NDOPSYCHO
Template benchmark

Browser experiment template fields: July 2026

This benchmark documents the current output fields and default settings for eight public DOPSYCHO templates. The CSV supports tool comparison, teaching review, and implementation checks.

Coverage

Eight template definitions were inspected at version 1.0.0.

  • Stroop color-word task: 6 documented fields, 60 default trials, 2 block(s), keyboard responses.
  • Go / No-Go inhibition task: 6 documented fields, 80 default trials, 2 block(s), keyboard responses.
  • Flanker interference task: 6 documented fields, 60 default trials, 2 block(s), keyboard responses.
  • N-back working-memory task: 6 documented fields, 72 default trials, 3 block(s), keyboard responses.
  • Posner spatial-cueing task: 6 documented fields, 72 default trials, 3 block(s), keyboard responses.
  • Corsi block-span task: 5 documented fields, 24 default trials, 2 block(s), sequence responses.
  • Delay-discounting choice task: 5 documented fields, 27 default trials, 1 block(s), choice responses.
  • Randomized vignette survey: 6 documented fields, 12 default trials, 1 block(s), scale responses.

How to use the file

Use the CSV to compare field names before configuring exports or a teaching exercise. The runnable preview shows task behavior, while the advanced editor supports protocol changes.

Limits

The table documents software defaults on the publication date. It does not establish psychometric validity, timing equivalence across devices, normative scores, or fitness for a specific study.

Version rule

Future changes to fields or defaults should publish a new dated file and retain this version for reproducibility.

Sources and scope

FAQ

Which templates are included?

The July 2026 file covers Stroop, Go/No-Go, Flanker, N-back, Posner, Corsi, delay discounting, and randomized vignette templates.

Does the file contain participant data?

No. It contains template definitions and output-field names only.

Can these defaults replace a research protocol?

No. Researchers should set trial counts, timing, exclusions, counterbalancing, and scoring from their protocol and validate the deployed study.

Updated