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Effects of Cognitive Intervention on Cognition, Mobility and Brain Electrocortical Activity

Not Applicable
Completed
Conditions
Aging
Cognitive Impairment
Motor Coordination or Function
Cognitive Decline
Interventions
Other: Computerized cognitive training
Registration Number
NCT03860441
Lead Sponsor
Science and Research Centre Koper
Brief Summary

Within this project the investigators tested the effectiveness of 2-month of computerized cognitive training (CCT) on CogniFit online platform on 77 older adults, which were randomly divided into intervention and control group. The investigators tested close (battery of cognitive functions) and far transfer (postural and mobility control, EEG, blood samples) of the CCT. Additionally, the investigators were interested into seeing a long-lasting effect, therefore participants were brought back to the laboratory 1 year post CCT.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
77
Inclusion Criteria
  • active and healthy older adults with no major health issues
  • members of the Center for Daily Activity Koper (Slovenia)
  • had normal or corrected-to-normal vision;
  • reported no history of cardiovascular, neurological, or psychiatric conditions
Exclusion Criteria
  • younger than 60
  • smoking; regular alcohol consumption;
  • acute or chronic skeletal, neuromuscular, metabolic and cardiovascular disease condition;

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Intervention groupComputerized cognitive trainingParticipants in the intervention group received 24 sessions of computerized cognitive training, with a total time of 960 min.
Active control groupComputerized cognitive trainingParticipants in the control group attended activities separate activities, such as learning about healthy lifestyle, had cooking and other social lessons for the same amount as the intervention group performed cognitive training.
Primary Outcome Measures
NameTimeMethod
Change in gait speedup to 8 weeks

The primary outcome is change in gait speed during single- and dual-task conditions from baseline to post-intervention.

Secondary Outcome Measures
NameTimeMethod
Executive control (Trail-Making Task Forms A and B)up to 8 weeks

Secondary outcome is change in executive control, measured with TMT A and B tests

Sensorimotor integration measured with EEG/ERP methodologyup to 8 weeks

Secondary outcome is change ERP components P1, N1, P2 and P3 (amplitudes and latencies)

Brain-derived neurotrophic factor (BDNF) extracted from peripheral blood samplingup to 8 weeks

Secondary outcome is change in plasma BDNF plasma extraction evaluated in pg/mL

Trial Locations

Locations (1)

Center for Daily Activity Koper (Slovenia)

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Koper, Slovenia

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