Vichayanrat 2012
| Methods |
Study design: quasi‐experimental Conducted in: Chon Buri Province, Thailand Unit of randomisation: subdistricts Unit of analysis: individual Setting: health centres and homes Funded by: Funding was not disclosed. However, study authors declared, "Lion (Thailand) and Colgate‐Palmolive (Thailand) Ltd and Diethelm & Co contributed toothbrushes and toothpaste for the study" Duration of the study: 1 year |
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| Participants |
Inclusion criteria: Children and their caregivers were included in the study if children were 6 to 36 months of age, and caregivers had no systemic disease and would routinely bring the child for vaccination Exclusion criteria: Children and their caregivers were excluded if they were unwilling to participate or did not complete the questionnaire Age at baseline: 6 to 36 months N (controls baseline): 52 N (controls follow‐up): 52 N (interventions baseline): 62 N (interventions follow‐up): 62 Recruitment: Experimental and control districts were selected on the basis of comparable population structure, caries prevalence and no existing oral health programmes at health centres Gender: not reported |
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| Interventions |
Interventions
Control: provision of toothbrushes and routine health care Duration of intervention: 1 year |
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| Outcomes | Dental caries (dmft) | |
| Implementation related factors |
Theoretical basis: self efficacy theory, health belief model and social support and organisational change theory Resources for implementation: lay health worker salaries, toothpastes and toothbrushes Who delivered the intervention: lay health workers PROGRESS categories assessed at baseline: parent’s occupation and family income and age PROGRESS categories analysed at outcome: not reported Outcomes related to harms/unintended effects: not reported Intervention included strategies to address diversity or disadvantage: not reported Economic evaluation: not reported |
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| Notes | ||
| Risk of bias | ||
| Bias | Authors' judgement | Support for judgement |
| Random sequence generation (selection bias) | High risk | No randomisation process was involved (quasi‐experimental design) |
| Allocation concealment (selection bias) | Unclear risk | Unclear |
| Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Unclear |
| Selective reporting (reporting bias) | Unclear risk | Unclear |
| Other bias | Unclear risk | Unclear |
| Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Unclear |
| Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Unclear |