Our systematic review and meta-analysis has been developed to assess the potential relationship between both sleep duration and sleep quality in relation to mental/psychological resilience across healthy paediatric and adult populations, drawn from the general population. Our findings are intended to inform healthcare providers, public health, education systems and the general population about the importance of sleep in relation to mental/psychological resilience, should we identify a relationship between these factors.
This protocol was designed in accordance with the preferred reporting standards for systematic review protocols (PRISMA-P), which have been previously established in the PRISMA-P administrative information checklist.(11) We applied for registration of our study protocol on 2 July 2020 with the international prospective register of systematic reviews (PROSPERO). The PROSPERO identification number is 191119.
Eligibility criteria
All components of participants, intervention, comparator, and outcome (PICO), consistent with PRISMA-P reporting guidelines(11), are as follows:
Participants
Our systematic review targets the inclusion of healthy humans drawn from the general population. Articles involving any of the following populations will be excluded:
- Animals;
- Infants (up to 12 months);
- Clinical populations including those with existing diagnosed sleep disorders, mental health disorders, and/or physical disabilities.
Intervention
Our systematic review is focused on the relationship between sleep duration/quality and mental/psychological resilience. No intervention/exposure is applicable for our review.
Comparator
Our systemic review is not comparing populations; therefore, we have no comparators.
Outcome
The primary outcome of our systematic review and meta-analysis is mental/psychological resilience.
Type of studies
We will screen and identify observational studies only and include cross-sectional, prospective and survey-based study designs. For studies that obtain information pertaining to sleep duration/quality and mental/psychological resilience but do not report on the direct relationship between the two variables, we will contact the corresponding author up to three times by email to request the data before excluding the full-text article. Published conference abstracts presenting original research data will also be included, based on recent recommendations.(12) Qualitative studies, case studies, protocol studies, questionnaire validation studies, experimental studies and in vitro/genetic studies will be excluded from the review. Furthermore, reviews of any kind, commentaries, editorials, reports, correspondence will not be eligible, unless they present original research data on the area of interest.
Information sources
A comprehensive, systematic search for literature will be conducted in June 2020, covering a total of eight academic databases (PubMed, Embase, PsycInfo, PsycArticles, CINAHL, Scopus, Web of Science and Academic Search Complete). Sources for grey materials will also be included. Pre-searches to identify relevant information sources and search terms were performed in March-June 2020. PubMed and PubMed’s MeSH terms were used to develop the search strategy and systematically identify relevant search terms.
Search strategy
A pre-screening of the preliminary result from PubMed was conducted as a support for finalizing the search strategy:
((resilience*[Title/Abstract] OR “mental toughness” [Title/Abstract] OR hardiness[Title/Abstract] OR flourishing [Title/Abstract] OR "Resilience, Psychological"[Mesh]) AND (sleep*[Title/Abstract] OR awake*[Title/Abstract] OR "Sleep"[Mesh]))
The PubMed search will be adapted and applied to included databases. The final search strategy will be developed by a medical librarian (LÖ) in close collaboration with subject specialists (TA, IG & MG). All search terms will be searched in a combination of the fields: “title”, “abstract” and in the “MeSH”/”thesaurus” when available. No filters or limitations will be added to ensure the inclusion of pre-indexed materials. All databases and grey sources will be searched from their inception to June 2020. Hand screening of reference lists for each included paper will be conducted. Experts in the field will also be contacted for any unpublished data which may be eligible for inclusion.
Study records
Data management
The records identified in the literature search will be uploaded to the systematic review software Covidence (Veritas Health Innovation, 2020) for automatic de-duplication and blinded screening. A search log with detailed search strings, source coverage, search dates, result and notes for all information sources will be appended to the review.
Selection process
Covidence software will be used to detect and exclude any duplications, which will be managed by LÖ. The remaining articles that potentially meet our eligibility criteria will first be screened by title and abstract by two independent reviewers (IG & AA). Articles will either be accepted or rejected by each of the two reviewers and any discrepancies will be resolved by a third reviewer (TA), based on the pre-defined inclusion/exclusion criteria described. Following title and abstract screening, the full text of the remaining articles will be sourced by LÖ and uploaded into Covidence software for review by the same two independent reviewers (IG & AA). Any discrepancies will be resolved by a third reviewer who has not been involved in the full text screening process (TA). Cabell’s Blacklist for predatory journals will be informed to confirm the scientific status of all included papers published in open access journals.
Data collection process
For articles that fulfil the pre-defined inclusion criteria, two authors (IG & TA) will independently extract relevant data using a data extraction sheet. Data extraction will be performed using Excel. In case of any discrepancies, a third reviewer (OMO) will resolve them by discussion until a consensus is reached. The final data extraction will also be overseen and checked by a statistician (OMO). The corresponding author of any article, where additional data needs to be obtained, will be contacted by email up to three times and responses will then be recorded and archived.
Data items
The data extraction sheet will encompass a range of information including the following:
- First author’s surname;
- Year of publication;
- Sample size;
- Country where study was conducted;
- Gender split;
- Age of the sample;
- Tool(s) used to assess resilience/hardiness/mental toughness (study outcome);
- Tool(s) used to assess sleep duration/quality;
- Confounders that were included for adjustment;
- Effect size reported for the relationship between sleep and resilience.
Risk of bias in individual studies
Risk of bias assessment will be performed by two reviewers (IG & TA). MG will later resolve any discrepancies through discussion until a consensus is reached. The Study Quality Assessment Tool for Observational Cohort and Cross-Sectional Studies from the National Institutes of Health,(13) or the Newcastle-Ottawa Scale for non-randomized studies(14) will be used to assess the quality and bias of included studies.
Data synthesis
The results of the included studies will be summarised in a table which depicts all of the data extraction information. Additionally, a detailed narrative synthesis of the findings will be written where we discuss methodology in detail along with discussing possible explanations for differences in effect sizes that are observed. A meta-analysis will be later conducted where the effect sizes from suitable studies are combined using a random-effects model. This will be conducted by the team’s statistician (OMO) to assess the strength of the body of evidence.