The requirement for prior consent to participate on survey response rates: a population-based survey in Grampian
Open Access
- 18 November 2003
- journal article
- research article
- Published by Springer Nature in BMC Health Services Research
- Vol. 3 (1) , 21
- https://doi.org/10.1186/1472-6963-3-21
Abstract
A survey was carried out in the Grampian region of Scotland with a random sample of 10,000 adults registered with a General Practitioner in Grampian. The study complied with new legislation requiring a two-stage approach to identify and recruit participants, and examined the implications of this for response rates, non-response bias and speed of response. A two-stage survey was carried out consistent with new confidentiality guidelines. Individuals were contacted by post and asked by the Director of Public Health to consent to receive a postal or electronic questionnaire about communicating their views to the NHS. Those who consented were then sent questionnaires. Response rates at both stages were measured. 25% of people returned signed consent forms and were invited to complete questionnaires. Respondents at the consent stage were more likely to be female (odds ratio (OR) response rate of women compared to men = 1.5, 95% CI 1.4, 1.7), less likely to live in deprived postal areas (OR = 0.59, 95% CI 0.45, 0.78) and more likely to be older (OR for people born in 1930–39 compared to people born in 1970–79 = 2.82, 95% CI 2.36, 3.37). 80% of people who were invited to complete questionnaires returned them. Response rates were higher among older age groups. The overall response rate to the survey was 20%, relative to the original number approached for consent (1951/10000). The requirement of a separate, prior consent stage may significantly reduce overall survey response rates and necessitate the use of substantially larger initial samples for population surveys. It may also exacerbate non-response bias with respect to demographic variables.Keywords
This publication has 9 references indexed in Scilit:
- Obtaining valid response rates: considerations beyond the tailored design methodEvaluation and Program Planning, 2003
- Why we should not seek individual informed consent for participation in health services researchJournal of Medical Ethics, 2002
- Increasing response rates to postal questionnaires: systematic reviewBMJ, 2002
- Do Patient Consent Procedures Affect Participation Rates in Health Services Research?Medical Care, 2002
- Design and use of questionnaires: a review of best practice applicable to surveys of health service staff and patientsHealth Technology Assessment, 2001
- Selection Bias From Requiring Patients to Give Consent to Examine Data for Health Services ResearchArchives of Family Medicine, 2000
- Using patient-identifiable data for observational research and auditBMJ, 2000
- Health check-ups in general practice: a patient perspective.1996
- Complementary therapies in a local healthcare setting. Part I: Is there real public demand?Complementary Therapies in Medicine, 1996