Using Neuroscience to Optimize Digital Health Interventions Across Adulthood
1 other identifier
interventional
44
1 country
1
Brief Summary
The goal of this study is to investigate the extent to which brain imaging data predict health behavior change, compared to participant self-reports.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable healthy
Started Jan 2019
Typical duration for not_applicable healthy
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
November 13, 2018
CompletedFirst Posted
Study publicly available on registry
November 16, 2018
CompletedStudy Start
First participant enrolled
January 17, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 18, 2020
CompletedStudy Completion
Last participant's last visit for all outcomes
May 18, 2020
CompletedFebruary 16, 2021
February 1, 2021
1.3 years
November 13, 2018
February 15, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
Change in Physical Activity as measures by FitBit
Baseline (14 days after the 1st visit), End of study (80 days after the MR visit)
Study Arms (1)
Adult Participants
EXPERIMENTALMessages regarding physical activity will be texted to participants.
Interventions
Messages regarding physical activity will be texted to participants.
Eligibility Criteria
You may qualify if:
- Healthy adults ages 30-80 who read/understand English, 50% male and 50% female, and a maximum of 50% will be white.
You may not qualify if:
- Pregnancy
- History of head injury
- Mental illness diagnosis
- Psychoactive medication
- Psychiatric or neurological history
- Claustrophobia
- Ferrous metal implanted within the body (those with fMRI-compatible implanted devices will not be excluded, but the eligibility of their devices will be first verified.)
- Asthma, injuries, or other health conditions which inhibit daily physical activity
- Subjects must not already meet the recommended amount of physical activity of moderate-intensity physical activity for 150 minutes a week or 75 minutes at vigorous-intensity a week.
- Duke students are excluded from this study
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Duke Universitylead
- Duke University: Bass Connectionscollaborator
- National Institutes of Health (NIH)collaborator
Study Sites (1)
Duke University
Durham, North Carolina, 27708, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Gregory Samanez-Larkin, PhD
Duke University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 13, 2018
First Posted
November 16, 2018
Study Start
January 17, 2019
Primary Completion
May 18, 2020
Study Completion
May 18, 2020
Last Updated
February 16, 2021
Record last verified: 2021-02
Data Sharing
- IPD Sharing
- Will not share