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Substitution Heuristic on Proportional Tasks

Substitution in Adult Proportional Reasoning

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06762366
Enrollment
442
Registered
2025-01-07
Start date
2024-12-13
Completion date
2026-03-15
Last updated
2026-06-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Proportional Reasoning, Substitution Heuristic

Keywords

proportion, hueristic

Brief summary

The goal of this clinical trial is to test whether or not adults use a substitution heuristic when reasoning about proportions. The main question it aims to answer is: Do adults use a substitution heuristic when judging non-symbolic proportions, leading them to answer an easier, yet incorrect question? Researchers will compare performance at baseline with one of two conditions in order to see if forced behavioral changes can change performance on the task. Participants will be asked to compare two images and judge which has the higher proportion of the target color. Each participant will also be assigned to one of two condition where they either receive a further incentive for correct selections or are required to use more time when making their calculations.

Interventions

BEHAVIORALAdditional Incentive

During this behavioral intervention, participants will be given additional compensation for correct answers.

BEHAVIORALResponse Delay

During this behavioral intervention, participants will not be allowed to respond with their judgements until after a certain amount of time has passed.

BEHAVIORALBaseline Performance

In this intervention, the participant completes the task as it is typically administer for a baseline performance measure. The participant can respond at will and does not receive incentive for correct responses.

Sponsors

Michelle Hurst, PhD
Lead SponsorOTHER
Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
CollaboratorNIH
Rutgers, The State University of New Jersey
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
Yes

Inclusion criteria

* Typically developing people within the target age range

Exclusion criteria

* Individuals with known developmental or cognitive disorders * Participants must speak/read sufficient English to read and complete the informed consent document

Design outcomes

Primary

MeasureTime frameDescription
Proportion Correctup to 20 minutesAccuracy will be measured for each trial and combined into an overall score (i.e., proportion of trials correct).
Reaction Timeup to 20 minutesReaction time will also be tracked (i.e., time it takes to respond), with a faster reaction time indicating ease and/or efficiency with the task.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 6, 2026