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BMJ 2005;330:178 (22 January), doi:10.1136/bmj.38309.664444.8F (published 16 December 2004)
Michael Watson, lecturer in public health1, Denise Kendrick, senior lecturer2, Carol Coupland, senior lecturer in medical statistics2, Amanda Woods, senior research fellow2, Deb Futers, professional lead: health visiting3, Jean Robinson, head of information4
1 Faculty of Medicine and Health Sciences, School of Nursing, University of Nottingham, Queen's Medical Centre, Nottingham NG7 2HA, 2 Division of Primary Care, University of Nottingham, Nottingham NG7 2RD, 3 Rushcliffe Primary Care Trust, Nottingham NG2 6BT, 4 Nottingham Health Informatics Service, Nottingham City Primary Care Trust, Nottingham NG1 6GN
Correspondence to: M Watson michael.watson{at}nottingham.ac.uk
Design Randomised controlled trial.
Setting 47 general practices in Nottingham.
Participants 3428 families with children under 5.
Intervention A standardised safety consultation and provision of free and fitted stair gates, fire guards, smoke alarms, cupboard locks, and window locks.
Main outcome measures Primary outcome measures were whether a child in the family had at least one injury that required medical attendance and rates of attendance in primary and secondary care and of hospital admission for injury over a two year period. Secondary outcome measures included possession of safety equipment and safety practices.
Results No significant difference was found in the proportion of families in which a child had a medically attended injury (odds ratio 1.14, 95% confidence interval 0.98 to 1.50) or in the rates of attendance in secondary care (incidence rate ratio 1.02, 0.90 to 1.13) or admission to hospital (1.02, 0.70 to 1.48). However, children in the intervention arm had a significantly higher attendance rate for injuries in primary care (1.37, 1.11 to 1.70, P = 0.003). At both one and two years' follow up, families in the intervention arm were significantly more likely to have a range of safety practices, but absolute differences in the percentages were relatively small.
Conclusions The intervention resulted in significant improvements in safety practices for up to two years but did not reduce injuries that necessitated medical attendance. Although equipment was provided and fitted free of charge, the observed changes in safety practices may not have been large enough to affect injury rates.
The high cost of safety equipment and the difficulty of installing it have been identified as barriers to families implementing advice on home safety.3 No trials have examined the provision and fitting of equipment free of charge.
We report the main results of a randomised controlled trial assessing the effectiveness of an intervention in increasing safety practices and reducing unintentional injuries in families with children aged under 5 years, living in deprived areas.
Our study population comprised families with one or more children younger than 5 years from the caseloads of participating health visitors. We did not invite families in which one or more children were on the Child Protection Register or a child had experienced a fatal unintentional injury.
Interventions
The intervention comprised a standardised consultation by a health visitor individualised and specific to the children's ages in each family.
The health visitors offered stair gates, fire guards, smoke alarms, cupboard locks, and window locks free of charge to low income families in the intervention arm, and these were fitted free of charge. We defined low income families as those receiving means tested benefits. Families not on a low income were offered equipment at cost price and a delivery service to their home.
Families randomised to the control arm received usual care. They did not have access to the research documentation, free or low cost safety equipment, or the fitting scheme.
Outcome measures
Primary outcome measures were whether a child in the family had at least one medically attended injury and the rates of attendance in primary and secondary care and of hospital admission for injury during the two year follow up period. We obtained these data from the primary and secondary care records for all children aged under 5 at the start of the trial and for new births during the study period. Secondary outcome measures included severity of injury assessed from primary and secondary care records. We assessed possession of safety equipment, safety practices, self reported injury, and satisfaction with the intervention, at 12 and 24 months' follow up by two postal questionnaires to separate random samples of 1000 families from each treatment arm. We validated responses to the 12 month questionnaire. We obtained baseline data on sociodemographic characteristics, possession of safety equipment, and safety practices from a postal questionnaire. We assessed satisfaction among health visitors with the intervention by postal questionnaire at the end of the intervention period.
Randomisation and blinding
Randomisation took place after the baseline questionnaires had been returned. We stratified participants by health visitor and randomised them to treatment arms.
It was not possible to blind participants, and health visitors were aware of which clients were in the intervention arm, but they were not provided with a list of controls so contamination was minimised. We kept outcome assessors blind to the treatment arm of the families.
Sample size and statistical analysis
We estimated that a sample size of 3400 families, 1700 in each arm, would give 80% power to detect at the 5% significance level a relative reduction of 10% in medically attended injuries between treatment arms.
We used multilevel logistic regression to compare whether at least one child in the family had one or more medically attended injuries and whether family safety practices varied between treatment arms. We compared injury rates using multilevel Poisson regression and examined the effect of compliance by comparing outcomes of participants in the intervention arm with those in the control arm. We studied interactions between the intervention and family income and child age (see bmj.com).
A total of 1163 (68%) families in the intervention arm received the safety consultation, and 619 families (36%) had free equipment fitted, and 26 (1.5%) bought equipment at low cost. The attendance rate for injury in primary care was higher (by 37%) for children in the intervention than in the control arm (P = 0.003) (table 1). We found no evidence that the effect of the intervention varied by family income or child age for any of the primary outcome measures (P > 0.1 for all interaction terms). A compliance analysis found similar results to the primary analysis, with a higher injury attendance rate in primary care in children in the intervention arm who received the safety consultation than in children in the control arm (incidence rate ratio 1.50, 95% confidence interval 1.21 to 1.88) but no difference in rates of attendance in secondary care or admission to hospital.
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Table 2 shows that at one year and two years, families in the intervention arm were significantly more likely to have a range of safety practices. Absolute differences in the percentages of families with safety practices were relatively smallnone exceeded 10%.
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Among families responding to the 12 month questionnaire, 89% (286/322) of those receiving equipment agreed or strongly agreed that they were satisfied with the safety equipment, and 70% (411/589) of families who received the consultation agreed or strongly agreed that they were satisfied with the health visitor's advice. Ninety five per cent (53/56) of responding health visitors agreed or strongly agreed that the safety consultation should be used in routine practice.
Limitations of the study
Only 35% of eligible families invited to participate in the trial did so. Although this is not a particularly low recruitment rate for a trial set in a deprived area, it may limit the generalisability of our findings as participants may have been families most motivated to make their homes safer.
It was not possible to keep health visitors completely blind to the identity of families in the control arm. However, this is unlikely to explain our findings; firstly, we measured the provision of safety advice in routine child health clinics before and after the trial started and did not find an increase; secondly, the fitting of equipment should have reduced the potential for its transfer between families in the two treatment arms; and thirdly, increases in possession and use of safety equipment in the control arm over the two year follow up period were small.
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Our inability to blind families participating in the study may have led to differential over-reporting of safety practices, but our use of validated questions on safety practices should have minimised this. In addition, the primary outcome measures were not self reported but ascertained by blinded assessors.
Finally, 548 (32%) intervention arm families did not receive the safety consultation, and only 645 (38%) received safety equipment. This will have limited the potential for the intervention to show an effect. However, the compliance analysis found similar results to the main analysis, implying that families who had the consultation had similar injury rates to those who did not.
Strengths of the study
Our study was adequately powered to detect a 10% reduction in medically attended injuries; allocation concealment was adequate; and we used an intention to treat analysis.
To our knowledge this trial had a longer follow up period than previous studies and achieved follow up on a high proportion of families. We used home observation to validate the questions used to measure self reported safety practices and found the questions to have high sensitivity and specificity. Importantly, both the families who had the intervention and the health visitors who delivered reported high degrees of satisfaction with the safety consultation.
Comparison with other studies
Our findings are consistent with previous systematic reviews in terms of possession and use of safety equipment, safety practices, and injury outcomes.1-4 Only three previous studies that provided free or discounted safety equipment in a clinical setting have used occurrence of injury as an outcome measure. One trial found a reduction in self reported injuries,5 but none found a reduction in medically attended injuries, ascertained from medical records.5-7
Interpretation of the findings
The increased possession and use of safety equipment among families in the intervention arm did not translate into a lower injury rate. A higher than expected number of families living in a deprived area possessed safety equipment at baseline. Consequently, the absolute differences between treatment arms in the percentages of families with safety practices were relatively small, and a greater difference in safety practices may be required to affect the occurrence of injury. It is also possible that safety practices are not associated with reduced injury rates, but this is less plausible as several observational studies have shown a lower risk of injury among people with a range of safety practices.
Several explanations are possible for the higher attendance rate in primary care among intervention arm children. Firstly, participation in the intervention arm of the trial may have raised parents' awareness and changed their consulting behaviour for more minor injuries. Secondly, risk compensation8 may have occurred.
Implications for injury prevention practice and future research
Our findings in relation to safety practices and degrees of satisfaction are encouraging. However, our findings also highlight the importance of rigorously evaluating the widespread provision of equipment not only in terms of safety practices but also in terms of injury outcomes and uptake of schemes by those most at risk. Very large trials are required, or well designed case-control studies or cohort studies to examine the protective effect of specific items of equipment, followed by randomised controlled trials.
This is the abridged version of an article that was posted on bmj.com on 16 December 2004: http://bmj.com/cgi/doi/10.1136/bmj.38309.664444.8F We thank the families who took part in the study and the health visitors, nursery nurses, and doctors who supported the study. We are also indebted to Sarah Ross for tracking trial participants and identifying new births.
Funding: NHS Executive, Trent. DK was funded by a Department of Health Public Health Career Scientist Award. AW was funded by a Department of Health Primary Care Researcher Development Award.
Competing interests: None declared.
Ethical approval: Queen's Medical Centre Research Ethics Committee.
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