ArticleBMC health services research2007
When "no" might not quite mean "no"; the importance of informed and meaningful non-consent: results from a survey of individuals refusing participation in a health-related research project.
Article in BMC health services research, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 2 of them syntheses that pooled it.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
40 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- Non-pharmacological interventions to reduce the symptoms of mild to moderate anxiety in pregnant women. A systematic review and narrative synthesis of women's views on the acceptability of and satisfaction with interventions.Archives of women's mental health · 2020Pooled it
- Informed consent in dental care and research for the older adult population: A systematic review.Journal of the American Dental Association (1939) · 2017Pooled it
- Influence of Social Support on Patients' Adherence to Activity Advice in Low Back Pain: A Double-Blinded Randomised Controlled Trial.Physiotherapy research international : the journal for researchers and clinicians in physical therapy · 2026Trial
- Characteristics of participants consenting versus declining follow-up for up to 10 years in a randomized clinical trial.Clinical trials (London, England) · 2015Trial
- Trial
- Trial
- Exploring patients' reasons for declining contact in a cognitive behavioural therapy randomised controlled trial in primary care.The British journal of general practice : the journal of the Royal College of General Practitioners · 2012Trial
- Accrual and drop out in a primary prevention randomised controlled trial: qualitative study.Trials · 2011Trial
- Trial
- From Test Offer to Urologic Follow-up: Acceptability of Semen Analysis in Male Infertility and Preconception Care.Cureus · 2026Review
- Very Low Uptake in Workplace Semen Analysis Research: Formative Web-Based Cross-Sectional Follow-Up Survey Distinguishing Employees With Self-Reported Unawareness From Aware Nonparticipants.JMIR formative research · 2026Article
- Recruitment rates, retention rates, and follow-up completion in a Brief Intervention and Contact trial for suicidal behavior: a feasibility study.Pilot and feasibility studies · 2025Article
- Participant characteristics and reasons for non-consent to health information linkage for research: experiences from the ATHENA COVID-19 study.BMC medical informatics and decision making · 2024Article
- Asking informed consent may lead to significant participation bias and suboptimal cardiovascular risk management in learning healthcare systems.BMC medical research methodology · 2023Article
- Patient adherence to physical activity advice (PAPA) in patients with low back pain: Study protocol for a multicentre randomized controlled trial.Physiotherapy research international : the journal for researchers and clinicians in physical therapy · 2022Article
- Nonparticipation reasons in a randomized international trial of a new latent tuberculosis infection regimen.Clinical trials (London, England) · 2020Article
- A research tool for measuring non-participation of older people in research on digital health.BMC public health · 2019Review
- Patient perspectives on use of electronic health records for research recruitment.BMC medical research methodology · 2019Article
- Study design and characteristics of the Luxembourg European Health Examination Survey (EHES-LUX).BMC public health · 2018Article
- Women's experiences of being invited to participate in a case-control study of stillbirth - findings from the Midlands and North of England Stillbirth Study.BMC pregnancy and childbirth · 2018Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundLow participation rates can lead to sampling bias, delays in completion and increased costs. Strategies to improve participation rates should address reasons for non-participation. However, most empirical research has focused on participants' motives rather than the reasons why non-participants refuse to take part. In this study we investigated the reasons why older people choose not to participate in a research project.
methodsFollow-up study of people living in Tayside, Scotland who had opted-out of a cross-sectional survey on activities in retirement. Eight hundred and eighty seven people aged 65-84 years were invited to take part in a home-based cross-sectional survey. Of these, 471 refused to take part. Permission was obtained to follow-up 417 of the refusers. Demographic characteristics of people who refused to take part and the reasons they gave for not taking part were collected.
results54% of those invited to take part in the original cross-sectional survey refused to do so. However, 61% of these individuals went on to participate in the follow-up study and provided reasons for their original refusal. For the vast majority of people initial non-participation did not reflect an objection to participating in research in principle but frequently stemmed from barriers or misunderstandings about the nature or process of the project itself. Only 28% indicated that they were "not interested in research". The meaningfulness of expressions of non-consent may therefore be called into question. Hierarchical log-linear modelling showed that refusal was independently influenced by age, gender and social class. However, this response pattern was different for the follow-up study in which reasons for non-participation in the first survey were sought. This difference in pattern and response rates supports the likely importance of recruitment issues that are research and context specific.
conclusionAn expression of non-consent does not necessarily mean that a fully informed evaluation of the pros and cons of participation and non-participation has taken place. The meaningfulness of expressions of non-consent may therefore be a cause for concern and should be subject to further research. Many reasons for non-participation may be specific to a particular research topic or population. Information sheets should reflect this by going beyond standardised guidelines for their design and instead proactively seek out and address areas of concern or potential misunderstanding. The use of established behavioural theory in their design could also be considered.
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