Purpose

This study will provide data for evaluating the psychometric characteristics of the tests assessing cognitive flexibility, including their (1) internal consistency, (2) feasibility and tolerability, their (3) convergent and discriminant validity of cognitive and affective constructs such as those introduced to understand mental disorders, and (4) sensitivity (and correspondence) to individual differences. For these tests to be useful in studying clinical conditions, they must show adequate reliability, validity, and sensitivity in large samples of convenience.

Condition

Eligibility

Eligible Ages
Over 18 Years
Eligible Genders
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Adults 18 years or older - English-speaking - Live in the U.S. - Have access to an internet connected computer - Users of the mTurk and Prolific survey website

Exclusion Criteria

  • NA

Study Design

Phase
Study Type
Observational
Observational Model
Case-Crossover
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Test Group involves a single testing session with surveys and tasks relevant to the experiment involving behavioral tasks and self-report questions through an online crowd-sourcing platform
  • Diagnostic Test: Computational dissociation of the causes of cognitive rigidity in depression
    involves a single testing session with surveys and tasks relevant to the experiment involving behavioral tasks and self-report questions through an online crowd-sourcing platform

Recruiting Locations

More Details

Status
Recruiting
Sponsor
University of Minnesota

Study Contact

Matthew Maple
612-946-1424
maple036@umn.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.