Cognitive Engagement and Aging Mind

Sponsor
The University of Texas at Dallas (Other)
Overall Status
Completed
CT.gov ID
NCT05924490
Collaborator
(none)
58
1
2
68
0.9

Study Details

Study Description

Brief Summary

The purpose of this research is to examine whether and to what extent training of different types of cognitive engagement will improve performance on fluid cognitive abilities that typically decline with age. The research covered by this protocol will use behavioral data that yield response latencies and accuracies of the untrained tasks, and brain activations in fMRI tasks, to test specific hypotheses about neural plasticity and cognitive plasticity from these engagement techniques. Hence, human subjects will be employed in an experiment lasting for 20 hours spanning over 2 months where they will either receive real-time strategy-based videogame training or crystallized intelligence training. In addition, long-term retention data will be obtained after 6 month post-training to investigate any long-term benefits.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Real-time strategy-based videogame training
  • Behavioral: Semantic Knowledge training
N/A

Detailed Description

The purpose of this research is to examine whether and to what extent training of different types of cognitive engagement will improve performance on fluid cognitive abilities that typically decline with age (such as, speed of information processing, working memory capacity, episodic memory, and executive functions). The research covered by this protocol will use behavioral data that yield response latencies and accuracies of the untrained tasks, and brain activations in fMRI tasks, to test specific hypotheses about the extent of transfer, if any, and the underlying cognitive constructs that may be trained in the process. Hence, human subjects will be employed in an experiment lasting for 20 hours spanning over 2 months where they will either receive real-time strategy-based videogame training or crystallized intelligence training. In addition, long-term retention data will be obtained after 6 month post-training to investigate any long-term benefits.

Study Design

Study Type:
Interventional
Actual Enrollment :
58 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Participant)
Primary Purpose:
Treatment
Official Title:
Cognitive Engagement and Aging Mind: A Randomized Control Trial to Determine the Effects of Adaptive Real-time Strategy Game Training on Cognition and Brain Functions of Older Adults
Actual Study Start Date :
Jan 31, 2013
Actual Primary Completion Date :
Apr 1, 2018
Actual Study Completion Date :
Oct 1, 2018

Arms and Interventions

Arm Intervention/Treatment
Experimental: Real-time strategy-based videogame training

Participants played a real-time strategy-based videogame in laboratory setting, Rise of Nations, for 2 hours a day, two days per week, for 5 weeks.

Behavioral: Real-time strategy-based videogame training
Rise of Nation is a complex strategy-based video game, in which individualized-adaptive feedbacks are constantly given to players based on their performance.

Active Comparator: Crystallized intelligence training

Participants completed a series of crossword puzzles each week, for 5-6 weeks. Training sessions were completed at the participants' home or area of preference. Participant received a periodic phone call (2 times per week) from research staff to update any notes or details regarding participants' study progress.

Behavioral: Semantic Knowledge training
Packages of various cross-word puzzles include word search, word ladder, and word wheel.

Outcome Measures

Primary Outcome Measures

  1. Immediate change in the composite score of executive functions [9-11 weeks]

    Change in the composite score of executive functions, and its subcomponents, from baseline to post-training. Higher change in score represents better outcome.

  2. Immediate change in the composite score of episodic memory [9-11 weeks]

    Change in the composite score of episodic memory from baseline to post-training.Higher change in score represents better outcome.

  3. Immediate change in brain activations during executive functions: multi-tasking [9-11 weeks]

    Change in fMRI brain activations from baseline to post-training.

  4. Immediate change in brain activations during executive functions: working memory updating [9-11 weeks]

    Change in fMRI brain activations from baseline to post-training.

Secondary Outcome Measures

  1. Immediate change in the composite score of working memory capacity [9-11 weeks]

    Change in the composite score of working memory capacity from baseline to post-training.Higher change in score represents better outcome.

  2. Immediate change in the fluid reasoning measure [9-11 weeks]

    Change in the fluid reasoning measure (Raven's Advanced Progressive Matrices, a paper and pencil test) from baseline to post-training. Higher change in score represents better outcome.

  3. immediate change in the composite score of cognition [9-11 weeks]

    Change in composite score of cognition from baseline to long-term retention. Composite score for overall cognition is summed across composite scores for executive function, processing speed, processing speed, working memory capacity and fluid reasoning. Higher change in score represents better outcome.

Other Outcome Measures

  1. Immediate change in the processing speed construct [9-11 weeks]

    Change in the processing speed construct from baseline to post-training. Higher change in score represents better outcome.

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Right-handed

  • over 50 Years of Age

  • native or fluent English speaker

  • not Color-blind

  • Magnetic Resonance Imaging eligible

  • Mini Mental Status Examination Score >24

Exclusion Criteria:
  • Left-handed or ambidextrous

  • younger than 50

  • cannot distinguish colors during color blindness test

  • claustrophobia

  • metal artifact in body

  • over 300 lb

  • pacemaker

  • MMSE score lower than 24

  • history of stroke

  • history of substance or alcohol abuse

  • currently taking anti-psychotic or anti-depression medication

Contacts and Locations

Locations

Site City State Country Postal Code
1 The Center for Vital Longevity (UT Dallas) Dallas Texas United States 75235

Sponsors and Collaborators

  • The University of Texas at Dallas

Investigators

  • Principal Investigator: Chandramallika Basak, Ph.D., The University of Texas at Dallas

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
The University of Texas at Dallas
ClinicalTrials.gov Identifier:
NCT05924490
Other Study ID Numbers:
  • IRB 12-57
First Posted:
Jun 29, 2023
Last Update Posted:
Jun 29, 2023
Last Verified:
May 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:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 29, 2023