A Novel Computer-Based Functional Skills Assessment and Training Program

Sponsor
i-Function, Inc. (Industry)
Overall Status
Recruiting
CT.gov ID
NCT04679441
Collaborator
(none)
180
2
3
21.9
90
4.1

Study Details

Study Description

Brief Summary

People with cognitive impairments such as Mild Cognitive Impairment (MCI), often experience difficulty performing everyday routine activities. Further, normative age-related changes in cognition often lead to deficits on previously learned skills and impede new learning such as learning of new technology systems. This is of great concern, given population aging, the increasing number of older adults with cognitive impairments, and the continual deployment of new technologies in everyday contexts. The objectives of this SBIR Phase II study is to build on a previous Phase I SBIR project and refine and further evaluate a novel integrated computer-based functional skills assessment and training (CFSAT) program that provides training on everyday tasks critical to independent living (e.g., financial and medication management) with non-impaired older adults (NC) and adults with MCI.

Condition or Disease Intervention/Treatment Phase
  • Device: The Computerized Functional Skills Assessment and Training Program
  • Device: Brain HQ Double Decision
Phase 2

Detailed Description

The CFSAT program provides training on everyday tasks critical to independent living (e.g., financial and medication management). The program currently includes six domain simulations critical to independent living: ATM Banking/Financial Management, Online Banking, Prescription Refill via Voice Menu, Kiosk Ticket Purchase, Online Shopping (and prescription refill), and Medication Management. The simulations are in a multi-media format and include graphic representations, voice and text. In the assessment component each of the six task domains includes subtasks that graduate in difficulty (e.g., check savings account balance, transfer money between accounts). The training component is designed to: 1) be consistent with adaptive training models of learning (tailored to the individual's skills); 2) adhere to current training guidelines for older adults, 3) identify the current levels of an individual's ability on the task with Item response theory strategies; 4) use dynamic-titration feedback from immediate task performance to adjust task difficulty to optimize training potential; and 5) provide immediate feedback and graduated instruction following errors, followed by repetition of the previously failed item. Performance metrics are captured in real time and include measures of accuracy and efficiency.

The proposed research will involve two phases and will be conducted at two locations: South Florida and New York City. Inclusion of two locations will allow us to expand the diversity of our sample and the generalizability of the findings across different regions of the U.S. Phase I will focus on validation of the 3rd alternative form of the fixed difficulty assessment tasks (form C); refinement of tasks to improve the graphical representations, enhance the difficulty level of the subtasks (based on findings from Phase 1), and ensure currency of the tasks; and usability testing of the refined tasks using a user-centered design approach. Data collection for Phase 1 will involve a sample of 24 older adults (8 non-impaired older adults aged 60+ (4 per site) and 16 with MCI aged 60+ (8 per site) (4 Spanish speaking in each group) and will take place in laboratory space at i-Function and a community location in NYC. The usability testing will occur on one day and involve approximately 2 hours. In Phase 1 the investigators will also develop browser-based version of the CFSAT program so that it can be launched from web browsers such as Google Chrome or Safari. This will greatly enhance the flexibility of the program, as the investigators will be able to launch the program from a variety of settings including the home. This is also a critical step for commercialization and direct to consumer sales.

Phase 2 will involve a multi-site trial to gather continued data on the efficacy of the CFSAT training with respect to functional gains and additional data on the usability, and acceptability of the program. The investigators will also gather data on: optimal training dosage; near and far transfer of training and environmental transfer of training (actual performance in the real world on the tasks trained by the program as tracked by the EMA protocol); the maintenance of training gains over time; the need for booster training; and adherence to home-based training protocols for those with MCI and non-impaired older adults (NC). In addition, the investigators will examine if computer-based cognitive training (CT) provides a priming effect that further enhances the benefits of the CFSAT training program for those with MCI.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
180 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Healthy individuals receive skills training only MCI Participants are randomized to skills training only or skills training combined with computerized cognitive trainingHealthy individuals receive skills training only MCI Participants are randomized to skills training only or skills training combined with computerized cognitive training
Masking:
Single (Outcomes Assessor)
Masking Description:
Outcomes data wil be collected in an automated manner and will be entered directly into a database
Primary Purpose:
Treatment
Official Title:
: A Novel Computer-Based Functional Skills Assessment and Training Program
Actual Study Start Date :
Aug 1, 2021
Anticipated Primary Completion Date :
Mar 31, 2023
Anticipated Study Completion Date :
May 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Healthy individuals Skills training only

These participants will receive CFSAT training only (n = 60). They will train for 24 hours over 12 weeks.

Device: The Computerized Functional Skills Assessment and Training Program
The CFSAT program provides training on everyday tasks critical to independent living (e.g., financial and medication management). The program currently includes six domain simulations critical to independent living: ATM Banking/Financial Management, Online Banking, Prescription Refill via Voice Menu, Kiosk Ticket Purchase, Online Shopping (and prescription refill), and Medication Management.

Experimental: MCI, Skills training only

These participants will receive 24 hours of CFSAT training over 12 weeks following the same training protocol as the NC sample.

Device: The Computerized Functional Skills Assessment and Training Program
The CFSAT program provides training on everyday tasks critical to independent living (e.g., financial and medication management). The program currently includes six domain simulations critical to independent living: ATM Banking/Financial Management, Online Banking, Prescription Refill via Voice Menu, Kiosk Ticket Purchase, Online Shopping (and prescription refill), and Medication Management.

Experimental: MCI, Combined treatment

Participants assigned to this condition will initially train for 3 weeks @ 60 minutes twice per week on CT (Posit Science). Participants will train 90 minutes on Double Decision and 30 minutes on Hawkeye. They can train on Hawkeye in 15- minute increments and intersperse it within the Double Decision training. They will then train CFSAT for 9 weeks at the recommended dosage. Each task will be trained twice before advancing to the next task

Device: The Computerized Functional Skills Assessment and Training Program
The CFSAT program provides training on everyday tasks critical to independent living (e.g., financial and medication management). The program currently includes six domain simulations critical to independent living: ATM Banking/Financial Management, Online Banking, Prescription Refill via Voice Menu, Kiosk Ticket Purchase, Online Shopping (and prescription refill), and Medication Management.

Device: Brain HQ Double Decision
Cognitive speed training program

Outcome Measures

Primary Outcome Measures

  1. Time to completion on each Task of the the CFAST [Change from Baseline to end of 12 weeks of training]

    Change in time to Completion time for each module

  2. Time to completion on each Task of the the CFAST [Change from baseline to 3 months after the end of 12 weeks of training]

    Change in time to Completion time for each module

Secondary Outcome Measures

  1. Performance on the Brief Assessment of Cognition App [Compared at baseline, after 12 weeks of training and 3 months after completion of training]

    6-domain computerized cognitive assessments

  2. Performance on The Virtual Reality Functional Capacity Assessment Task [Compared at baseline, after 12 weeks of training and 3 months after completion of training]

    Computerized Functional Capacity Measure

  3. EMA measurement of real world activities [For 12 weeks of training and 3 months of followup]

    Participants will be surveyed as to their participation in several critical daily activities with EMA surveys

Eligibility Criteria

Criteria

Ages Eligible for Study:
60 Years to 100 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria MCI:
  • English or Spanish speaking

  • Able to read at the 6th grade level (WRAT)

  • Able to read a computer screen and use a keyboard or mouse

  • Has a willing and reliable informant

  • Subjective memory complaints by the participant and/or collateral informant;

  • Meets Jak Bondi criteria for the diagnosis of MCI.

Inclusion Criteria HC:
  • Score on the MOCA ≥ 26
Exclusion Criteria:
  • Sensory Limitations

  • MOCA <18

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ifunction at University of Miami Miami Florida United States 33136
2 Weill Cornell Medical Center New York New York United States 10021

Sponsors and Collaborators

  • i-Function, Inc.

Investigators

  • Principal Investigator: Philip Harvey, PhD, University of Miami/iFunction

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
i-Function, Inc.
ClinicalTrials.gov Identifier:
NCT04679441
Other Study ID Numbers:
  • iFunction Phase 2
First Posted:
Dec 22, 2020
Last Update Posted:
Aug 27, 2021
Last Verified:
Aug 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 27, 2021