The effect of a monetary incentive on return of a postal health and development questionnaire: a randomised trial [ISRCTN53994660]

Postal questionnaires are widely used to collect data in health research, but a poor response rate may reduce the validity and reliability of results. In a systematic review of randomised controlled trials of strategies to improve the response rate to postal questionnaires[1], a monetary reward had a significant effect on response. However, caution was attached to the interpretation of the findings in this review [2]. On further examination of the updated review 20% of the participants included in the analysis of the effect of inclusion of a monetary incentive in the final response came from healthcare settings [3] and none of the studies evaluated the use of monetary incentives for a postal questionnaire to collect data from a follow-up of a clinical trial. To evaluate the impact of such an intervention on response rate in such a setting we undertook a randomised trial.

The MRC ORACLE Children Study (MOCS) is following up nearly 9000 seven-year-old children whose mothers joined the MRC ORACLE Trial [4, 5] which evaluated the use of antibiotics to improve neonatal outcome after preterm labour or preterm rupture of the membranes. This trial of a monetary reward to enhance response to a postal questionnaire was undertaken between April 2002 – November 2003. Research Ethics Committee approval was obtained from the West Midlands Multicentre Research Ethics Committee

The questionnaire itself is 12 pages long and A4 in size. It contains questions relating to the child's health and development using a mixture of validated tools and questions pertinent to the study. In designing the study we implemented many of the strategies believed to influence response rates to postal questionnaires [1, 3]. The questionnaire itself is set out in a user friendly way and we have used coloured ink in its design. The letters accompanying the questionnaire are individualised to the child concerned and the parents are warned the questionnaire will be sent to them. The University in which MOCS is housed franks the envelope, the return envelope is stamped, and reminder letters include a questionnaire.

When a child in MOCS is seven years old the parents receive an information leaflet about the follow-up Study, and two weeks later a questionnaire about their child's health and development. Contact with parents has already been established prior to this. If no response is obtained the child's General Practitioner is contacted to check the child's address and ensure that contact would be appropriate. Six weeks after the first questionnaire, a reminder one is sent to those who have not responded. At this point the parents were randomly assigned by computer-generated allocation to receive a five-pound voucher (redeemable at many high street shops) with their mailed questionnaire or not (see Figure 1).

The sample size was predefined by the numbers not responding at this stage of the Study (i.e. approx 700). This yielded 80% power to detect an increased response from 10% to 18% or from 15% to 24% (at the 5% significance level).

Balance between voucher/not voucher groups on the main baseline covariates was good. 722 consecutive parents were randomly allocated to receive a voucher or not with the reminder questionnaire (see Table 1).

Inclusion of the voucher with the second questionnaire resulted in a 11.7% (95% CI 4.7% to 18.6%) improvement in the response rate between the two groups (χ² = 10.6, P = 0.001).

The inclusion of a five-pound voucher improved the proportion of questionnaires returned. MOCS will be completed in 2008 and a voucher is being sent to all parents with the reminder questionnaire. It is estimated that this will improve the response rate by 3% over the whole study, at a cost of £67 per additional questionnaire returned. This was calculated on the basis that vouchers will be sent to approximately 40% of parents (2842) and an additional 3% will return the questionnaire

This improvement in response rate, and hence of the validity and the reliability of results appears to be justified ethically and financially. This is particularly relevant in the follow up of children as there is some evidence [6] of raised levels of adverse outcomes in difficult to follow-up children.

SK and PB designed the trial. DJ and KP carried out the analysis. NM, AS, DT contributed to conception, design and interpretation. All authors read and approved the trial manuscript.