Azor‐Martinez 2016.
Study characteristics | ||
Methods | Randomised, controlled, and open study with an 8‐month follow‐up. The experimental group washed their hands with soap and water, together with using hand sanitiser, and the control group followed their usual handwashing procedures. Absenteeism rates due to URIs were compared between the 2 groups through a multivariate Poisson regression analysis. The per cent of days missed in both groups were compared with a z test. | |
Participants | A sample of 1341 (intervention group = 621, control group = 720) Inclusion criteria: children 4 to 12 years old, attending 5 state schools in Almerıa (Spain) whose parents/guardians had signed an informed consent document Exclusion criteria: children who had any of the following chronic illnesses that predisposed them to infection: neoplasia, primary and secondary immunodeficiencies, cystic fibrosis, chronic treatment with high doses of steroids or immunosuppressants |
|
Interventions | Hand‐washing workshops of 2‐hour duration. The experimental group washed their hands with soap and water together with using hand sanitiser, whilst the control group followed usual hand‐washing procedures. See Table 4 for details. | |
Outcomes | Absenteeism rates due to URIs Per cent of days missed Respiratory illness was defined by 2 of the following symptoms during 1 day, or 1 of the symptoms for 2 consecutive days: (1) runny nose; (2) stuffy or blocked nose or noisy breathing; (3) cough; (4) feeling hot or feverish or having chills; (5) sore throat; or (6) sneezing. A school absenteeism case (episode) was defined as when a child failed to attend school due to an URI. Common infectious illnesses, such as conjunctivitis, and skin infections were not included. Other causes for absenteeism, such as doctors’ appointments, family vacations, and accident injuries, were also excluded. No safety outcomes reported. |
|
Notes | Government funded | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | A random number table was used. |
Allocation concealment (selection bias) | Low risk | Schools/classes allocated prior to children recruited. |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Unblinded study |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Unblinded study |
Incomplete outcome data (attrition bias) All outcomes | High risk | Attrition levels high and different in the 2 groups |
Selective reporting (reporting bias) | Unclear risk | No protocol available |