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Modifying Cognitive Strategies for Comparing Proportions

M

Michelle Hurst, PhD

Status

Invitation-only

Conditions

Proportional Reasoning

Treatments

Behavioral: Verbal Interference Task

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT06635577
Pro2023001794
R00HD104990 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The goal of this study is to understand the cognitive processes underlying quantitative and relational reasoning, including the understanding of mathematical information (e.g., numbers, proportions, percentages, geometry) and related relational concepts (e.g., analogies, the concepts same/different), as well as how people's reasoning can be changed by external factors. The main question it aims to answer is:

How does the introduction of a secondary task affect the behavior of children and adults when reasoning about proportions in different formats? Participants will be asked to make judgements about images with and without the presence of a distractor task.

Enrollment

300 estimated patients

Sex

All

Ages

7 to 64 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Typically developing people within the target age range (either 8-years-old OR 18- to 64-years-old) for the study version

Exclusion criteria

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

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

300 participants in 1 patient group

Proportion Judgements
Experimental group
Description:
This is the sole arm of the study. All participants will be observed under normal conditions and then those same participants will undergo a behavioral intervention.
Treatment:
Behavioral: Verbal Interference Task

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Michelle A.R. Hurst

Data sourced from clinicaltrials.gov

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