COMPLETED

Serious Game-based Interventions in Patients With Mild Cognitive Impairment Outside the Clinic

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

This study will evaluate the therapeutic efficacy of Neuro-World cognitive training games (Woorisoft, S. Korea) in patients with mild cognitive impairment.

Official Title

Towards the Development of a Mobile-health Technology Designed to Encourage the Use of Serious Game-based Interventions in Patients With Mild Cognitive Impairment Outside the Clinic

Quick Facts

Study Start:2022-02-17
Study Completion:2025-03-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT04920123

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:55 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Seventeen points or greater and smaller than twenty-six points on the Montreal Cognitive Assessment (MoCA)
  2. * Fifty-five years old and above
  3. * Minimal technological literacy (i.e. ability to use a tablet independently)
  4. * Having a computer for online videoconferencing-based communication (necessary for online cognitive assessments)
  1. * Confounding neurological and psychiatric disorders
  2. * History of traumatic brain injury
  3. * Clinically known hearing or vision impairment
  4. * Severe upper-limb motor impairments that could impact the use of mobile devices
  5. * Clinical presentations suggestive of dementia with Lewy bodies, progressive supranuclear palsy, multiple system atrophy, or vascular parkinsonism
  6. * Diagnosis of dementia
  7. * Major depression
  8. * Any significant upper-limb impairment that could affect tablet use
  9. * Participation in any other therapist-supervised cognitive training

Contacts and Locations

Principal Investigator

Sunghoon I Lee, PhD
PRINCIPAL_INVESTIGATOR
University of Massachusetts, Amherst

Study Locations (Sites)

University of Massachusetts, Amherst
Amherst, Massachusetts, 01003
United States
The State University of New Jersey, Rutgers
Newark, New Jersey, 07102
United States

Collaborators and Investigators

Sponsor: University of Massachusetts, Amherst

  • Sunghoon I Lee, PhD, PRINCIPAL_INVESTIGATOR, University of Massachusetts, Amherst

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-02-17
Study Completion Date2025-03-31

Study Record Updates

Study Start Date2022-02-17
Study Completion Date2025-03-31

Terms related to this study

Additional Relevant MeSH Terms

  • Mild Cognitive Impairment