive Assessment (MoCA). Scores on the MoCA range from zero to 30, with a score of 26 and higher generally considered normal.
Change in Fear of Falling
Changes in Fear of falling will be assessed by Short Falls Efficacy Scale International (FES I) questionnaire at 12 weeks and will be compared to baseline measurements. Scores range from 16 to 64, the higher the score the more concerned the subject is with falling.

Secondary Outcome Measures

Change in Physical Activity
Changes in physical activity from baseline to 12 weeks will be assessed. Physical activity will be quantified by measuring number of taken steps per day and will be measured using a validated wearable sensor named PAMSys. Monitoring of physical activity will be done during 48h baseline and 48 hour at 12 weeks.
Change in Quality of Life
Quality of life will be assessed using a validated questionnaire, called PROMIS Global-10. The PROMIS Global-10 is a 10-item patient-reported questionnaire in which the response options are presented as 5-point (as well as a single 11-point) rating scales. The results of the questions are used to calculate two summary scores: a Global Physical Health Score and a Global Mental Health score. These scores are then standardized to the general population, using the "T-Score". The average "T-Score" for the United States population is 50 points, with a standard deviation of 10 points. Higher scores indicate a healthier patient.
change in depression
Changes in depression from baseline to 12 weeks will be assessed. Depression will be quantified by the Center for Epidemiologic Studies Depression Scale (CES-D) at baseline and 12 weeks. The CES-D consists of 20 items, and each item is scored on a scale of 0 to 3, with 0 representing "Rarely or none of the time" and 3 representing "Most or all of the time." The total score for the CES-D ranges from 0 to 60, with higher scores indicating a greater severity of depressive symptoms. A score of 16 or higher is often considered as a cutoff point for identifying individuals who may be at risk for clinical depression. However, it is important to note that the CES-D is a screening tool, not a diagnostic tool, and a higher score should prompt further evaluation by a mental health professional.
Change in Gait speed
Change from baseline in Gait speed at 12 weeks. Gait speed will be measured using a validated wearable platform (LEGSys) during habitual walking speed.

Full Information

First Posted
November 5, 2021
Last Updated
September 6, 2023
Sponsor
Baylor College of Medicine
Collaborators
BioSensics
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1. Study Identification

Unique Protocol Identification Number
NCT05235113
Brief Title
Remote Game-based Exercise Program for Cognitive and Motor Function Improvement
Official Title
Tele-exergame: Remotely-supervised Exercise Platform for Improving Cognition and Motor Function Using Telemedicine
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
October 31, 2023 (Anticipated)
Primary Completion Date
September 9, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Baylor College of Medicine
Collaborators
BioSensics

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
As our population ages, more older adults face motor-cognitive declines, increasing their risk of falls and fear of falling. Exercise is an effective way to maintain cognitive function, as supported by recent studies. However, those with poor motor and cognitive abilities often struggle to visit rehabilitation centers, leading to high dropout rates and low adherence to unsupervised programs. A remote exercise program tailored for individuals with cognitive impairments is urgently needed to preserve cognitive function, promote independent living, and reduce related costs. Researchers aim to develop an in-home system for adults with mild cognitive issues or dementia, designed to improve balance and cognition while being remotely supervised through telemedicine.
Detailed Description
This study aims to develop and validate a remote exercise intervention for individuals at risk of or experiencing dementia using a wearable sensor-enabled platform, called Tele-Exergame. This approach could preserve cognitive function, promote independent living, reduce costs related to cognitive-motor decline, and advance remote technology use for screening cognitive and motor performance in older adults. The findings are crucial for healthcare providers, clinicians, seniors, and caregivers. 110 participants will be randomly assigned to either the intervention or control group, both undergoing a 12-week home exercise program for 30 minutes twice weekly. The intervention group will complete sessions remotely using Tele-exergame, while the control group will participate in home-based exercise without technology.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mild Cognitive Impairment, Dementia, Cognitive Impairment, Memory Loss
Keywords
tele-exercise, exergame, tele-rehabilitation, Telehealth, telemedicine, virtual reality

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Participants will be randomized to intervention (IG) or control group (CG) with ratio of 1:1. The entire cohort will perform leg and foot exercises twice a week. The IG will use the Tele-exergaming platform, and the CG will do the exercises without the platform.
Masking
Participant
Allocation
Randomized
Enrollment
110 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Remote Exercise with tele-exergame
Arm Type
Active Comparator
Arm Description
Subjects will perform exercises remotely twice a week with tele-exergaming platform.
Arm Title
home-based exercise without technology
Arm Type
Sham Comparator
Arm Description
Subjects will perform exercises at home without tele-exergaming platform twice a week.
Intervention Type
Device
Intervention Name(s)
Tele-Exergame Platform
Intervention Description
Subjects will perform exercises remotely twice a week with tele-exergaming platform.
Intervention Type
Device
Intervention Name(s)
No Tele-Exergame Platform
Intervention Description
Subjects will perform exercises in the home exercise twice a week without tele-exergaming platform.
Primary Outcome Measure Information:
Title
Change in Balance
Description
Change in balance from baseline to 12 weeks will be measured. Balance will be assessed by measuring center of mass sway. The investigator will use a validated wearable platform (BalanSen) to measure body sway.
Time Frame
Baseline and 12 weeks
Title
Change in Cognitive Function
Description
Changes from baseline in cognitive function at 12 weeks. Cognitive performance will be assessed using Montreal Cognitive Assessment (MoCA). Scores on the MoCA range from zero to 30, with a score of 26 and higher generally considered normal.
Time Frame
Baseline and 12 weeks
Title
Change in Fear of Falling
Description
Changes in Fear of falling will be assessed by Short Falls Efficacy Scale International (FES I) questionnaire at 12 weeks and will be compared to baseline measurements. Scores range from 16 to 64, the higher the score the more concerned the subject is with falling.
Time Frame
Baseline and 12 weeks
Secondary Outcome Measure Information:
Title
Change in Physical Activity
Description
Changes in physical activity from baseline to 12 weeks will be assessed. Physical activity will be quantified by measuring number of taken steps per day and will be measured using a validated wearable sensor named PAMSys. Monitoring of physical activity will be done during 48h baseline and 48 hour at 12 weeks.
Time Frame
Baseline and 12 weeks
Title
Change in Quality of Life
Description
Quality of life will be assessed using a validated questionnaire, called PROMIS Global-10. The PROMIS Global-10 is a 10-item patient-reported questionnaire in which the response options are presented as 5-point (as well as a single 11-point) rating scales. The results of the questions are used to calculate two summary scores: a Global Physical Health Score and a Global Mental Health score. These scores are then standardized to the general population, using the "T-Score". The average "T-Score" for the United States population is 50 points, with a standard deviation of 10 points. Higher scores indicate a healthier patient.
Time Frame
Baseline and 12 weeks
Title
change in depression
Description
Changes in depression from baseline to 12 weeks will be assessed. Depression will be quantified by the Center for Epidemiologic Studies Depression Scale (CES-D) at baseline and 12 weeks. The CES-D consists of 20 items, and each item is scored on a scale of 0 to 3, with 0 representing "Rarely or none of the time" and 3 representing "Most or all of the time." The total score for the CES-D ranges from 0 to 60, with higher scores indicating a greater severity of depressive symptoms. A score of 16 or higher is often considered as a cutoff point for identifying individuals who may be at risk for clinical depression. However, it is important to note that the CES-D is a screening tool, not a diagnostic tool, and a higher score should prompt further evaluation by a mental health professional.
Time Frame
Baseline and 12 weeks
Title
Change in Gait speed
Description
Change from baseline in Gait speed at 12 weeks. Gait speed will be measured using a validated wearable platform (LEGSys) during habitual walking speed.
Time Frame
Baseline and 12 weeks
Other Pre-specified Outcome Measures:
Title
Supportive care acceptability
Description
To evaluate the acceptability of each in-home exercise program (both the tele-exergame and the non-tele-exergame exercises), we will employ a survey based on the Technology Acceptance Model. This survey will be administered to all participants, assessing their perceptions of ease of use, usefulness, technology anxiety, and intention to use. Each response will be rated on a 5-point Likert scale, ranging from "strongly disagree" to "strongly agree". This will be subsequently translated to a 0 to 4 scale for final evaluation, with higher scores indicating greater acceptability. The assessment will take place twice: initially at baseline, after the participants have tested the tele-exergame in the clinic for training purposes, and subsequently at the 12-week mark upon completion of the in-home exercise program.
Time Frame
Baseline and 12 weeks
Title
Adherence
Description
We will assess adherence to the prescribed in-home exercise program through the use of an exercise diary and phone interview on monthly basis. In the intervention group (IG), we will also objectively quantify adherence. Adherence will be defined by the frequency and duration of in-home exercises performed over a 12-week period. We will record and review adherence data on a monthly basis for three months.
Time Frame
week 4, week 8, week 12
Title
intervention related dropout
Description
We will categorize participants as intervention-related dropouts if they miss exercises for four consecutive weeks, decide to discontinue the exercise program, or experience any exercise-related adverse events. However, if a participant drops out due to non-exercise related reasons (e.g., developing a condition that limits their ability to participate in the program, passing away, traveling, relocating), we will not consider this an intervention-related dropout. Intervention-related dropout will be calculated as a percentage of the total number of participants in each group. We will collect this data on a monthly basis.
Time Frame
week 4, week 8, week 12

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults with diagnosed with dementia or cognitive impairment Living independently in a residential home with a caregiver/informant Able to walk at least 30 feet with or without assistance Exclusion Criteria: Immobility or major mobility disorder or inability to engage safely in the proposed weight-bearing exercise program Diagnosed with severe cognitive impairment (MoCA score < 16) Subjects with major hearing/visual impairment
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Bijan Najafi, PhD
Phone
713-798-7536
Email
bijan.najafi@bcm.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Maria Noun, BS
Phone
713-798-7538
Email
maria.noun@bcm.edu
Facility Information:
Facility Name
Baylor College of Medicine
City
Houston
State/Province
Texas
ZIP/Postal Code
77498
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bijan Najafi, PhD
Phone
713-798-7536
Email
bijan.najafi@bcm.edu
First Name & Middle Initial & Last Name & Degree
Maria Noun, BS
Phone
713-798-7538

12. IPD Sharing Statement

Citations:
PubMed Identifier
36498431
Citation
Park C, Mishra RK, York MK, Enriquez A, Lindsay A, Barchard G, Vaziri A, Najafi B. Tele-Medicine Based and Self-Administered Interactive Exercise Program (Tele-Exergame) to Improve Cognition in Older Adults with Mild Cognitive Impairment or Dementia: A Feasibility, Acceptability, and Proof-of-Concept Study. Int J Environ Res Public Health. 2022 Dec 6;19(23):16361. doi: 10.3390/ijerph192316361.
Results Reference
result

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Remote Game-based Exercise Program for Cognitive and Motor Function Improvement

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