An empirical Q-Matrix validation method for the polytomous G-DINA model

Journal article


de la Torre, Jimmy, Qiu, Xue-Lan and Santos, Kevin Carl. (2022). An empirical Q-Matrix validation method for the polytomous G-DINA model. Psychometrika. 87(2), pp. 693-724. https://doi.org/10.1007/s11336-021-09821-x
Authorsde la Torre, Jimmy, Qiu, Xue-Lan and Santos, Kevin Carl
Abstract

A number of empirically based Q-matrix validation methods are available in the literature, all of which were developed for cognitive diagnosis models (CDMs) involving dichotomous attributes. However, in many applications, it is more instructionally relevant to classify students into more than two categories (e.g., no mastery, basic mastery, and advanced mastery). To extend the practical utility of CDMs, methods for validating the Q-matrix for CDMs that measure polytomous attributes are needed. This study focuses on validating the Q-matrix of the generalized deterministic input, noisy, “and” gate model for polytomous attributes (pG-DINA). The pGDI, an extension of the G-DINA model discrimination index, is proposed for polytomous attributes. The pGDI serves as the basis of a validation method that can be used not only to identify potential misspecified q-entries, but also to suggest more appropriate attribute-level specifications. The theoretical properties of the pGDI are underpinned by several mathematical proofs, whereas its practical viability is examined using simulation studies covering various conditions. The results show that the method can accurately identify misspecified q-entries and suggest the correct attribute-level specifications, particularly when high-quality items are involved. The pGDI is applied to a proportional reasoning test that measures several polytomous attributes.

Keywordscognitive diagnosis models; G-DINA; Q-matrix validation; polytomous attributes
Year2022
JournalPsychometrika
Journal citation87 (2), pp. 693-724
PublisherSpringer
ISSN0033-3123
Digital Object Identifier (DOI)https://doi.org/10.1007/s11336-021-09821-x
PubMed ID34843060
Scopus EID2-s2.0-85120054252
Page range693-724
FunderHong Kong Research Grant Council (HKRGC)
Publisher's version
License
All rights reserved
File Access Level
Controlled
Output statusPublished
Publication dates
Online29 Nov 2021
Publication process dates
Deposited17 Nov 2023
Grant ID17602818
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