Use case: clinical trials
Cognitive tests for clinical trials and sponsored studies
Add scored cognitive tests to investigator-led and sponsored studies, with locked protocol versions, version records in every export and participant data stored in the United States.
ConductCognition is for research use only. Use it for exploratory and investigator-led outcomes. It is not FDA-cleared or 21 CFR Part 11 compliant, so it does not suit data collected for a regulatory submission.
Protocol and data control
Versions in every export
Quality states
Hosting and review
The application server and the study database run in Microsoft Azure East US 2. Server routes that handle consent, trial responses, scores and exports write audit events. Details for review boards and security teams are on the US clinical research page and the HIPAA-ready testing page.
Tests often used in clinical research
- Trail Making Test A
- Trail Making Test B
- Symbol Coding
- Digit Span Test
- Verbal Learning
- Short Story Recall
- Delayed Recall Module
- Recognition Memory Test
- Verbal Fluency
- Category Fluency
- Clock Drawing Task
- Stroop Color-Word Test
- Continuous Performance Test
- Stop-Signal Task
- Psychomotor Vigilance Task
- Corsi Block-Tapping Test
- Paired Associate Learning
- Spatial Working Memory
- Rapid Visual Information Processing
- Intra/Extra Dimensional Set Shift
- One-Touch Tower Planning
- Delayed Match-to-Sample
- Pattern Recognition Memory
- Spatial Recognition Memory
All tests: the test list. Norms: test norms.
Arms and visits
A study can assign each participant to a study group, such as a treatment arm, at random, by weight or balanced, with optional caps. Test order can be fixed, random or counterbalanced. Scheduled visits are not built: run each visit as its own study with the same participant IDs. The two-study comparison export joins two of them by participant and test.
Commercial licenses
- Commercial Research: $1,499 a year, 500/year participants, 3 seats.
- Commercial Team: $3,499 a year, 3,000/year participants, 10 seats.
- Enterprise / CRO: from $9,999 a year, participant volume and seats quoted.
Every plan, with three-year prices: pricing.
Questions from sponsors and investigators
Can we use ConductCognition data in a regulatory submission?
Use it for exploratory and investigator-led outcomes. It is not FDA-cleared or 21 CFR Part 11 compliant, so it does not suit data collected for a regulatory submission.
Which license does a sponsored study need?
A commercial plan. Sponsored university or hospital studies use Commercial Research pricing, and commercial plans include commercial research rights.
Where is the data hosted?
The application server and the study database run in Microsoft Azure East US 2, in the United States.
What happens if the protocol changes during the study?
Publishing a change creates a new numbered protocol revision with its own checksum. Participants already assigned keep the revision they started, and exports record the versions each session used.
Do you sign a business associate agreement?
We support HIPAA-ready workflows and review business associate agreements with hospitals, clinics and academic medical centers.
Can we randomize participants to arms or schedule visits?
Arms, yes. A study can assign each participant to a study group at random, by weight or balanced, with optional caps. Scheduled visits are not built. Run each visit as its own study with the same participant IDs, and use the two-study comparison export to join two of them.
Plan a sponsored study
Send us your protocol, sites and outcomes to discuss with a ConductScience scientist.