This protocol is being reported in accordance with the reporting guidance provided in the Preferred Reporting Items for Systematic Reviews and Meta-Analysis Protocols (PRISMA-P) 2015 statement(16), and the checklist can be found in the additional File 1. This protocol will guide the review. If there is any modification of the protocol during the review, it will be informed and reasoned in the final manuscript. The review has been registered in the International Prospective Registry of Systematic Reviews (PROSPERO) with registration number 152562 (awaiting for publication).
2.1. Eligibility criteria
All studies that meet the following inclusion criteria will be included in the review: a) studies with adult population that present some type of ND in which dementia is the main symptom (Alzheimer's disease, frontotemporal dementia, body Lewydementia); b) studies that evaluate SC in any of its dimensions (theory of mind, emotional processing, social perception or attribution bias); c) observational studies, including cross-sectional, case-control and cohort studies; d) studies published in English or Spanish; and e) studies published in the last 10 years (October 2009-October 2019).
It should be noted that we will include all FTD types. This coversbvFTD and primary progressive aphasia (PPA), in its three variants: (i) non-fluent variant PPA (nfvPPA); (ii) semantic variant PPA (svPPA) (also called dementia semantic); and (iii) logopenic variant PPA (lvPPA)(17).
The following studies will be excluded from the review: a) those studies on populations with degenerative disorders in which dementia syndrome is not the main manifestation of the disorder (e.g.,dementia in Parkinson's disease, dementia in Huntington's disease, dementia in Wilson's disease ...); b) review or meta-analysis articles; c) single case studies, comments, books, conference papers, letters, editorials, theses and all those not peer-reviewed (grey literature).
2.2. Search strategies and data source.
To establish the search strategy necessary to identify all relevant articles, an expert librarian from the Marqués de Valdecilla University Hospital (Santander, Spain) was consulted. The systematic search was carried out in the following databases: MEDLINE database via Pubmed, Cochrane Library, Lilacs, Web of Science (WoS) and PsycINFO. Appropriate search terms were used, that is, MeSH terms and when this was not possible.Free text was considered using keywords related to dementia and SC. The detailed search strategy can be found in Additional File 2. A manual search of reference lists of articles identified as eligible will be performed. All studies published in English or Spanish between October 2009 and October 2019 will be taken into account.
2.3. Study Selection
All the references found in the different databases that responded to the search criteria were imported into the EndNote (software) program (Clarivate Analytics, Philadelphia, USA), which eliminated duplicate citations. The work team made up of four reviewers (ESS, NMG, MSR and GAF) will independently evaluate each of the selected titles and abstracts according to the eligibility criteria. The full texts of potentially relevant articles will be retrieved and revised again. Each study will be reviewed by at least two reviewers. The final decision regarding the inclusion of studies will be made based on a thorough review of the full articles by two reviewers. In case of discrepancies, these will be evaluated by the entire team, as well as by a senior researcher (RAA). The result of the selection process will be reported in a PRISMA flow diagram (18).
2.4. Assessment of risk of bias of primary studies
Reviewers will perform the risk of bias assessment of each selected article. Each study will be evaluated by at least two reviewers independently and discrepancies will be resolved by the full review team. The evaluation process will be carried out using the Joanna Briggs Institute (JBI) Critical Evaluation Checklists(19). Because the type and propensity for bias of the different studies varies depending on the design of each one, the following checklists will be used: a) JBI critical appraisal checklist for analytical cross-sectional studies; b) JBI critical appraisal checklist for case-control studies; and c) JBI critical appraisal checklist for cohort studies. A summary of the assessment of risk of bias of the studies will be provided through tables.
2.5. Data extraction
A registry has been designed for data extraction among all members of the review team. The following information will be extracted from all included studies: author, year of publication, location, N, population (type of ND), type of study, mean age, domain of SC evaluated, summary of results, follow-up period (if corresponds), and data from the healthy control group (if applicable). The data extraction task will be carried out among the team members and each article will be reviewed by at least two reviewers independently. If necessary, the authors of the articles will be contacted to collect data that are not available in the manuscript.
During the data extraction process, the consensus of the entire team will also be used in case of discrepancies before reaching a final decision.
2.6. Data synthesis
A narrative synthesis of all the studies included in the review will be carried out and the relevant data from the studies will be presented in a table. The data will be grouped according to the different types and subtypes of ND, and within these groups we will try to synthesize the results attending to the different domains of the SC, as far as possible.