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Neurotrack Virtual Cognitive Health Study

Not Applicable
Completed
Conditions
Subjective Cognitive Decline
Interventions
Behavioral: Neurotrack Virtual Cognitive Health Program
Registration Number
NCT02969460
Lead Sponsor
Evidation Health
Brief Summary

The Neurotrack Virtual Cognitive Health Study is a 12-month long, prospective study that aims to evaluate the impact of the Neurotrack Virtual Cognitive Health Coaching Program on cognitive ability, anxiety and depression, and lifestyle behaviors for individuals who show signs of subjective cognitive decline.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
85
Inclusion Criteria
  • Ages 60-75
  • Individuals who show signs of subjective cognitive decline (assessed by scoring ≥ 1 on the Subjective Cognitive Decline [Short Form] Questionnaire and endorsing the Personal Worry Item on the questionnaire)
  • Have the ability to make and receive phone calls
  • Have the ability to send and receive text messages
  • Access to a desktop computer, video-teleconferencing and reliable internet connection
  • Motivated to use a daily coaching program
Exclusion Criteria
  • Significant history of mental illness, substance abuse, learning disability, or neurologic conditions
  • History of dementia
  • Ophthalmologic/visual problems that prevent individual from viewing a computer screen at a normal distance (e.g., legal blindness, detached retinas, occlusive cataracts)
  • Currently participating in a formal cognitive-training coaching program
  • Currently pregnant

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Neurotrack Virtual Cognitive Health ProgramNeurotrack Virtual Cognitive Health ProgramThis program is a multi-domain lifestyle intervention designed to prevent or delay cognitive decline and impairment in older at-risk adults. The first 6 months of the program emphasizes lifestyle change, while the last 6 months of the program emphasizes habit reinforcement. The program focuses on nutrition, physical exercise, and cognitive training.
Primary Outcome Measures
NameTimeMethod
RBANS scoreweek 52

Repeatable Battery for the Assessment of Neuropsychological Status total score

Secondary Outcome Measures
NameTimeMethod
GAD-7week 52

Generalized anxiety disorder 7-item scale

PHQ-9week 52

Patient-health questionnaire 9-item scale

Trial Locations

Locations (1)

Evidation Health

🇺🇸

San Mateo, California, United States

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