The measurement properties of tests and tools used in cystic fibrosis studies: a systematic review

Charlie McLeod; Jamie Wood; Allison Tong; André Schultz; Richard Norman; Sherie Smith; Christopher C. Blyth; Steve Webb; Alan R. Smyth; Thomas L. Snelling

doi:10.1183/16000617.0354-2020

The measurement properties of tests and tools used in cystic fibrosis studies: a systematic review

Charlie McLeod, Jamie Wood, Allison Tong, André Schultz, Richard Norman, Sherie Smith, Christopher C. Blyth, Steve Webb, Alan R. Smyth, Thomas L. Snelling

Research output: Contribution to journal › Review article › peer-review

15 Citations (Scopus)

Abstract

There is no consensus on how best to measure responses to interventions among children and adults with cystic fibrosis (CF). We have systematically reviewed and summarised the characteristics and measurement properties of tests and tools that have been used to capture outcomes in studies among people with CF, including their reliability, validity and responsiveness. This review is intended to guide researchers when selecting tests or tools for measuring treatment effects in CF trials. A consensus set of these tests and tools could improve consistency in how outcomes are captured and thereby facilitate comparisons and synthesis of evidence across studies.

Original language	English
Article number	200354
Journal	European respiratory review : an official journal of the European Respiratory Society
Volume	30
Issue number	160
DOIs	https://doi.org/10.1183/16000617.0354-2020
Publication status	Published - 30 Jun 2021

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McLeod, C., Wood, J., Tong, A., Schultz, A., Norman, R., Smith, S., Blyth, C. C., Webb, S., Smyth, A. R., & Snelling, T. L. (2021). The measurement properties of tests and tools used in cystic fibrosis studies: a systematic review. European respiratory review : an official journal of the European Respiratory Society, 30(160), Article 200354. https://doi.org/10.1183/16000617.0354-2020

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abstract = "There is no consensus on how best to measure responses to interventions among children and adults with cystic fibrosis (CF). We have systematically reviewed and summarised the characteristics and measurement properties of tests and tools that have been used to capture outcomes in studies among people with CF, including their reliability, validity and responsiveness. This review is intended to guide researchers when selecting tests or tools for measuring treatment effects in CF trials. A consensus set of these tests and tools could improve consistency in how outcomes are captured and thereby facilitate comparisons and synthesis of evidence across studies.",

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McLeod, C, Wood, J, Tong, A, Schultz, A, Norman, R, Smith, S, Blyth, CC , Webb, S, Smyth, AR & Snelling, TL 2021, 'The measurement properties of tests and tools used in cystic fibrosis studies: a systematic review', European respiratory review : an official journal of the European Respiratory Society, vol. 30, no. 160, 200354. https://doi.org/10.1183/16000617.0354-2020

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AU - McLeod, Charlie

AU - Wood, Jamie

AU - Tong, Allison

AU - Schultz, André

AU - Norman, Richard

AU - Smith, Sherie

AU - Blyth, Christopher C.

AU - Webb, Steve

AU - Smyth, Alan R.

AU - Snelling, Thomas L.

PY - 2021/6/30

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N2 - There is no consensus on how best to measure responses to interventions among children and adults with cystic fibrosis (CF). We have systematically reviewed and summarised the characteristics and measurement properties of tests and tools that have been used to capture outcomes in studies among people with CF, including their reliability, validity and responsiveness. This review is intended to guide researchers when selecting tests or tools for measuring treatment effects in CF trials. A consensus set of these tests and tools could improve consistency in how outcomes are captured and thereby facilitate comparisons and synthesis of evidence across studies.

AB - There is no consensus on how best to measure responses to interventions among children and adults with cystic fibrosis (CF). We have systematically reviewed and summarised the characteristics and measurement properties of tests and tools that have been used to capture outcomes in studies among people with CF, including their reliability, validity and responsiveness. This review is intended to guide researchers when selecting tests or tools for measuring treatment effects in CF trials. A consensus set of these tests and tools could improve consistency in how outcomes are captured and thereby facilitate comparisons and synthesis of evidence across studies.

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The measurement properties of tests and tools used in cystic fibrosis studies: a systematic review

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