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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02969460
Other study ID # EH-003
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date November 30, 2016
Est. completion date April 18, 2018

Study information

Verified date October 2018
Source Evidation Health
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 85
Est. completion date April 18, 2018
Est. primary completion date April 18, 2018
Accepts healthy volunteers No
Gender All
Age group 60 Years to 75 Years
Eligibility 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


Related Conditions & MeSH terms


Intervention

Behavioral:
Neurotrack Virtual Cognitive Health Program


Locations

Country Name City State
United States Evidation Health San Mateo California

Sponsors (2)

Lead Sponsor Collaborator
Evidation Health Neurotrack

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary RBANS score Repeatable Battery for the Assessment of Neuropsychological Status total score week 24
Primary RBANS score Repeatable Battery for the Assessment of Neuropsychological Status total score week 52
Secondary PHQ-9 Patient-health questionnaire 9-item scale week 24
Secondary PHQ-9 Patient-health questionnaire 9-item scale week 52
Secondary GAD-7 Generalized anxiety disorder 7-item scale week 24
Secondary GAD-7 Generalized anxiety disorder 7-item scale week 52
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