A fully remote randomized trial of digital cognitive training for cognitive control in adults
| ISRCTN | ISRCTN10069297 |
|---|---|
| DOI | https://doi.org/10.1186/ISRCTN10069297 |
| Sponsor | University of California, San Francisco |
| Funders | Neuroscape Network, Patrick J. McGovern Foundation |
- Submission date
- 11/08/2026
- Registration date
- 18/08/2026
- Last edited
- 13/08/2026
- Recruitment status
- No longer recruiting
- Overall study status
- Completed
- Condition category
- Other
Plain English summary of protocol
Background and study aims
Cognitive control refers to mental abilities that support attention, working memory, and goal-directed behavior. Individual differences in cognitive control are associated with variation in everyday functioning and cognitive performance. The aim of this study was to characterize cognitive control abilities in healthy adults and evaluate the effects of digital cognitive training interventions delivered remotely through mobile devices and computers on cognitive performance. The study also examined relationships between laboratory-based cognitive measures and real-world cognitive functioning.
Who can participate?
Healthy adults aged 18 to 65 years who were fluent in English, had access to a computer or mobile device with internet connectivity, and had normal or corrected-to-normal vision and hearing. Individuals with neurological or psychiatric disorders were excluded.
What does the study involve?
Participants completed the study entirely remotely using the Nexus online research platform. After providing consent and completing baseline assessments, participants were randomly assigned to one of four digital applications, including three cognitive training interventions and one active placebo control application. Participants completed approximately 40 minutes of training per day, 5 days per week, for 6 weeks. Before and after the intervention period, participants completed cognitive assessments and questionnaires measuring attention, working memory, cognitive control, stress, and related outcomes.
What are the possible benefits and risks of participating?
Participants contributed to research investigating cognitive control and digital cognitive training interventions. Risks were considered minimal and included possible mental fatigue, boredom, frustration during cognitive tasks, or discomfort when answering questionnaires.
Where is the study run from?
Neuroscape, Department of Neurology, University of California, San Francisco (UCSF), San Francisco, California, USA. All study procedures were conducted remotely through the Nexus online platform.
When is the study starting and how long is it expected to run for?
March 2024 to February 2025
Who is funding the study?
National Institute on Aging, National Institutes of Health (NIH)USA)
Who is the main contact?
Dr. Joaquin A. Anguera
Department of Neurology
University of California, San Francisco (UCSF)
joaquin.anguera@ucsf.edu
Contact information
Principal investigator, Public, Scientific
675 Nelson Rising Ln
San Francisco
94158
United States of America
| 0000-0002-7216-0674 | |
| Phone | +1 415 702 4322 |
| joaquin.anguera@ucsf.edu |
Study information
| Primary study design | Interventional |
|---|---|
| Allocation | Randomized controlled trial |
| Masking | Blinded (masking used) |
| Control | Active |
| Assignment | Parallel |
| Purpose | Basic science |
| Scientific title | A randomized controlled trial in adults comparing mobile-delivered cognitive training with an active placebo control application for improving cognitive control, attention, and working memory |
| Study acronym | UCSF MEC Study |
| Study objectives | The primary objective of this study is to evaluate the effects of remotely delivered digital cognitive training interventions on cognitive control abilities in healthy adults. Secondary objectives are to characterize individual differences in cognitive control, examine relationships between laboratory-based and real-world measures of cognitive functioning, and compare the effects of different digital cognitive training approaches on attention, working memory, executive function, and related cognitive outcomes. |
| Ethics approval(s) |
Approved 20/02/2022, University of California San Francisco Institutional Review Board (675 Nelson Rising Ln, San Francisco, 94158, United States of America; +1 (415) 476-1814; IRB@ucsf.edu), ref: 22-36343 |
| Health condition(s) or problem(s) studied | Healthy adults |
| Intervention | Participants are randomly assigned to one of four digital intervention arms delivered remotely through the Nexus research platform (we used a block randomization approach using an online tool, with block size of 4): -Meditrain: a mindfulness-based digital cognitive training application designed to engage attention and self-regulation processes -Engage: an adaptive attention training application incorporating game-like elements designed to engage cognitive control processes -Coherence: an adaptive rhythm-based training application designed to engage attention, synchronization, and working memory processes -Worder (active placebo control): a word-search game designed to maintain participant engagement without specifically targeting cognitive control mechanisms Participants complete approximately 40 minutes of training per day, 5 days per week, for 6 weeks. Cognitive assessments and questionnaires are administered remotely before and after the intervention period to evaluate attention, working memory, cognitive control, stress, and related outcomes. Participants are allocated to intervention arms through random assignment using the Nexus platform. |
| Intervention type | Behavioural |
| Primary outcome measure(s) |
|
| Key secondary outcome measure(s) |
|
| Completion date | 02/02/2025 |
Eligibility
| Participant type(s) | |
|---|---|
| Age group | Mixed |
| Lower age limit | 18 Years |
| Upper age limit | 65 Years |
| Sex | All |
| Target sample size at registration | 800 |
| Total final enrolment | 156 |
| Key inclusion criteria | 1. Adults aged 18–65 years 2. Access to a computer or mobile device with internet connectivity 3. Fluent in English 4. Normal or corrected-to-normal vision and hearing 5. Able to provide informed consent 6. Willing to participate in a fully remote digital cognitive training study |
| Key exclusion criteria | 1. Under 18 years of age 2. Self-reported neurological disorder 3. Self-reported psychiatric disorder 4. Inability to complete study procedures remotely 5. Inability to provide informed consent |
| Date of first enrolment | 01/03/2024 |
| Date of final enrolment | 01/01/2025 |
Locations
Countries of recruitment
- United States of America
Study participating centres
Results and Publications
| Individual participant data (IPD) Intention to share | No |
|---|
Editorial Notes
13/08/2026: Trial's existence confirmed by University of California San Francisco Institutional Review Board.