Reporting quality of clinical trial protocols: a repeated cross-sectional study about the Adherence to SPIrit Recommendations in Switzerland, CAnada and GErmany (ASPIRE-SCAGE)

<p><strong>Objectives</strong> Comprehensive protocols are key for the planning and conduct of randomised clinical trials (RCTs). Evidence of low reporting quality of RCT protocols led to the publication of the Standard Protocol Items: Recommendations for Interventional Trials (SPI...

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Main Authors: Gryaznov, D, von Niederhäusern, B, Speich, B, Kasenda, B, Ojeda-Ruiz, E, Blümle, A, Schandelmaier, S, Mertz, D, Odutayo, A, Tomonaga, Y, Amstutz, A, Pauli-Magnus, C, Gloy, V, Lohner, S, Bischoff, K, Wollmann, K, Rehner, L, Meerpohl, JJ, Nordmann, A, Klatte, K, Ghosh, N, Taji Heravi, A, Wong, J, Chow, N, Hong, P, McCord-De Iaco, KA, Sricharoenchai, S, Busse, JW, Agarwal, A, Saccilotto, R, Schwenkglenks, M, Moffa, G, Hemkens, L, Hopewell, S, Von Elm, E, Briel, M
Format: Journal article
Language:English
Published: BMJ Publishing Group 2022
_version_ 1826309544758738944
author Gryaznov, D
von Niederhäusern, B
Speich, B
Kasenda, B
Ojeda-Ruiz, E
Blümle, A
Schandelmaier, S
Mertz, D
Odutayo, A
Tomonaga, Y
Amstutz, A
Pauli-Magnus, C
Gloy, V
Lohner, S
Bischoff, K
Wollmann, K
Rehner, L
Meerpohl, JJ
Nordmann, A
Klatte, K
Ghosh, N
Taji Heravi, A
Wong, J
Chow, N
Hong, P
McCord-De Iaco, KA
Sricharoenchai, S
Busse, JW
Agarwal, A
Saccilotto, R
Schwenkglenks, M
Moffa, G
Hemkens, L
Hopewell, S
Von Elm, E
Briel, M
author_facet Gryaznov, D
von Niederhäusern, B
Speich, B
Kasenda, B
Ojeda-Ruiz, E
Blümle, A
Schandelmaier, S
Mertz, D
Odutayo, A
Tomonaga, Y
Amstutz, A
Pauli-Magnus, C
Gloy, V
Lohner, S
Bischoff, K
Wollmann, K
Rehner, L
Meerpohl, JJ
Nordmann, A
Klatte, K
Ghosh, N
Taji Heravi, A
Wong, J
Chow, N
Hong, P
McCord-De Iaco, KA
Sricharoenchai, S
Busse, JW
Agarwal, A
Saccilotto, R
Schwenkglenks, M
Moffa, G
Hemkens, L
Hopewell, S
Von Elm, E
Briel, M
author_sort Gryaznov, D
collection OXFORD
description <p><strong>Objectives</strong> Comprehensive protocols are key for the planning and conduct of randomised clinical trials (RCTs). Evidence of low reporting quality of RCT protocols led to the publication of the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) checklist in 2013. We aimed to examine the quality of reporting of RCT protocols from three countries before and after the publication of the SPIRIT checklist.</p> <p><strong>Design</strong> Repeated cross sectional study.</p> <p><strong>Setting</strong> Swiss, German and Canadian research ethics committees (RECs).</p> <p><strong>Participants</strong> RCT protocols approved by RECs in 2012 (n=257) and 2016 (n=292).</p> <p><strong>Primary and secondary outcome measures</strong> The primary outcomes were the proportion of reported SPIRIT items per protocol and the proportion of trial protocols reporting individual SPIRIT items. We compared these outcomes in protocols approved in 2012 and 2016, and built regression models to explore factors associated with adherence to SPIRIT. For each protocol, we also extracted information on general trial characteristics and assessed whether individual SPIRIT items were reported.</p> <p><strong>Results</strong> The median proportion of reported SPIRIT items among RCT protocols showed a non-significant increase from 72% (IQR, 63%–79%) in 2012 to 77% (IQR, 68%–82%) in 2016. However, in a preplanned subgroup analysis, we detected a significant improvement in investigator-sponsored protocols: the median proportion increased from 64% (IQR, 55%–72%) in 2012 to 76% (IQR, 64%–83%) in 2016, while for industry-sponsored protocols median adherence was 77% (IQR 72%–80%) for both years. The following trial characteristics were independently associated with lower adherence to SPIRIT: single-centre trial, no support from a clinical trials unit or contract research organisation, and investigator-sponsorship.</p> <p><strong>Conclusions</strong> In 2012, industry-sponsored RCT protocols were reported more comprehensively than investigator-sponsored protocols. After publication of the SPIRIT checklist, investigator-sponsored protocols improved to the level of industry-sponsored protocols, which did not improve.</p>
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spelling oxford-uuid:056e96eb-fcd6-47a5-80b0-b5413b7dfb412023-03-28T12:53:20ZReporting quality of clinical trial protocols: a repeated cross-sectional study about the Adherence to SPIrit Recommendations in Switzerland, CAnada and GErmany (ASPIRE-SCAGE) Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:056e96eb-fcd6-47a5-80b0-b5413b7dfb41EnglishSymplectic ElementsBMJ Publishing Group2022Gryaznov, Dvon Niederhäusern, BSpeich, BKasenda, BOjeda-Ruiz, EBlümle, ASchandelmaier, SMertz, DOdutayo, ATomonaga, YAmstutz, APauli-Magnus, CGloy, VLohner, SBischoff, KWollmann, KRehner, LMeerpohl, JJNordmann, AKlatte, KGhosh, NTaji Heravi, AWong, JChow, NHong, PMcCord-De Iaco, KASricharoenchai, SBusse, JWAgarwal, ASaccilotto, RSchwenkglenks, MMoffa, GHemkens, LHopewell, SVon Elm, EBriel, M<p><strong>Objectives</strong> Comprehensive protocols are key for the planning and conduct of randomised clinical trials (RCTs). Evidence of low reporting quality of RCT protocols led to the publication of the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) checklist in 2013. We aimed to examine the quality of reporting of RCT protocols from three countries before and after the publication of the SPIRIT checklist.</p> <p><strong>Design</strong> Repeated cross sectional study.</p> <p><strong>Setting</strong> Swiss, German and Canadian research ethics committees (RECs).</p> <p><strong>Participants</strong> RCT protocols approved by RECs in 2012 (n=257) and 2016 (n=292).</p> <p><strong>Primary and secondary outcome measures</strong> The primary outcomes were the proportion of reported SPIRIT items per protocol and the proportion of trial protocols reporting individual SPIRIT items. We compared these outcomes in protocols approved in 2012 and 2016, and built regression models to explore factors associated with adherence to SPIRIT. For each protocol, we also extracted information on general trial characteristics and assessed whether individual SPIRIT items were reported.</p> <p><strong>Results</strong> The median proportion of reported SPIRIT items among RCT protocols showed a non-significant increase from 72% (IQR, 63%–79%) in 2012 to 77% (IQR, 68%–82%) in 2016. However, in a preplanned subgroup analysis, we detected a significant improvement in investigator-sponsored protocols: the median proportion increased from 64% (IQR, 55%–72%) in 2012 to 76% (IQR, 64%–83%) in 2016, while for industry-sponsored protocols median adherence was 77% (IQR 72%–80%) for both years. The following trial characteristics were independently associated with lower adherence to SPIRIT: single-centre trial, no support from a clinical trials unit or contract research organisation, and investigator-sponsorship.</p> <p><strong>Conclusions</strong> In 2012, industry-sponsored RCT protocols were reported more comprehensively than investigator-sponsored protocols. After publication of the SPIRIT checklist, investigator-sponsored protocols improved to the level of industry-sponsored protocols, which did not improve.</p>
spellingShingle Gryaznov, D
von Niederhäusern, B
Speich, B
Kasenda, B
Ojeda-Ruiz, E
Blümle, A
Schandelmaier, S
Mertz, D
Odutayo, A
Tomonaga, Y
Amstutz, A
Pauli-Magnus, C
Gloy, V
Lohner, S
Bischoff, K
Wollmann, K
Rehner, L
Meerpohl, JJ
Nordmann, A
Klatte, K
Ghosh, N
Taji Heravi, A
Wong, J
Chow, N
Hong, P
McCord-De Iaco, KA
Sricharoenchai, S
Busse, JW
Agarwal, A
Saccilotto, R
Schwenkglenks, M
Moffa, G
Hemkens, L
Hopewell, S
Von Elm, E
Briel, M
Reporting quality of clinical trial protocols: a repeated cross-sectional study about the Adherence to SPIrit Recommendations in Switzerland, CAnada and GErmany (ASPIRE-SCAGE)
title Reporting quality of clinical trial protocols: a repeated cross-sectional study about the Adherence to SPIrit Recommendations in Switzerland, CAnada and GErmany (ASPIRE-SCAGE)
title_full Reporting quality of clinical trial protocols: a repeated cross-sectional study about the Adherence to SPIrit Recommendations in Switzerland, CAnada and GErmany (ASPIRE-SCAGE)
title_fullStr Reporting quality of clinical trial protocols: a repeated cross-sectional study about the Adherence to SPIrit Recommendations in Switzerland, CAnada and GErmany (ASPIRE-SCAGE)
title_full_unstemmed Reporting quality of clinical trial protocols: a repeated cross-sectional study about the Adherence to SPIrit Recommendations in Switzerland, CAnada and GErmany (ASPIRE-SCAGE)
title_short Reporting quality of clinical trial protocols: a repeated cross-sectional study about the Adherence to SPIrit Recommendations in Switzerland, CAnada and GErmany (ASPIRE-SCAGE)
title_sort reporting quality of clinical trial protocols a repeated cross sectional study about the adherence to spirit recommendations in switzerland canada and germany aspire scage
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