Actively Recruiting

Phase Not Applicable
Age: 25Years - 65Years
All Genders
NCT06130735

Impact of Intensive Computerized Cognitive Training

Led by Brigham and Women's Hospital · Updated on 2025-11-05

30

Participants Needed

1

Research Sites

126 weeks

Total Duration

On this page

Sponsors

B

Brigham and Women's Hospital

Lead Sponsor

F

Fujifilm

Collaborating Sponsor

AI-Summary

What this Trial Is About

To investigate factors that predict cognitive enhancement following engagement in an intensive Computerized Cognitive Training Protocol.

CONDITIONS

Official Title

Impact of Intensive Computerized Cognitive Training

Who Can Participate

Age: 25Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient of the Mass General Brigham Health System with primary attention and executive functioning difficulties and/or a diagnosis of mild cognitive disorder or mild neurocognitive disorder (non-amnestic profile), due to an acquired brain injury sustained at least 12 months prior
  • Ages 25 to 65 years old
  • Proficiency in English
  • Willing and able to complete all study activities for 12 months, including travel to Brigham and Women's Hospital for four in-person assessments and two sample collections
  • Access to a computer with webcam and stable internet
  • Has a reliable study informant who can complete one questionnaire about cognition and daily functioning at four time points
Not Eligible

You will not qualify if you...

  • History of alcohol or substance abuse or dependence within the past 2 years
  • High likelihood of an underlying progressive neurodegenerative disorder
  • Moderate to severe cognitive disorder with Mini-Mental Status Examination score of 21 or less
  • Patient Health Questionnaire-9 score 19 or higher unless active depression is ruled out by provider
  • Active psychotic symptoms
  • Severe sensory losses preventing study participation even with accommodations
  • Communication difficulties preventing effective participation
  • Current participation in other pharmacological or interventional research trials
  • Life expectancy less than 2 years

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Brigham and Women's Hospital

Boston, Massachusetts, United States, 02115

Actively Recruiting

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Research Team

G

George-Ryan Ghorayeb, MA

CONTACT

K

Kayla M Riera, BS

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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