The proposed systematic review will be conducted in line with the JBI methodology for systematic reviews of effectiveness (27). We will also use the Preferred Reporting Items for Systematic review and Meta-Analyses (PRISMA) guidelines and its extension for protocols (PRISMA-P) (28) [see Additional file 1: PRISMA-P checklist].
Research Objective
This systematic review aims to evaluate the effectiveness of school-based interventions compared to non-intervention programmes in preventing tobacco smoking initiation among young people in LMICs.
Specifically, we will
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Assess the effect of a school-based intervention in preventing smoking initiation among young ones
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Assess the effects of the school-based intervention in reducing the smoking rate (reduction in the number of cigarettes smoke) Determine the effectiveness of the interventions based on their theoretical concepts.
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Determine effectiveness based on the mode of implementation (teacher-led or peer-led)
Review question
What is the effectiveness of school-based programmes classified by intervention type compared to no intervention in preventing tobacco smoking initiation among young people living in LMICs?
Inclusion criteria
The systematic review will consider studies that evaluate school-based interventions that prevent tobacco smoking initiation among in-school young people in LMICs compared to other non-intervention programmes. The primary outcome will be the non-initiation of tobacco smoking by the youth. Studies published in the English language from the year 2000 will be considered for the review to align with current trends of tobacco intervention programmes.
Participants
This review will consider studies that include in-school persons aged 10 – 24 years in LMICs.
Interventions
The review will consider studies that evaluate school-based interventions that aim at preventing tobacco smoking initiation, or tobacco use among young people who reside in LMICs. The types of interventions based on theoretical approaches such as only information of harmful effects of tobacco use, social influence, social competence, a combination of social influence and social competence or multimodal i.e., a combination of information, social influence, and competence will be considered. Furthermore, the approach to the administration of the intervention i.e. teacher-led, or peer-led, or researcher-led will be considered. Finally, the presence or absence of booster sessions will be considered.
Comparator
The review will consider studies that compare the intervention with non-intervention such as normal school education or the standard health education programmes taught in schools.
Outcomes
The review will consider studies whose outcome evaluates the smoking status of individuals or groups who reported tobacco non-use at baseline. The theoretical approach, mode of administration of interventions, and the presence or absence of booster sessions will be considered.
Effect sizes of the outcome would be measured by the rate/risk difference, rate/risk/odds ratio for categorical data and weighted/standardized mean difference for continuous data together with their 95% confidence intervals.
Type of studies:
This review will consider both experimental and quasi-experimental study designs including randomized controlled trials, non-randomized controlled trials, and before and after studies. Furthermore, analytical observational studies including prospective and retrospective cohort studies, case-control studies, and analytical cross-sectional studies will be considered for inclusion. Studies published in peer-reviewed journals in the English language from 2000 will be included in the review to align with current trends of tobacco intervention programmes.
Search Strategy
The search strategy will aim to locate both published and unpublished studies. An initial limited search of MEDLINE and CINAHL was undertaken to identify articles on the topic. The text words contained in the titles and abstracts of relevant articles, and the index terms used to describe the articles were used to develop a full search strategy for MEDLINE (PUBMED see Appendix #). The search strategy, including all identified keywords and index terms, will be adapted for each included information source. The reference list of all studies selected for critical appraisal will be screened for additional studies.
Information Sources
The databases to be searched include MEDLINE via Ovid, CINAHL via EBSCO, Embase, PsycINFO, PsycEXTRA, and the Cochrane Central Register of Controlled Trials. Sources of gray literature to be searched include ProQuest Dissertations and Theses, MedNar, EBSCO Open Dissertations, Open Access Theses and Dissertations, and Trove.
Study selection
Following the search, all identified citations will be ordered and uploaded into Mendeley (cite), and duplicates removed. Titles and abstracts will then be screened by two independent reviewers for assessment against the inclusion criteria for the review. Relevant studies will be retrieved and saved in full and their citation details imported into the JBI System for the Unified Management, Assessment, and Review of Information (JBI SUMARI; JBI, Adelaide, Australia)(29). The full text of selected citations will be assessed in detail against the inclusion criteria by two independent reviewers. Reasons for exclusion of full-text studies that do not meet the inclusion criteria will be recorded and reported in the systematic review. Any disagreements that arise between the reviewers at each stage of the study selection process will be resolved through discussion or with a third reviewer. The results of the search will be reported in full in the final systematic review and presented in the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA) flow diagram (30).
Assessment of Methodological Quality
Eligible studies will be critically appraised by two independent reviewers at the study level for methodological quality in the review using standardized critical appraisal instruments from the JBI for experimental, quasi-experimental, and analytical observational studies. Authors of papers will be contacted to request missing or additional data for clarification, where required. Any disagreements that arise will be resolved through discussion, or with a third reviewer. The results of the critical appraisal will be reported in narrative form and a table. All studies, regardless of the results of their methodological quality, will undergo data extraction and synthesis (where possible).
Data Extraction:
Data will be extracted from studies included in the review by two independent reviewers using the standardized data extraction tool within the JBI SUMARI (27). The data extracted will include specific details about the populations, study methods, interventions, intervention, and control/comparison groups and outcomes (incidence/rate/odds ratios, incidence/rate difference, weighted/standardized mean differences, etc.) of significance to the review objective. Any disagreements that arise between the reviewers will be resolved through discussion, or with a third reviewer. Authors of papers will be contacted to request missing or additional data, where required.
Data Synthesis:
Studies will, where possible be pooled in a statistical meta-analysis using JBI SUMARI. Effect sizes will be expressed as either odds/rate/risk ratios or incidence/rate differences (for dichotomous data) and weighted (or standardized) final post-intervention mean differences (for continuous data) and their 95% confidence intervals will be calculated for analysis. Heterogeneity will be assessed statistically using the standard chi-squared (Cochran’s Q test) and I squared tests. Statistical analyses will be performed using a random-effects model (31). Sensitivity and subgroup analyses will be conducted for 10 or more studies to assess the robustness of the methods used. Where statistical pooling is not possible the findings will be presented in the narrative form including tables and figures to aid in data presentation where appropriate. A funnel plot will be generated using RevMan V5 (Copenhagen: The Nordic Cochrane Centre, Cochrane) to assess publication bias if there are 10 or more studies included in a meta-analysis. Statistical tests for funnel plot asymmetry (Egger test, Begg test, Harbord test) will be performed where appropriate.
Assessing certainty in findings
The Grading of Recommendations, Assessment, Development and Evaluation (GRADE) approach for grading the certainty of evidence will be followed (32) and a Summary of Findings (SoF) will be created using GRADEPro GDT Version XX/updated in 2014McMaster University, ON, Canada) (33). The SoF will present the following information where appropriate: absolute risks for the treatment and control, estimates of relative risk, and a ranking of the quality of the evidence based on the risk of bias, directness, heterogeneity, precision, and risk of publication bias of the review results. The outcomes to be reported in the SoF will be non-initiation of tobacco smoking, the theoretical approaches employed in the intervention, the mode of administration of interventions, and the presence or absence of booster sessions.