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Tailored Screening for Late-Life Depression: A Short Version of the Teate Depression Inventory (TDI-E)
A number of assessment instruments have been developed as efficacy measures of geriatric depression in clinical trials but most showed several weaknesses, such as time-consuming administration, development and validation in younger populations, and lack of discrimination between anxiety and depressi...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906150/ https://www.ncbi.nlm.nih.gov/pubmed/31866900 http://dx.doi.org/10.3389/fpsyg.2019.02693 |
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author | Balsamo, Michela Saggino, Aristide Carlucci, Leonardo |
author_facet | Balsamo, Michela Saggino, Aristide Carlucci, Leonardo |
author_sort | Balsamo, Michela |
collection | PubMed |
description | A number of assessment instruments have been developed as efficacy measures of geriatric depression in clinical trials but most showed several weaknesses, such as time-consuming administration, development and validation in younger populations, and lack of discrimination between anxiety and depression. Among the extant self-report measures of depression, the 21-item Teate Depression Inventory (TDI; Balsamo and Saggino, 2013), developed via Rasch analysis, showed a satisfactory level of diagnostic accuracy, and allowed the reduction of false positives in test scoring in adult population. The present study explored the potential improvement in the psychometric performance of the TDI in the elderly by item refinement through Rasch analysis in a sample of 836 elderly people (49.5% males; mean age = 73.28; SD = 6.56). A resulting shorter version was composed of the best-fitting and discriminative nine items from the full form. The Teate Depression Inventory (TDI-E) (E for elderly) presented good internal construct validity, with unidimensional structure, local dependency, good reliability (person separation index and Cronbach’s alpha), and no signs of differential item functioning or measurement bias due to gender and age (65 vs. 75+ years). Cut-off points and normative data provided could enhance the clinical usefulness of the TDI-E, which seems to be a promising valid and reliable tool for the screening of geriatric depression, with less risk of finding false positives due to overlapping of depression in elderly with other comorbid conditions. |
format | Online Article Text |
id | pubmed-6906150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69061502019-12-20 Tailored Screening for Late-Life Depression: A Short Version of the Teate Depression Inventory (TDI-E) Balsamo, Michela Saggino, Aristide Carlucci, Leonardo Front Psychol Psychology A number of assessment instruments have been developed as efficacy measures of geriatric depression in clinical trials but most showed several weaknesses, such as time-consuming administration, development and validation in younger populations, and lack of discrimination between anxiety and depression. Among the extant self-report measures of depression, the 21-item Teate Depression Inventory (TDI; Balsamo and Saggino, 2013), developed via Rasch analysis, showed a satisfactory level of diagnostic accuracy, and allowed the reduction of false positives in test scoring in adult population. The present study explored the potential improvement in the psychometric performance of the TDI in the elderly by item refinement through Rasch analysis in a sample of 836 elderly people (49.5% males; mean age = 73.28; SD = 6.56). A resulting shorter version was composed of the best-fitting and discriminative nine items from the full form. The Teate Depression Inventory (TDI-E) (E for elderly) presented good internal construct validity, with unidimensional structure, local dependency, good reliability (person separation index and Cronbach’s alpha), and no signs of differential item functioning or measurement bias due to gender and age (65 vs. 75+ years). Cut-off points and normative data provided could enhance the clinical usefulness of the TDI-E, which seems to be a promising valid and reliable tool for the screening of geriatric depression, with less risk of finding false positives due to overlapping of depression in elderly with other comorbid conditions. Frontiers Media S.A. 2019-12-05 /pmc/articles/PMC6906150/ /pubmed/31866900 http://dx.doi.org/10.3389/fpsyg.2019.02693 Text en Copyright © 2019 Balsamo, Saggino and Carlucci. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Psychology Balsamo, Michela Saggino, Aristide Carlucci, Leonardo Tailored Screening for Late-Life Depression: A Short Version of the Teate Depression Inventory (TDI-E) |
title | Tailored Screening for Late-Life Depression: A Short Version of the Teate Depression Inventory (TDI-E) |
title_full | Tailored Screening for Late-Life Depression: A Short Version of the Teate Depression Inventory (TDI-E) |
title_fullStr | Tailored Screening for Late-Life Depression: A Short Version of the Teate Depression Inventory (TDI-E) |
title_full_unstemmed | Tailored Screening for Late-Life Depression: A Short Version of the Teate Depression Inventory (TDI-E) |
title_short | Tailored Screening for Late-Life Depression: A Short Version of the Teate Depression Inventory (TDI-E) |
title_sort | tailored screening for late-life depression: a short version of the teate depression inventory (tdi-e) |
topic | Psychology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6906150/ https://www.ncbi.nlm.nih.gov/pubmed/31866900 http://dx.doi.org/10.3389/fpsyg.2019.02693 |
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