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N/A N=38 Randomized Single-blind Treatment

Using Teleneuropsychology to Optimize Cognition in Healthy Aging: the Web-based Breakfast Game

Healthy Aging

Enrolled (actual)
38
Serious AEs
0.0%
Results posted
Mar 2026
Primary outcome: Primary: Changes in the Breakfast Game Performance: Number of Tables Set Score — 1.61; 1.43 score on a scale (change)

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Web-based training strategy (Behavioral); Web-based regular training (no strategy) (Behavioral)
Age
Adult, Older Adult · 60+ yrs
Sex
All
Sponsor
Columbia University
Primary completion
Jul 2024

Outcome Measures

OutcomeResultp-value
PRIMARY
Changes in the Breakfast Game Performance: Number of Tables Set Score
1.61; 1.43
PRIMARY
Changes in the Breakfast Game Performance: Cooking Time Range of Stop Times Scores
-29.26; -14.51
PRIMARY
Change in Breakfast Game Performance: Cooking Time Discrepancy Scores
-3.85; -2.29
PRIMARY
Transfer to Complex Executive/Attention Control Measure (Proximal Outcome).
0.073; -0.010
SECONDARY
Transfer to Executive Functions Composite Z-Score (Distal Outcome)
0.636; -0.653
SECONDARY
Transfer to the General Self-efficacy Scale (Distal Outcome)
-0.87; -0.89
SECONDARY
Transfer to Beck Depression Inventory (Distal Outcome)
0.42; 0.30
SECONDARY
Transfer to Beck Anxiety Inventory (Distal Outcome)
-0.139; 0.018
SECONDARY
Transfer to Cognition-Leisure Questionnaire (Distal Outcome)
-1.02; 0.94

Summary

Executive control processes involve initiate, coordinate, synchronize, and regulate elemental cognitive functions for the conduct of goal-directed behavior. The proposed research investigates whether exposure to a web-based training protocol designed to enhance executive control processes will improve cognitive performance in cognitively healthy older adults.

Eligibility Criteria

Inclusion Criteria

  • Age 60-75
  • Willingness to adhere to training protocol
  • Adequate English proficiency

Exclusion Criteria

  • Low test scores (below 26 on the Montreal Cognitive Assessment)
  • Known history of cognitive impairment, dementia, stroke, seizure disorder, or other neuropsychiatric condition judged to impact cognitive performance.
  • Taking medications known to influence cognitive performance.
  • Sensory (e.g. visual, auditory) or physical (e.g. severe arthritic, orthopedic, neurologic) impairment incompatible with use of a standard computer workstation.
  • Enrolled in a concurrent study that could affect the outcome of this study.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05506852). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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