Neurotrack Virtual Cognitive Health Study
- 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
- 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
- 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
Group Intervention Description Neurotrack Virtual Cognitive Health Program Neurotrack Virtual Cognitive Health Program This 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
Name Time Method RBANS score week 52 Repeatable Battery for the Assessment of Neuropsychological Status total score
- Secondary Outcome Measures
Name Time Method GAD-7 week 52 Generalized anxiety disorder 7-item scale
PHQ-9 week 52 Patient-health questionnaire 9-item scale
Trial Locations
- Locations (1)
Evidation Health
🇺🇸San Mateo, California, United States