Skip to main content

Motivations for participating in a clinical trial on an avian influenza vaccine

Abstract

In this study we describe the sociodemographic characteristics of people participating in a clinical trial on the safety and immunogenicity of a H5N1 influenza vaccine and we identify the main motivations for joining it.

Peer Review reports

Letter

Correspondence/Findings

Recently, the appearance of new influenza strains with the ability of propagating by human- human transmission put both the scientific community and the general public on alert [1, 2]. For this reason, the WHO underlines the urgency of developing vaccines to meet the new threat [3]. Knowing the characteristics and motivations of participants in clinical trials may help to improve the recruitment phase of future trials. Here, we describe the sociodemographic characteristics and motivations of people participating in a clinical trial of an influenza vaccine carried out in a university hospital.

The H5N1-008 trial (GlaxoSmithKline) was a multicenter phase III, double-blind, clinical trial conducted to compare the safety and reactogenicity of a monovalent H5N1 influenza vaccine with that of the licensed seasonal influenza vaccine Fluarix™ [4]. All healthy subjects aged ≥ 18 years were eligible for the trial. A total of 5,071 volunteers were recruited from 7 European countries between May and June 2006. Information on local and general symptoms was recorded by each subject using diary cards for the first seven days following each vaccination. Serious adverse events were recorded prospectively, ending at the last visit. The recruitment methods included talks, pamphlets and posters within and outside the hospital, medical faculties, outpatient clinics and other health areas. The study required four visits at the vaccination center of the hospital at days 0, 21, 42 and 180, and a blood extraction at each visit. Participants received two vaccinations at days 0 and 21 (pandemic vaccine or Fluarix™).

A cross-sectional study was carried out, in which all 383 recruits from our center were eligible to participate: on the last visit each participant was provided with a self-administered questionnaire of 12 items with closed answers on socio-demographic data, motivations for participating, how they learned of the trial, and others.

A total of 364 of 383 subjects (95%) answered the questionnaire. Characteristics of the participants are presented in Table 1. When our study population was compared to those who participated in seven European countries, no differences were found regarding age and education [4]. The most-common way of learning about the trial was word of mouth (70.1%; n = 255). Fifty-six (15.4%) subjects had participated in previous studies of vaccines or other drug trials. Eighty-seven percent (n = 318) of participants were willing to enroll in similar studies in the future, and 75.0% of the participants (n = 273) would wish to receive the vaccine if it were to be licensed by the European Medicines Agency and they had been in the control group.

Table 1 Basic characteristics of the study population

The most-frequently reported main motivation for joining the study was collaboration with science (n = 155; 42.6%), and it was related to several characteristics of participants (Table 2). It varied non-significantly according to gender (P = 0.11), and it was strongly related to their age (P < 0.001); participants older than 60 years were more likely to report collaboration with science than the younger age categories, while participants who reported economic reasons were mostly younger than 25 years of age. It also varied with the education level, the profession of participants, and the way in which people learned of the study (P = 0.06, 0.01 and < 0.001; respectively). Furthermore, age and the way of learning about the study were strongly related (P < 0.001).

Table 2 Characteristics of the participants by motivation to participate

Motivations for participating in clinical trials can be briefly summarized as follows: possibility of health benefits, obtaining information on the studied disease, willingness to contribute to scientific projects, trusting of specific physicians and economic interests [57]. Only 19 men and 38 women in our study reported participating to obtain protection against a possible influenza pandemic. These results are in accordance with a study of an HIV vaccine with healthy people, where only 12% of men and 22% of women agreed strongly that they were motivated by the possible protection against HIV [6]. Although it should be taken cautiously, our results highlight altruistic motives, with 40% of men and 45% of women reporting wanting to collaborate with science, in accordance with the literature [710]. Results show that one motivation for participation little explored in previous studies, the influence of other people, was an important factor. Most of the participants in our trial knew somebody related to the study, such as other participants who already had enrolled, and 37.6% reported this motivation for participating. Decisions regarding participation are strongly related to the social network of the subject: the attitudes, knowledge and habits of friends, relatives or colleagues regarding clinical trials influence the decision to join a trial. The small number of participants reporting economic reasons in our study was possibly related to the fact that the amount offered was low (100€), since it was meant to cover travel expenses. It predominantly appealed to younger people for whom the financial incentive was meaningful. Contrary, a review carried out among healthy volunteers found that financial reward was the principal reason for participation reported in 8 of 12 studies [10]. The fact that most of the subjects who chose the economic motivation were younger than 25 years shows an interesting link between the age of participants and their motivations. An open answer for other possible motivations was included in the questionnaire. However, only two people chose this option and in both cases the answer fell within the scope of the four proposed categories. The association between the way of learning about the study and the age of participants suggests that the recruitment method could appeal to people with different characteristics. This fact highlights the importance of taking the above into account while designing trials to avoid biased results.

In conclusion, the main reported motivation for participating was collaboration with science, and it was related to several characteristics of the participants. The strategies involved seemed to appeal to people with different demographics, underscoring the importance of the recruitment design in order to ensure generalizability of results.

References

  1. Campbell CN, Mytton OT, McLean EM, Rutter PD, Pebody RG, Sachedina N, White PJ, Hawkins C, Evans B, Waight PA, Ellis J, Bermingham A, Donaldson LJ, Catchpole M: Hospitalization in two waves of pandemic influenza A(H1N1) in England. Epidemiol Infect. 2010, 139: 1560-1569.

    Article  PubMed  Google Scholar 

  2. Beigel JH, Farrar J, Han AM, Hayden FG, Hyer R, de Jong MD, Lochindarat S, Nguyen TK, Nguyen TH, Tran TH, Nicoll A, Touch S, Yuen KY, Writing Committee of the World Health Organization (WHO) Consultation on Human Influenza A/H5: Avian influenza A (H5N1) infection in humans. N Engl J Med. 2005, 353: 1374-1385. Erratum in: N Engl J Med 2006, 354:884

    Article  PubMed  Google Scholar 

  3. Soborg C, Mølbak K, Doherty TM, Ulleryd P, Brooks T, Coenen C, van der Zeijst B: Vaccines in a hurry. Vaccine. 2009, 27: 3295-3298. 10.1016/j.vaccine.2009.02.030.

    Article  PubMed  Google Scholar 

  4. Rumke HC, Bayas JM, de Juanes JR, Caso C, Richardus JH, Campins M, Rombo L, Duval X, Romanenko V, Schwarz TF, Fassakhov R, Abad-Santos F, von Sonnenburg F, Dramé M, Sänger R, Ballou WR: Safety and reactogenicity profile of an adjuvanted H5N1 pandemic candidate vaccine in adults within a phase III safety trial. Vaccine. 2008, 26: 2378-2388. 10.1016/j.vaccine.2008.02.068.

    Article  PubMed  Google Scholar 

  5. Cheung AM, Lee Y, Kapral M, Scher J, Ho I, Lui-Yee D, Stewart DE: Barriers and motivations for women to participate in cardiovascular trials. J Obstet Gynaecol Can. 2008, 30: 332-337.

    Article  PubMed  Google Scholar 

  6. Colfax G, Buchbinder S, Vamshidar G, Celum C, McKirnan D, Neidig J, Koblin B, Gurwith M, Bartholow B: Motivations for participating in an HIV vaccine efficacy trial. J Acquir Immune Defic Syndr. 2005, 39: 359-364. 10.1097/01.qai.0000152039.88422.ec.

    Article  PubMed  Google Scholar 

  7. Halpern SD, Karlawish JH, Casarett D, Berlin JA, Townsend RR, Asch DA: Hypertensive patients' willingness to participate in placebo-controlled trials: implications for recruitment efficiency. Am Heart J. 2003, 146: 985-992. 10.1016/S0002-8703(03)00507-6.

    Article  PubMed  Google Scholar 

  8. Almeida L, Azevedo B, Nunes T, Vaz-da-Silva M, Soares-da-Silva P: Why healthy subjects volunteer for phase I studies and how they perceive their participation?. Eur J Clin Pharmacol. 2007, 63: 1085-1094. 10.1007/s00228-007-0368-3.

    Article  PubMed  Google Scholar 

  9. Nurgat ZA, Craig W, Campbell NC, Bissett JD, Cassidy J, Nicolson MC: Patient motivations surrounding participation in phase I and phase II clinical trials of cancer chemotherapy. Br J Cancer. 2005, 92: 1001-1005. 10.1038/sj.bjc.6602423.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  10. Stunkel L, Grady C: More than the money: a review of the literature examining healthy volunteer motivations. Contemp Clin Trials. 2011, 32: 342-352. 10.1016/j.cct.2010.12.003.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

The authors thank the reviewers of the manuscript for their helpful comments, Ferran Torres for statistical advisement and all those who took part in this study providing questionnaire data.

Funding

This research received no specific grant from any funding agency in the public, commercial or not-for-profit sectors.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Laura Costas.

Additional information

Competing interests

The authors have participated in investigations with GlaxoSmithKline and Sanofi Pasteur MSD vaccines (influenza vaccine and others).

Authors' contributions

LC and JMB conceived the study, and participated in its design. LC performed the statistical analysis and drafted the manuscript. BS and SL participated in the design of the study. MAM carried out the field work of the study. All authors read and approved the final manuscript.

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Reprints and permissions

About this article

Cite this article

Costas, L., Bayas, J.M., Serrano, B. et al. Motivations for participating in a clinical trial on an avian influenza vaccine. Trials 13, 28 (2012). https://doi.org/10.1186/1745-6215-13-28

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/1745-6215-13-28

Keywords