This systematic review has been registered with the International Prospective Register of Systematic Reviews (PROSPERO, https://www.crd.york.ac.uk/prospero/, registration number: CRD42022306580). The review protocol is being conducted and reported using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocol (PRISMA-P) checklist (38), which is available as supplementary file 1.
The review is an element of the research project Improving Organized Colorectal Cancer Screening: An Implementation science study (OCCSI). Funded by swiss cancer research, and based on a mixed-methods design, OCCSI aims to build an understanding of current practices in implementing organized CRC screening programs in Switzerland. Enforced by a decentralized political structure, Swiss organized CRC screening programs are established at a cantonal level. Since the development of the first Swiss organized CRC screening program in 2013, about half of all 26 Swiss cantons have followed1. The majority of these programs were established in the years since 2019 and are at early stages of their implementation. This review will contribute to building the knowledge base on how to optimize this implementation and that of further programs to be established in Switzerland in the future.
The review is designed as a systematic integrative review (SIR), building on the SIR framework by Whittemore and Knafl (39), allowing for the inclusion of quantitative as well as qualitative study designs.
Criteria for considering studies for this review
Criteria for selecting studies for this review were developed based on the SPIDER tool (40) and include: sample, phenomenon of interest, design, evaluation, and research type.
Sample
Studies focused on adult populations who are involved in the implementation of organized colorectal cancer screening programs developed for individuals at average risk for colorectal cancer – as participants, health care professionals, administrators/ coordinators, leaders, policy developers, politicians, funders or in other roles – will be included in this systematic review. “Implementation” refers to any activities undertaken to establish, improve, or sustain an organized CRC screening program.
Phenomenon of interest
The characteristics of organized CRC screening programs developed by the International Agency for Research on Cancer (41) will be applied. These include for screening to be organized at a national or regional level, and to be based on an explicit policy. They also imply for a central team to be responsible for organizing the program, the systematic participant invitation based on prespecified target populations, and the health care services provided within the program. The existence of a structure for program quality assurance is a further characteristic.
Design
Published primary studies, i.e., studies reporting original, new data, of any research design will be eligible for this review.
Evaluation
Information about (a) determinants, i.e., factors perceived or empirically reported to influence the implementation of organized CRC screening programs and (b) the strategies used to navigate these determinants are the central findings of interest for this review. Implementation strategies will be defined as the methods or techniques used to enhance the adoption, implementation, or sustainment of organized CRC screening programs (27).
Determinants may influence program implementation in positive or negative direction and affect, e.g., program reach, engagement of health care professionals, program implementation speed, funding availability or security, and other implementation characteristics and outcomes. In identifying strategies, any activities aimed at navigating, removing, or utilizing these determinants will be included. Information about determinants and strategies may be reported as perceptions, characteristics, views, experiences or in other either qualitative or quantitative formats.
Research type
This review will include qualitative, quantitative, and mixed methods peer-reviewed primary studies. Grey literature will be limited to third sector and government evaluation reports.
Information sources and search strategy
The following databases will be searched for studies published from January 2000 onward
- CINAHL
- Cochrane
- EMBASE
- International Clinical Trials Registry Platform (ICTRP)
- MEDLINE
- PsycINFO
- Scopus
Search strategies to be used are outlined in supplementary file 2.
Supplementary searches
Websites of (non-)government health care organizations known to be engaged in promoting and scaling cancer screening efforts around the world will be screened for unpublished evaluation reports. The final list of websites will include but not be limited to:
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American Association for Cancer Research (AACR)
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Cancer Research UK
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European Cancer Organization
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European Cancer Patient Coalition
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International Agency for Research on Cancer (IARC)
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Innovative Partnership for Action Against Cancer (iPAAC)
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National Cancer Institute (U.S.)
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World Endoscopy Organization (WEO)
Websites of organizations affiliated with authors of included studies will also be searched for eligible publications. Furthermore, reference lists of previous systematic reviews identified through the search process together with reference lists of included studies will be screened for relevant literature. Finally, existing organized CRC screening programs (41) will be contacted with a request to share program-specific grey literature.
Language of publication
Studies written in Danish, English, French, German, Italian, Norwegian, Spanish, or Swedish will be included.
Data collection and management
Following the upload of all references to the online systematic review application Covidence2, all screening work will occur on this platform. A PRISMA flowchart will be developed to summarize the inputs and results of each stage of the screening process.
Study selection
Two researchers will independently screen each publication in two rounds, one focused on titles and abstracts and one on full texts. Both rounds will involve the testing of a screening protocol, guiding the decision making of individual researchers. Researchers will test each protocol independently on a sample of ten studies, compare results and discuss (a) the degree to which the protocol requires refinement, and (b) final decision making on the respective study. Protocols will then be refined and prepared for use with the remaining studies. Individual researchers will apply eligibility criteria independently and be blind to each other’s decisions about the in- or exclusion of publications. Disagreements between their individual judgements will be resolved by a third researcher.
Quality appraisal
All included publications will be assessed for their risk of bias using checklists developed by the Joanna Briggs Institute3 (JBI) for different study designs, including randomized controlled trials, qualitative and economic evaluations.
Data extraction
Pairs of researchers will independently extract data from 10% of the studies. Data extraction results will be compared, and disagreements discussed in our research team to achieve full consensus on how to approach data extraction among all research team members.
Individual researchers will extract data independently from remaining studies, and the extraction quality will be assured by the lead author. The following information will be extracted: study aim; study design; location; methods; study settings; study sample; CRC screening program characteristics; implementation stage; implementation framework use; study measures; implementation determinant information; implementation strategy information; implementation, service and other outcomes that are related to determinants and/or strategies; information needed to conduct risk of bias assessment (design dependent). Implementation strategy information extraction will be based on the “Prerequisites to Measuring Implementation Strategies” (PMIS) framework (27), recommending for implementation strategies to be specified by name, included components, actors, actions, action targets, temporality, dose, implementation outcome targets, and justification. To enable the coding process described below, both implementation determinant and strategy information will be extracted in the form of entire sentences and/or text sections included in original articles.
Should missing data be detected during data extraction, lead authors of papers will be contacted for unreported data and/or any other additional details of interest to the research team.
Data analysis
Findings will be synthesized narratively using the three stages of thematic synthesis (42): (1) Line by line coding; (2) the development of descriptive themes; and (3) the generation of analytical themes.
As part of the line-by-line coding of extracted information, information on the determinants to and strategies for implementing organized CRC screening programs will be coded using both deductive and inductive coding. The deductive coding of determinants will be guided by the Consolidated Framework for Implementation Research, CFIR (25) and that of implementation strategies by the Expert Recommendations for Implementing Change (ERIC) compilation of implementation strategies (43). The CFIR is a framework developed to build the knowledge base on quality implementation of complex interventions and contains five domains of factors potentially influencing implementation processes. These include the intervention, the individuals involved in an implementation, the inner and outer setting of the implementation, and the implementation process. The CFIR has been widely used by scholars to categorize and analyze determinants to colorectal cancer screening efforts, both as part of systematic reviews (32, 44, 45) and of primary studies (46–48). For this review, a recently updated version of the CFIR will be used based on information kindly shared by CFIR’s developers.
The ERIC compilation of implementation strategies(43) includes the description of 73 implementation strategies commonly acknowledged as relevant activities that, when used separately or in combination, can facilitate the integration of evidenced interventions into routine health care and prevention. While scholars have pointed to limitations in using the ERIC compilation as a coding tool(49, 50) due to a lack of granularity characterizing some of its strategies, it represents the most comprehensive and varied list of implementation strategies available for coding purposes. It has been applied in multiple health care focused systematic reviews (51–53). The parallel use of the PMIS framework(27) will further ensure that implementation strategies are thoroughly categorized and analyzed. Furthermore, the coding of strategies and determinants will also be inductive, allowing researchers to register any information not aligned with framework-based coding categories under the category “other”. Finally, researchers will be asked to develop brief memos of coding challenges related to framework use as they emerge, such that these can be addressed during regular team meetings.
Based on these considerations, a coding protocol will be developed. The coding protocol will be piloted by all members of the research team on a sample of five different studies. Researchers will identify potential limitations and needs for improvement individually and discuss these in a review team meeting to develop concrete steps for adjusting the coding protocol. The revised protocol will then be used for the coding of all included studies, with researchers having access to ad hoc support from other review team members and weekly research team meetings serving as an additional forum for problem solving around coding. These meetings will also be used to discuss inductive codes to enable decisions on whether to add new codes, and how to handle previously coded manuscripts.
To develop descriptive themes, two researchers will independently review the textual information retrieved for each code and develop descriptive themes by, e.g., identifying commonalities and differences in the ways in which implementation determinants and the use of implementation strategies are described; and by identifying how, e.g., different determinants, different strategies, and determinants and strategies are interlinked with each other. Descriptive themes will be based on the semantic level of texts, i.e., closely related to the language used in text excerpts. A summary of descriptive themes will be discussed among all members of the research team in two rounds – once at a preliminary stage to retrieve early input, and a second time to refine a more consolidated list of descriptive themes prior to their finalization.
In developing analytical themes, the research team will move to the latent level of meaning included in and across studies and build shared understandings of, e.g.,
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commonalities in determinants to the implementation of organized CRC screening programs and how they impact this implementation
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characteristics of implementation strategies used in the implementation of organized CRC screening programs
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commonalities and differences in strategies selected to address specific determinants
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linkages between determinants only, strategies only and determinants and strategies
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gaps in the current knowledge base for the implementation of organized CRC screening programs
Preliminary ideas for analytical themes will be mirrored in descriptive themes and discussed in the research team also considering review findings and the wider literature on organized CRC screening program implementation. Based on this discussion, two researchers will draft a first list of potential analytical themes for further input from and discussion among all review team members. This will lead to further refinement and the finalization of all analytical themes.
[1] An overview is available at https://www.swisscancerscreening.ch/de/angebote-in-ihrem-kanton
[2] Covidence systematic review software, Veritas Health Innovation, Melbourne, Australia. Available at www.covidence.org
[3] JBI’s repository of quality appraisal tools can be accessed here: https://jbi.global/critical-appraisal-tools