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Efficacy of Caregiver Training Program in Enhancing Caregiver and Patient Outcomes

Primary Purpose

Alzheimer Disease, Dementia, Caregiver Burden

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
The MapHabit System
Sponsored by
MapHabit, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Alzheimer Disease focused on measuring Alzheimer Disease, Dementia, Caregiver Burden, Activities of Daily Living, Assistive Technology

Eligibility Criteria

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

Inclusion Criteria:

  • Individual diagnosed with Alzheimer's disease or other related dementia (ADRD) in their mild to moderate stage of impairment
  • Participating caregiver of individual with dementia must be the primary caregiver
  • Proficient in English

Exclusion Criteria:

  • Individual not diagnosed with ADRD
  • Participating caregiver of individual with dementia is NOT the primary caregiver
  • Not proficient in English

Sites / Locations

  • MapHabit, Inc.

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Caregiver Training Program

The MapHabit System

Arm Description

This condition will involve the implementation of an assistive technology software (named the MapHabit System) with an added Caregiver Training Program into the daily care of individuals with mild to moderate stages of Alzheimer's disease and related dementias. The MapHabit System (MHS) is a commercially available visual mapping software application that utilizes visual, audio, and text media to create step-by-step visual guides to assist individuals and their caregivers in structuring and accomplishing activities of daily living (ADLs). The application will be made available to families through compatible tablets.

This control condition will act as the active comparator to the experimental condition. The same assistive technology, the MapHabit System, will be given to a separate group of participants. The difference here will be that the software will be a version that does not include the caregiver training program.

Outcomes

Primary Outcome Measures

Change in User Interaction and Engagement from baseline at 6 months
18-item quality-of-life questionnaire (QoL-18) evaluates a range of participants' behaviors, including mood, engagement, and memory at the end of the study compared to before the use of the MHS. The instrument is scored on a Likert Scale, ranging from 1-10. A higher number indicates better outcome.
Change in Zarit Burden Assessment Caregiver Strain instrument from baseline at 6 months
18-item questionnaire assessing the various stresses caregivers experienced relating to caring for an individual with cognitive impairment. The total score ranges from 0-72, with a higher score reflecting higher stress and burden on the caregiver.
Change in Alzheimer's Disease Cooperative Study - Activities of Daily Living Inventory (ADCS-ADL) from baseline at 6 months
Assesses an individual with dementia's ability to carry out activities of daily living. The total score ranges from 0-53, with a higher score representing better performance in completing activities of daily living by the individual with dementia.
Change in Quality of Life - 18 (QoL-18) from baseline at 6 months
18-item quality-of-life questionnaire (QoL-18) evaluated a range of participants' behaviors, including mood, engagement, and memory at the middle and end of the study compared to before the use of the MHS. The instrument is scored on a Likert Scale, ranging from 1-10. A higher number indicates better outcome.
Change in Brief Quality of Life - 8 (QoL-8) from baseline at 6 months
8-items selected from the Wisconsin Quality of Life Caregiver Questionnaire evaluated a range of participants' behaviors, including mood, engagement, and memory at the middle and end of the study compared to before the use of the MHS. The instrument is scored on a Likert Scale, ranging from 1-10. A higher number indicates better outcome.
Change in Caregiver Self-Assessment Questionnaire from baseline at 6 months
12-item, caregiver self-report measure of stress levels

Secondary Outcome Measures

2-item Satisfaction Scale (SS-2)
Quantifies caregivers' endorsements to two survey questions: How satisfied were they with the MHS? Would they recommend MHS to others? Both questions are scored on a 10-point scale, with a higher value reflecting a better outcome/experience.
Pain and Sleep Questionnaire
5-item questionnaire developed to assess the impact of pain on quality of sleep
Generalized Anxiety Disorder (GAD7) Scale
7-item questionnaire used as an initial screening tool for generalized anxiety disorder
Anger Management Scale
12-item questionnaire designed to monitor and evaluate progress in controlling and managing anger

Full Information

First Posted
August 31, 2022
Last Updated
October 17, 2023
Sponsor
MapHabit, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT05527405
Brief Title
Efficacy of Caregiver Training Program in Enhancing Caregiver and Patient Outcomes
Official Title
Efficacy of Caregiver Training Program in Enhancing Caregiver and Patient Outcomes in Visual Mapping Assistive Technology
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
March 2024 (Anticipated)
Primary Completion Date
August 2025 (Anticipated)
Study Completion Date
August 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
MapHabit, Inc.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
As part of Phase II of the NIH SBIR grant, the study will conduct a randomized controlled clinical trial in which the MapHabit system (MHS) will offer a caregiver training product that is linked to MHS, an Alzheimer's disease or related dementias (AD/ADRD) assistive technology product that uses visual maps to improve a patient's behavior and sense of autonomy. MapHabit's combined areas of focus, i.e., offer a single integrated product to address the caregiver and the person under this caregiver's care, are unique and will create a new standard in the field to reduce caregiver burden in the setting of caring for individuals with AD/ADRD. Additionally, the study will integrate enhanced user support modules, i.e., gamifying, dashboarding, and social networking, to improve the Caregiver Training Program (CTP) experience.The study will be a randomized controlled clinical trial, in which two conditions will be investigated: 1) control condition in which the MHS alone is incorporated in the participant's daily care and 2) experimental condition in which the MHS+CTP is implemented into the daily care received by participants. The sample size will be a total of 50 patient-caregiver dyads, 25 in each condition. The study duration will be a 6-month intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer Disease, Dementia, Caregiver Burden, Assistive Technology
Keywords
Alzheimer Disease, Dementia, Caregiver Burden, Activities of Daily Living, Assistive Technology

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study will be a randomized controlled clinical trial in which two conditions will be investigated: a control and an experimental condition.
Masking
ParticipantOutcomes Assessor
Masking Description
Statistical analyses of all data will be carried out independently of investigators by a biostatistical resource department of an academic health center for validation.
Allocation
Randomized
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Caregiver Training Program
Arm Type
Experimental
Arm Description
This condition will involve the implementation of an assistive technology software (named the MapHabit System) with an added Caregiver Training Program into the daily care of individuals with mild to moderate stages of Alzheimer's disease and related dementias. The MapHabit System (MHS) is a commercially available visual mapping software application that utilizes visual, audio, and text media to create step-by-step visual guides to assist individuals and their caregivers in structuring and accomplishing activities of daily living (ADLs). The application will be made available to families through compatible tablets.
Arm Title
The MapHabit System
Arm Type
Active Comparator
Arm Description
This control condition will act as the active comparator to the experimental condition. The same assistive technology, the MapHabit System, will be given to a separate group of participants. The difference here will be that the software will be a version that does not include the caregiver training program.
Intervention Type
Device
Intervention Name(s)
The MapHabit System
Intervention Description
The MapHabit System (MHS) is a commercially available visual mapping software application that utilizes visual, audio, and text media to create step-by-step visual guides to assist individuals and their caregivers in structuring and accomplishing activities of daily living (ADLs). The goal of the application is to develop and facilitate habits and routines using structured visual and auditory stimuli that can be customized by the user and can include educational and lesson-based material in addition to ADLs. The application will be made available to families through compatible smartphones and tablets. Depending on the condition, participants will receive a specific version of the application. The experimental condition will receive the version that incorporates gamified content and structure. The MHS is a general wellness product and there is no regulatory oversight of the MapHabit System mapping functionality. This functionality is not a regulated medical device.
Primary Outcome Measure Information:
Title
Change in User Interaction and Engagement from baseline at 6 months
Description
18-item quality-of-life questionnaire (QoL-18) evaluates a range of participants' behaviors, including mood, engagement, and memory at the end of the study compared to before the use of the MHS. The instrument is scored on a Likert Scale, ranging from 1-10. A higher number indicates better outcome.
Time Frame
Pre-Post: The instrument will be administered to the participants at baseline, post-intervention (6 months), and at the 3-month follow-up..
Title
Change in Zarit Burden Assessment Caregiver Strain instrument from baseline at 6 months
Description
18-item questionnaire assessing the various stresses caregivers experienced relating to caring for an individual with cognitive impairment. The total score ranges from 0-72, with a higher score reflecting higher stress and burden on the caregiver.
Time Frame
Pre-Post: The instrument will be administered to the participants at baseline, post-intervention (6 months), and at the 3-month follow-up.
Title
Change in Alzheimer's Disease Cooperative Study - Activities of Daily Living Inventory (ADCS-ADL) from baseline at 6 months
Description
Assesses an individual with dementia's ability to carry out activities of daily living. The total score ranges from 0-53, with a higher score representing better performance in completing activities of daily living by the individual with dementia.
Time Frame
Pre-Post: The instrument will be administered to the participants at baseline, post-intervention (6 months), and at the 3-month follow-up.
Title
Change in Quality of Life - 18 (QoL-18) from baseline at 6 months
Description
18-item quality-of-life questionnaire (QoL-18) evaluated a range of participants' behaviors, including mood, engagement, and memory at the middle and end of the study compared to before the use of the MHS. The instrument is scored on a Likert Scale, ranging from 1-10. A higher number indicates better outcome.
Time Frame
Pre-Post: The instrument will be administered to the participants at baseline, post-intervention (6 months), and at the 3-month follow-up.
Title
Change in Brief Quality of Life - 8 (QoL-8) from baseline at 6 months
Description
8-items selected from the Wisconsin Quality of Life Caregiver Questionnaire evaluated a range of participants' behaviors, including mood, engagement, and memory at the middle and end of the study compared to before the use of the MHS. The instrument is scored on a Likert Scale, ranging from 1-10. A higher number indicates better outcome.
Time Frame
Pre-Post: The instrument will be administered to the participants at baseline, post-intervention (6 months), and at the 3-month follow-up.
Title
Change in Caregiver Self-Assessment Questionnaire from baseline at 6 months
Description
12-item, caregiver self-report measure of stress levels
Time Frame
Pre-Post: The instrument will be administered to the participants at baseline, post-intervention (6 months), and at the 3-month follow-up.
Secondary Outcome Measure Information:
Title
2-item Satisfaction Scale (SS-2)
Description
Quantifies caregivers' endorsements to two survey questions: How satisfied were they with the MHS? Would they recommend MHS to others? Both questions are scored on a 10-point scale, with a higher value reflecting a better outcome/experience.
Time Frame
The instrument was administered to the participants after the completion of the study duration (i.e., assessed at 6 months)
Title
Pain and Sleep Questionnaire
Description
5-item questionnaire developed to assess the impact of pain on quality of sleep
Time Frame
Pre-Post: The assessment will be administered at baseline, post-intervention (6 months), and at the 3-month follow-up.
Title
Generalized Anxiety Disorder (GAD7) Scale
Description
7-item questionnaire used as an initial screening tool for generalized anxiety disorder
Time Frame
Pre-Post: The assessment will be administered at baseline, post-intervention (6 months), and at the 3-month follow-up.
Title
Anger Management Scale
Description
12-item questionnaire designed to monitor and evaluate progress in controlling and managing anger
Time Frame
Pre-Post: The assessment will be administered at baseline, post-intervention (6 months), and at the 3-month follow-up.

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Individual diagnosed with Alzheimer's disease or other related dementia (ADRD) in their mild to moderate stage of impairment Participating caregiver of individual with dementia must be the primary caregiver Proficient in English Exclusion Criteria: Individual not diagnosed with ADRD Participating caregiver of individual with dementia is NOT the primary caregiver Not proficient in English
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Brittany Montgomery, MS
Phone
6786206171
Email
bmontgomery@maphabit.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stuart Zola
Organizational Affiliation
MapHabit, Inc.
Official's Role
Principal Investigator
Facility Information:
Facility Name
MapHabit, Inc.
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30308
Country
United States
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Matt Golden, BBA
Phone
914-330-1776
Email
mgolden@maphabit.com
First Name & Middle Initial & Last Name & Degree
Stuart Zola, PhD
First Name & Middle Initial & Last Name & Degree
Brittany Montgomery, MS

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All of the individual participant data collected during the trial, after deidentification.
IPD Sharing Time Frame
Immediately following publication. No end date.
IPD Sharing Access Criteria
Researchers who provide a methodologically sound proposal. Proposals should be directed to szola@maphabit.com. To gain access, data requestors will need to sign a data access agreement.
Citations:
PubMed Identifier
31796718
Citation
Boatman F, Golden M, Jin J, Kim Y, Law S, Lu A, Merriam N, Zola S. Assistive technology: Visual mapping combined with mobile software can enhance quality of life and ability to carry out activities of daily living in individuals with impaired memory. Technol Health Care. 2020;28(2):121-128. doi: 10.3233/THC-191980.
Results Reference
background
PubMed Identifier
34269690
Citation
Kelleher J, Zola S, Cui X, Chen S, Gerber C, Parker MW, Davis C, Law S, Golden M, Vaughan CP. Personalized Visual Mapping Assistive Technology to Improve Functional Ability in Persons With Dementia: Feasibility Cohort Study. JMIR Aging. 2021 Oct 19;4(4):e28165. doi: 10.2196/28165.
Results Reference
background
PubMed Identifier
34334439
Citation
Parker MW, Davis C, White K, Johnson D, Golden M, Zola S. Reduced care burden and improved quality of life in African American family caregivers: Positive impact of personalized assistive technology. Technol Health Care. 2022;30(2):379-387. doi: 10.3233/THC-213049.
Results Reference
background

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Efficacy of Caregiver Training Program in Enhancing Caregiver and Patient Outcomes

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