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Adaptação cultural e propriedades psicométricas iniciais do instrumento DISABKIDS ® - Cystic Fibrosis Module - versão brasileira

Standard

Adaptação cultural e propriedades psicométricas iniciais do instrumento DISABKIDS ® - Cystic Fibrosis Module - versão brasileira. / Serio dos Santos, Danielle Maria de Souza; Deon, Keila Cristiane; Fegadolli, Claudia; Reis, Roberta Alvarenga; Torres, Lidia Alice Gomes Monteiro Marin; Bullinger-Naber, Monika; Benedita dos Santos, Claudia.

In: REV ESC ENFERM USP, Vol. 47, No. 6, 01.12.2013, p. 1311-7.

Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

Harvard

Serio dos Santos, DMDS, Deon, KC, Fegadolli, C, Reis, RA, Torres, LAGMM, Bullinger-Naber, M & Benedita dos Santos, C 2013, 'Adaptação cultural e propriedades psicométricas iniciais do instrumento DISABKIDS ® - Cystic Fibrosis Module - versão brasileira', REV ESC ENFERM USP, vol. 47, no. 6, pp. 1311-7. https://doi.org/10.1590/S0080-623420130000600009

APA

Serio dos Santos, D. M. D. S., Deon, K. C., Fegadolli, C., Reis, R. A., Torres, L. A. G. M. M., Bullinger-Naber, M., & Benedita dos Santos, C. (2013). Adaptação cultural e propriedades psicométricas iniciais do instrumento DISABKIDS ® - Cystic Fibrosis Module - versão brasileira. REV ESC ENFERM USP, 47(6), 1311-7. https://doi.org/10.1590/S0080-623420130000600009

Vancouver

Serio dos Santos DMDS, Deon KC, Fegadolli C, Reis RA, Torres LAGMM, Bullinger-Naber M et al. Adaptação cultural e propriedades psicométricas iniciais do instrumento DISABKIDS ® - Cystic Fibrosis Module - versão brasileira. REV ESC ENFERM USP. 2013 Dec 1;47(6):1311-7. https://doi.org/10.1590/S0080-623420130000600009

Bibtex

@article{787729e8b9a2442d87a2ff4979992d40,
title = "Adapta{\c c}{\~a}o cultural e propriedades psicom{\'e}tricas iniciais do instrumento DISABKIDS {\textregistered} - Cystic Fibrosis Module - vers{\~a}o brasileira",
abstract = "This study aimed to perform the cultural adaptation and describe the initial psychometric properties of the DISABKIDS{\textregistered}-Cystic Fibrosis Module instrument to measure health-related quality of life for children and adolescents and their parents/caregivers. Methodological study of sequential development, including 126 participants in four Brazilian states. Involved translation and back translation of items, semantic and conceptual equivalence, face validity and description of the initial psychometric properties related to the construct and reliability. For semantic equivalence of the adapted version, there were adjustments in the phrasing of an item. The instrument showed satisfactory internal consistency with Cronbach's alpha values between 0.70 and 0.85, convergent validity with correlation values above 0.40 in 85% of the items and divergent validity with scale fit higher than 75%. The Brazilian version of DISABKIDS{\textregistered} - CFM will certainly constitute a valid and reliable instrument for measuring the quality of life of Brazilian children and adolescents with cystic fibrosis.",
author = "{Serio dos Santos}, {Danielle Maria de Souza} and Deon, {Keila Cristiane} and Claudia Fegadolli and Reis, {Roberta Alvarenga} and Torres, {Lidia Alice Gomes Monteiro Marin} and Monika Bullinger-Naber and {Benedita dos Santos}, Claudia",
year = "2013",
month = dec,
day = "1",
doi = "10.1590/S0080-623420130000600009",
language = "Portugiesisch",
volume = "47",
pages = "1311--7",
journal = "REV ESC ENFERM USP",
issn = "0080-6234",
publisher = "UNIV SAO PAOLO",
number = "6",

}

RIS

TY - JOUR

T1 - Adaptação cultural e propriedades psicométricas iniciais do instrumento DISABKIDS ® - Cystic Fibrosis Module - versão brasileira

AU - Serio dos Santos, Danielle Maria de Souza

AU - Deon, Keila Cristiane

AU - Fegadolli, Claudia

AU - Reis, Roberta Alvarenga

AU - Torres, Lidia Alice Gomes Monteiro Marin

AU - Bullinger-Naber, Monika

AU - Benedita dos Santos, Claudia

PY - 2013/12/1

Y1 - 2013/12/1

N2 - This study aimed to perform the cultural adaptation and describe the initial psychometric properties of the DISABKIDS®-Cystic Fibrosis Module instrument to measure health-related quality of life for children and adolescents and their parents/caregivers. Methodological study of sequential development, including 126 participants in four Brazilian states. Involved translation and back translation of items, semantic and conceptual equivalence, face validity and description of the initial psychometric properties related to the construct and reliability. For semantic equivalence of the adapted version, there were adjustments in the phrasing of an item. The instrument showed satisfactory internal consistency with Cronbach's alpha values between 0.70 and 0.85, convergent validity with correlation values above 0.40 in 85% of the items and divergent validity with scale fit higher than 75%. The Brazilian version of DISABKIDS® - CFM will certainly constitute a valid and reliable instrument for measuring the quality of life of Brazilian children and adolescents with cystic fibrosis.

AB - This study aimed to perform the cultural adaptation and describe the initial psychometric properties of the DISABKIDS®-Cystic Fibrosis Module instrument to measure health-related quality of life for children and adolescents and their parents/caregivers. Methodological study of sequential development, including 126 participants in four Brazilian states. Involved translation and back translation of items, semantic and conceptual equivalence, face validity and description of the initial psychometric properties related to the construct and reliability. For semantic equivalence of the adapted version, there were adjustments in the phrasing of an item. The instrument showed satisfactory internal consistency with Cronbach's alpha values between 0.70 and 0.85, convergent validity with correlation values above 0.40 in 85% of the items and divergent validity with scale fit higher than 75%. The Brazilian version of DISABKIDS® - CFM will certainly constitute a valid and reliable instrument for measuring the quality of life of Brazilian children and adolescents with cystic fibrosis.

U2 - 10.1590/S0080-623420130000600009

DO - 10.1590/S0080-623420130000600009

M3 - SCORING: Zeitschriftenaufsatz

C2 - 24626356

VL - 47

SP - 1311

EP - 1317

JO - REV ESC ENFERM USP

JF - REV ESC ENFERM USP

SN - 0080-6234

IS - 6

ER -