- Research article
- Open Access
- Open Peer Review
Strategy for recruitment and factors associated with motivation and satisfaction in a randomized trial with 210 healthy volunteers without financial compensation
BMC Medical Research Methodologyvolume 15, Article number: 2 (2015)
The aim was to describe a strategy for recruitment of healthy volunteers (HV) to a randomized trial that assessed the efficacy of different telephone techniques to assist HV in performing cardiac massage for vital emergency. Participation in the randomized trial was not financially compensated, however HV were offered emergency first-aid training. We also studied factors associated with HV motivation and satisfaction regarding participation in the trial.
Strategy for recruitment of 210 HV aged 18 to 60 years was based on: (1) the updated records of all telephone number since January 2000 of HV registered in the Rouen Clinical Investigation Centre HV database, (2) a communication campaign for the general public focussing on posters and media advertisements. Data on the recruitment, socio-demographics, motivation and satisfaction of the 210 HV were collected by anonymous self-administered questionnaire.
Of the 210 HV included, 63.3% (n = 133) were recruited from the HV database and 36.7% (n = 77) by the communication campaign. On the one hand, the HV database enabled screening of 1315 HV, 54.8% (n = 721) of whom were reached by phone, 55.2% (n = 398) of these latter accepted to participate in the study and 10.1% of the initial screening (n = 133) were finally included. One the other hand, for the 77 HV not recruited from the HV database, word-of-mouth (56.1%) was the main means of recruitment. The male/female ratio of the 210 HV was 0.5 and mean age 43.5 years (Standard Deviation = 12.4). The main motivations given for participating in the trial were to support research (87.6%) and receive emergency first-aid training (85.7%). Overall satisfaction with the welcome process was significantly higher for older HV (46–60 years) (adjusted odds ratio (AOR): 3.44; 95% confidence interval (95% CI): 1.48-7.99), and for HV in management jobs (AOR: 4.26; 95% CI: 1.22-14.87). Satisfaction with protocol management was higher for women (AOR: 2.33; 95% CI: 1.18-4.60) and for older HV (46–60 years) (AOR: 4.76; 95% CI: 1.97-11.52).
Recruitment of non-compensated HV required broad screening with a primary HV database alongside word-of-mouth communication which seemed more efficient than media advertising. To enhance HV recruitment to randomized trials without financial compensation it seems crucial to provide them not only with a direct interest but also to ensure their satisfaction.
Clinical trials require recruitment of patients and healthy volunteers (HV). The willingness of the general public to participate in clinical trials seems low. Ohmann et al.  found that only 25% of 225 visitors interviewed at a German University accepted taking part in clinical trials, with a likelihood of lower participation in surgical trials than in dental or pharmaceutical trials. Patients with cancer are often motivated to participate in order to gain possible therapeutic benefits, with pressure of growing cancer, and from study investigators and relatives [2–6]. Nevertheless, these patients also participate in helping future patients and contribute to science [3, 5, 7], especially if their prognosis is poor . Patients with non-cancer diseases are largely motivated by expectation of personal benefit [8, 9] or obtaining ancillary care provided by clinical trials . Altruism is also a motivation [11–17]. Moreover clinical trials also require the participation of HV, especially for phase I. The recruitment of HV is generally facilitated by providing monetary incentives [18, 19] and the main reported motivation of HV is frequently financial reward [20–26]. Kass et al.  investigated study participation in the USA and reported that for HV, money was a good aspect for 55% and the best aspect for 46%. But many others motivations are described by HV, such as contributing to science, helping others or personal benefits [26–29]. Few studies have been conducted in HV without financial compensation, due to funding constraints or ethical considerations. Indeed payment of HV is still discussed among volunteers: Russel et al.  found that a minority of Canadian HV agreed with paying research subjects. This is also discussed in the scientific community, as some authors think that money might encourage misrepresentation and the participation of disadvantaged or vulnerable persons [21, 26, 30]. Resnik  reviewed limits on risks in studies and reported that financial compensation should not be a justification for increased risk. The current dominant view is that only time and expenses should be compensated . However without financial compensation, recruitment can be difficult. In fact, more than 50% of clinical trials require an extension because of recruitment issues and more than one-third do not achieve their original recruitment target , even if financial compensation is given. Moreover, to our knowledge, no study to date has reported the demographic characteristics, recruitment process, or motivation and satisfaction levels of HV who participated without financial compensation. The aim of the present study was to describe a strategy for recruitment of healthy volunteers (HV) to an interventional study without financial compensation, and to identify factors associated with the motivation and satisfaction of these HV.
The present study is ancillary to a randomized trial conducted in 2013 at the Clinical Investigation Centre (CIC) of Rouen University Hospital, France. This randomized trial had assessed the effectiveness of three telephone techniques to assist untrained volunteers in performing cardiac massage in vital emergency situations . Randomization was performed by sealed envelopes and HVs were allocated into one of the three tested telephone assistances: 1- telephone assistance with the order to perform cardiac massage then hang up (control group); 2- continuous telephone assistance with an emergency regulating doctor; 3- telephone assistance with the order to perform cardiac massage then continuous guidance by a sound pacer. On the same day, the HV signed the informed consent document, was then randomized and after performed the intervention (no follow up). Then the HV performed continuum cardiac massage on a manikin during 5 minutes. The end-point of the baseline randomized trial was the effectiveness of the thoracic compression (frequency and depth). Afterwards, in order to offer a benefit and thank HVs, they received a brief emergency first-aid training session free of charge by a nurse (about 30 minutes). The randomized trial protocol was approved by the local Ethics Committee (Comité de Protection des Personnes Nord-Ouest I n° 2012/029, approved December 14, 2012). The number of subjects required was calculated for the randomized trial with a significance level of 2.5% and a power test of 80% . The baseline randomized trial required recruitment of 210 non-financially compensated HV and was conducted for 7 days between September and November 2013 at the CIC. The CIC managed recruitment of the HVs required, and assessed the strategy for recruitment as well as the motivation and satisfaction of the HVs. The present study reports the results of this assessment. The CIC is authorised to conduct interventional studies with HV.
Only healthy volunteers age from 18 to 60 years were eligible for inclusion. Non-inclusion criteria were: current employment or volunteering as rescuers (fire fighters, ambulance attendants or first aid volunteers), emergency first-aid training within 12 months of the study or rescuer, physical or mental disability, medical contraindication to physical exertion, low proficiency in French language, pregnancy or breastfeeding, or legal protection (curatorship or guardianship).
The first stage in the recruitment process of HV was the use of the Rouen CIC database: “Logic CIC”, (Oriam® eTM@V3). Logic CIC is a software programme which is specially designed by the French National Institute of Health and Medical Research (INSERM) to assist CICs in France in managing their own HV database. Healthy volunteers wishing to participate in medical research protocols are registered in this database with their demographic characteristics (last name, first name, gender, date of birth, place of birth, profession), life-style characteristics (contraception, smoking, alcoholism) and their contacts (address, telephone numbers). Our registration of HV began in January 2000 and included an overall 1500 HV at the moment of extraction. The database is updated when HVs self report any changes and when participating in a study. The database was declared to the National Commission on Informatics and Liberty (Commission Nationale Informatique et Libertés N° 1383369). Logic CIC allows selection of HVs according to their demographic and life-style characteristics, and contacts. Recruitment for the baseline randomized trial was based on extraction of the mobile and land line telephone numbers of all HV aged 18 to 60 years registered in Logic CIC on August 27, 2013. We attempted to contact by telephone all HV extracted from Logic CIC and proposed participation in the study to those HV successfully contacted. The randomized trial was presented as medical research on emergency first aid, with an emergency first-aid training session. If participation in the study was declined, the reason for refusal was requested by an open-ended question, the answer to which was retrospectively categorized as “HV not available”, “no financial compensation”, “other” or “reason not given”. If the HV agreed to participate and was available during the proposed period (appointments between 8:30 and 16:30), non-inclusion criteria were checked by telephone, starting with “emergency first-aid training within 12 months of the study or rescuer”, then “physical disability”, then “medical contraindication to physical exertion”. As soon as one non-inclusion criterion was reached, no further questions were asked. The criteria “mental disability” and “legal protection” were not asked by telephone. The criterion “low proficiency in French language” was evaluated, and some pregnancies were spontaneously reported by HV. In absence of non-inclusion criteria, an appointment was given for the inclusion visit at the CIC. Other methods of communication were used to recruit the 210 HV: posters (in Rouen: university hospital, faculty of medicine, faculty of law, local businesses), a message on Rouen University Hospital’s website, in newspapers (local daily newspaper), on radio and on social networks (Facebook, Twitter).
HV were included in the study after interview at the CIC, verification of selection criteria and signature of consent. They then participated in the trial on the same day (one visit: information, inclusion, intervention). After the intervention (cardiac massage), the HV completed an anonymous self-administered questionnaire. Demographics were collected on gender, age and socio-professional category, classified as follows: without professional activity (unemployed, inactive or retired), student, farmer, blue-collar worker, employee, middle-level activity (mid-level profession, shop keeper, craftsman or business owner) and manager/intellectual profession. Information’s source of the study’s conduct were collected: word-of-mouth, posters, Rouen University Hospital website, newspapers, radio, social networks, and others (several answers possible). The HV not registered in Logic CIC database were those recruited by these other communication strategies. Participation in other clinical trials and motivation to participate in the present study were: to support research, learn about emergency first-aid, update knowledge of emergency first-aid, curiosity, interest in medical research results, protocol without risk (no needle, no drugs etc.), and other choices (several answers possible). Prospects for HV participation were also collected: participation in a new medical research study, recommendations for relatives to participate in a new medical research study, interest in possibility of consulting the research protocols proposed by the CIC on the Internet and to register directly online (5-item Likert scale: “strongly disagree” to “completely agree”). Some data were not reported by HV (gender, age, socio-professional category, motivation, satisfaction, participation outlook). Thus we have indicated the maximal number of respondents to every question.
Satisfaction on the overall welcome at the CIC was measured by 5-item Likert scale (0: “unsatisfied” to 4: “very satisfied”) for each of the following items: directions given by the staff for finding the CIC, ease in finding the CIC, rapidity of greeting on arrival at the CIC, cleanliness of the premises. An overall satisfaction score of the welcome was obtained by summing the 4 items (score from 0 to 16). Satisfaction to the protocol management was also measured by a 5-item Likert scale (0: “unsatisfied” to 4: “very satisfied”) for each of the following items: explanation of the research interest by the physician, explanation of protocol organisation by the staff, time for reflection suggested by the physician between information form and consent signature, physician’s explanation of benefits and risks of the study, confidentiality during the study. An overall satisfaction score of the protocol management was obtained by summing the 5 items (score from 0 to 20).
Age was categorized into three groups for analyses (18–30, 31–45 and 46–60 years). The age cut-offs were chosen to form approximately equal periods of time (about 15 years for each age group). In our study, the median was high for the satisfaction scores related to overall welcome and protocol management. Satisfaction scores were dichotomized into two classes according to the median: not fully satisfied HV (score below or equal to the median) and fully satisfied HV (score above the median). Percentages were used to describe HV responses. There were some missing data (i.e. no response to items in the self-administered questionnaire by the 210 HV): 7 on gender, 8 on age, 10 on socio-professional category, 4 on overall satisfaction with the welcome process and 10 on satisfaction with protocol management. Chi-square tests were conducted to determine differences in categorical data and chi-square tests for linear trend (extended Mantel-Haenszel) to analyse the variables according to age. We performed two multivariate analyses to identify factors associated with full satisfaction using logistic regression for each of the two satisfaction scores (Overall welcome satisfaction and Protocol management satisfaction) as dependant variables (two classes: not fully satisfied or fully satisfied HV). Factors with a p value lower than 0.30 (gender, age, socio-professional category and registration status in Logic CIC database) were included in the multivariate analysis and a p value lower than 0.05 was considered to be significant. Statistical analyses were performed using StatCalc Epi Info® 7.
The telephone numbers of 1315 HV aged 18 to 60 years were extracted from Logic CIC database. The male/female ratio was 1.3. The number of HV at each stage of recruitment is shown in the flow chart (Figure 1). Of the 1315 HV, 133 were finally recruited for the randomized trial (10.1%, 95% CI: 8.5 – 11.7). Table 1 shows the demographics of HV registered in Logic CIC database at the three main stages of recruitment. Greater age of HV was associated with easier contact by telephone (358/776, 46.1% of under 30 year old HV; 112/180, 62.2% of 31 to 45 year old HV and 250/354, 70.6% of 46 to 60 year old HV; p < 0.001). Overall, 133 of the 210 HV (63.3%) included in the intervention study were recruited by this process. Five HV did not report their registration in the anonymous self-administered questionnaire. Of the 82 HV who had declared they were not registered in Logic CIC database, the main source of information was word-of-mouth (46/82 HV, 56.1%). Sources of information according to gender and age are reported in Table 2. Word-of-mouth was most frequently reported by younger HV (22/29, 75.9% of under 30 year old HV; 9/23, 39.1% of 31 to 45 year old HV and 13/27, 48.2% of 46 to 60 year old HV; p = 0.02).
Description of HV included
The male/female ratio of the 210 HV included was 0.5 and mean age was 43.5 years (Standard Deviation = 12.4). Age groups were: under 30 years (34.7%), 31–45 years (25.2%) and 46–60 years (40.1%). HV were: without professional activity (12.5%), students (15.5%), blue-collar workers (5.0%), employees (40.5%), mid-level professions (13.5%) and managers/intellectual professions (13.5%). There were no farmers. Ninety-seven HV (46.2%) had already participated in a medical research study.
Motivation of HV included
The motivations of the HV participating in the study are presented in Table 3. The main motivation was supporting medical research, reported by 87.6% (184/210) of HV. Emergency first-aid training (“learning about emergency first-aid” or “updating knowledge on emergency first-aid”) was reported by 85.7% (180/210) of the HV. Supporting medical research was reported significantly more by women (54/68, 79.4% of men and 123/135, 91.1% of women; p = 0.02) and by Logic CIC database registered HV (67/82, 81.7% of unregistered HV and 117/128, 91.4% of registered HV; p = 0.04). Interest in medical research results was more frequently reported by older HV (18/70, 25.7% of under 30 year old HV; 14/51, 27.5% of 31 to 45 year old HV and 40/81, 49.4% of 46 to 60 year old HV; p = 0.003) and curiosity by younger HV (31/70, 44.3% of under 30 year old HV; 14/51, 27.5% of 31 to 45 year old HV and 21/81, 25.9% of 46 to 60 year old HV; p = 0.01).
Satisfaction of HV included
Reponses for each satisfaction item on the self-administered questionnaire are shown in Figure 2. Median, minimum, and maximum satisfaction scores for the overall welcome were 15, 10 and 16 (out of 16) respectively. This satisfaction score differed significantly according to age (p = 0.001) but not to gender or registration in Logic CIC database (Table 3). After multivariate analysis (Table 4), HV aged 46–60 years and managers/intellectual professions were significantly more satisfied with the overall welcome, with respectively AOR: 3.44, 95% CI [1.48 - 7.99] and AOR: 4.26, 95% CI [1.22 - 14.87]. Median, minimum, and maximum satisfaction scores for protocol management were 19, 11 and 20 (ouf of 20) respectively. This satisfaction score differed significantly according to gender (p = 0.03) and age (p < 0.001) (Table 3). After multivariate analysis (Table 4), women and HV aged 46–60 years were significantly more satisfied with the protocol management, with respectively AOR: 2.33, 95% CI [1.18 - 4.60] and AOR: 4.76, 95% CI [1.97 - 11.52].
Recruitment process of HV
The HV database of the CIC of Rouen (Logic CIC) was large and allowed extraction of telephone numbers of 1315 HV aged 18 to 60 years. The rate of recruitment by this HV database was 10.1% and represented 63.3% of the total sample required demonstrating the value of such a database for recruitment of HV. Greater age of HV was associated with easier contact by telephone. An assumption may be that young HV more likely had a mobile telephone, providing more difficulties to reach them than with a land line, because of number changes or technical problems such as regional coverage. Pitrou et al.  found that French people using only mobile telephones were under 40 years and that study participants contacted on their mobile telephone appeared to be less easily reachable than by land line. This possible confounder is minimized because the telephone numbers provided by HV to register on Logic CIC database were the numbers which were the easiest reachable.
Furthermore in our study, the main reason given by HV who had been successfully contacted for their refusal to participate was lack of availability during the proposed time slots. Logistical issues appeared as a major obstacle in recruitment, such as inability to take extra time off work for research appointments . Moreover the appointment reliability of HV was also problematic: in our study, 35.1% of HV with an appointment did not attend and some without advance warning. Thus the study which was initially planned to last 5 days, finally required 7 days.
Word-of-mouth was the main source of information for HV not recruited by database, highlighting the importance of satisfied HW to encourage their relatives to participate in the current study and so enhancing of the recruitment. According to the literature, the sources of information in our study are consistent. A study performed in 2008–2009 in South-Korea  with 151 HV reported word-of-mouth as the widest source of information, followed by posters or booklets in a hospital. In order to improve the recruitment of volunteers (healthy or patients), other strategies are proposed in the literature [19, 33, 36, 37]: telephone reminders to non-respondents, use of opt-out rather than opt-in procedures for contacting potential participants, newsletters/mailshots/flyers, regular visits/telephone calls, posters/information leaflets in clinics/wards/notes, or change of inclusion criteria/protocol amendment. In our study, posters and advertisements in the press and on the hospital website seemed to be moderately effective while radio and social networks did not seem very useful for recruitment. Then means and time spent for the realization of these materials should not be a priority in a strategy for recruitment.
Motivations of HV to participate in a non-financially compensated trial
The non-inclusion criterion of emergency first-aid training within the previous 12 months or rescuer status could partly explained the low rate of participations of students (15.5%) because students had often received first-aid training. Moreover, this low participation could be due to absence of financial compensation, as Van Gelderen et al.  reported that younger volunteers (18–30 years) were more likely to cite money as a reason for participation than older volunteers. Furthermore the most represented socio-professional category was employees (40.5%) Other socio-demographic factors could influenced the participation of HV in clinical trials: volunteers in a higher socioeconomic class are more likely to participate in Phase I studies  and Caucasians with a higher education level are more motivated by financial reward . One special feature of our study was absence of any financial compensation for HV. Emergency first-aid training (“learning about emergency first-aid” or “updating knowledge of emergency first-aid”) was reported to be a major motivation by most HV (85.7%). Training presented a personal benefit, probably encouraging HV participation despite absence of financial compensation, which certainly facilitated recruitment. Moreover refusal to participate due to absence of financial compensation was little reported in our study (4.6% of the 323 HV contacted by telephone who refused to participate) but under-reporting of this reason is likely, especially among those who gave no reason for refusal (38.7%). A review of the literature  showed that although financial reward is the primary motivation for HV participating in clinical trials, other motivations are reported (contributing to science or the health of others, accessing ancillary healthcare benefits, scientific interest or interest in the goals of the study, meeting people and curiosity). In our study, motivation “protocol without risk” was little reported, appearing to be a relatively low decisive criterion for participation in the trial when the risk was low. The literature shows that volunteers considered the risk when making decisions regarding participation [39, 40] and that the risk of the study was the ultimate deciding factor for the volunteers .
Satisfaction of HV
In our study, satisfaction for the overall welcome and for the protocol management was very high. A survey conducted in 2004–2005 at the CIC of Grenoble, France  also reported high satisfaction, but did not differentiate gender of participants, whereas in our study women were more satisfied than men regarding protocol management. Satisfaction is important as it improves future recruitment by the positive effect it may have on recruiting repeat volunteers, and even on recruitment of naive volunteers, especially by word-of-mouth. Indeed volunteers consider staff behaviour, their relationship with other volunteers, and other aspects of the study environment to have a large impact on their well-being while participating in the study [26, 43].
Our study has several limitations. First, telephone reachability could be a recruitment bias, indeed successful telephone contact was associated with age: older HVs were significantly more reachable than younger HVs (70.6% vs 46.1%). Second, self-reporting of measures presented a risk of classification bias. Third, satisfaction was very high and therefore analysis was a comparison of fully satisfied HV and not fully satisfied HV. This low variability criterion could result in non-identification of significant association. The interpretation of satisfaction according to socio-demographic characteristics must remain cautious, other unstudied factors could explain the difference in HV satisfaction.
The main strength of our study was the large sample size of HV recruited, despite absence of financial compensation. The recruitment of HV aged 18 to 60 years without financial compensation required broad screening with an essential updated HV database. Word-of-mouth appeared to be a more efficient source of information on the study than media advertising. One of the main motivations for participating was to benefit from a brief emergency first-aid training session at the end of the trial. Thus recruitment strategy of HV in randomized studies without financial compensation should be enhanced by providing direct interest to HV and ensuring HV satisfaction.
Ohmann C, Deimling A: Attitude towards clinical trials: results of a survey of persons interested in research.Inflamm Res Off J Eur Histamine Res Soc Al 2004,53(Suppl 2):142–147.
Agrawal M, Grady C, Fairclough DL, Meropol NJ, Maynard K, Emanuel EJ: Patients’ decision-making process regarding participation in phase I oncology research.J Clin Oncol Off J Am Soc Clin Oncol 2006, 24:4479–4484. 10.1200/JCO.2006.06.0269
Rodenhuis S, van den Heuvel WJ, Annyas AA, Koops HS, Sleijfer DT, Mulder NH: Patient motivation and informed consent in a phase I study of an anticancer agent.Eur J Cancer Clin Oncol 1984, 20:457–462. 10.1016/0277-5379(84)90229-3
Wang L-H, Tsai Y-F, Chen J-S, Tsay P-K: Intention, needs, and expectations of cancer patients participating in clinical trials.Cancer Nurs 2011, 34:117–123. 10.1097/NCC.0b013e3181efe1c0
Maloney C, Lyons KD, Li Z, Hegel M, Ahles TA, Bakitas M: Patient perspectives on participation in the ENABLE II randomized controlled trial of a concurrent oncology palliative care intervention: benefits and burdens.Palliat Med 2013, 27:375–383. 10.1177/0269216312445188
Catania C, De Pas T, Goldhirsch A, Radice D, Adamoli L, Medici M, Verri E, Marenghi C, de Braud F, Nolè F: Participation in clinical trials as viewed by the patient: understanding cultural and emotional aspects which influence choice.Oncology 2008, 74:177–187. 10.1159/000151365
Truong TH, Weeks JC, Cook EF, Joffe S: Altruism among participants in cancer clinical trials.Clin Trials Lond Engl 2011, 8:616–623. 10.1177/1740774511414444
Meneguin S, Cesar LAM: Motivation and frustration in cardiology trial participation: the patient perspective.Clin São Paulo Braz 2012, 67:603–608. 10.6061/clinics/2012(06)10
Locock L, Smith L: Personal benefit, or benefiting others? Deciding whether to take part in clinical trials.Clin Trials Lond Engl 2011, 8:85–93. 10.1177/1740774510392257
Mfutso-Bengo J, Ndebele P, Jumbe V, Mkunthi M, Masiye F, Molyneux S, Molyneux M: Why do individuals agree to enrol in clinical trials? A qualitative study of health research participation in Blantyre, Malawi.Malawi Med J J Med Assoc Malawi 2008, 20:37–41.
Carroll R, Antigua J, Taichman D, Palevsky H, Forfia P, Kawut S, Halpern SD: Motivations of patients with pulmonary arterial hypertension to participate in randomized clinical trials.Clin Trials Lond Engl 2012, 9:348–357. 10.1177/1740774512438981
Zammar G, Meister H, Shah J, Phadtare A, Cofiel L, Pietrobon R: So different, yet so similar: meta-analysis and policy modeling of willingness to participate in clinical trials among Brazilians and Indians.PLoS One 2010, 5:e14368. 10.1371/journal.pone.0014368
Udrea G, Dumitrescu B, Purcarea M, Balan I, Rezus E, Deculescu D: Patients’ perspectives and motivators to participate in clinical trials with novel therapies for rheumatoid arthritis.J Med Life 2009, 2:227–231.
Fearn P, Avenell A, McCann S, Milne AC, Maclennan G, MAVIS TRIAL GROUP: Factors influencing the participation of older people in clinical trials - data analysis from the MAVIS trial.J Nutr Health Aging 2010, 14:51–56. 10.1007/s12603-010-0009-x
Grant JB, Mackinnon AJ, Christensen H, Walker J: Participants’ perceptions of motivation, randomisation and withdrawal in a randomised controlled trial of interventions for prevention of depression.J Med Ethics 2009, 35:768–773. 10.1136/jme.2008.028035
Wasan AD, Taubenberger SP, Robinson WM: Reasons for participation in pain research: can they indicate a lack of informed consent?Pain Med Malden Mass 2009, 10:111–119. 10.1111/j.1526-4637.2008.00481.x
Newington L, Metcalfe A: Factors influencing recruitment to research: qualitative study of the experiences and perceptions of research teams.BMC Med Res Methodol 2014, 14:10. 10.1186/1471-2288-14-10
Caldwell PHY, Hamilton S, Tan A, Craig JC: Strategies for Increasing Recruitment to Randomised Controlled Trials: Systematic Review.PLoS Med 2010, 7:e1000368. 10.1371/journal.pmed.1000368
Watson JM, Torgerson DJ: Increasing recruitment to randomised trials: a review of randomised controlled trials.BMC Med Res Methodol 2006, 6:34. 10.1186/1471-2288-6-34
Lemmens T, Elliott C: Guinea pigs on the payroll: the ethics of paying research subjects.Account Res 1999, 7:3–20. 10.1080/08989629908573939
Tishler CL, Bartholomae S: The recruitment of normal healthy volunteers: a review of the literature on the use of financial incentives.J Clin Pharmacol 2002, 42:365–375. 10.1177/00912700222011409
Czarny MJ, Kass NE, Flexner C, Carson KA, Myers RK, Fuchs EJ: Payment to healthy volunteers in clinical research: the research subject’s perspective.Clin Pharmacol Ther 2010, 87:286–293. 10.1038/clpt.2009.222
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
Nappo SA, Iafrate GB, Sanchez ZM: Motives for participating in a clinical research trial: a pilot study in Brazil.BMC Public Health 2013, 13:19. 10.1186/1471-2458-13-19
Chu SH, Jeong SH, Kim EJ, Park MS, Park K, Nam M, Shim JY, Yoon YR: The views of patients and healthy volunteers on participation in clinical trials: an exploratory survey study.Contemp Clin Trials 2012, 33:611–619. 10.1016/j.cct.2012.02.018
Kass NE, Myers R, Fuchs EJ, Carson KA, Flexner C: Balancing justice and autonomy in clinical research with healthy volunteers.Clin Pharmacol Ther 2007, 82:219–227. 10.1038/sj.clpt.6100192
Russell ML, Moralejo DG, Burgess ED: Paying research subjects: participants’ perspectives.J Med Ethics 2000, 26:126–130. 10.1136/jme.26.2.126
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
Townsend A, Cox SM: Accessing health services through the back door: a qualitative interview study investigating reasons why people participate in health research in Canada.BMC Med Ethics 2013, 14:40. 10.1186/1472-6939-14-40
Grady C: Payment of clinical research subjects.J Clin Invest 2005, 115:1681–1687. 10.1172/JCI25694
Resnik DB: Limits on risks for healthy volunteers in biomedical research.Theor Med Bioeth 2012, 33:137–149. 10.1007/s11017-011-9201-1
Jones E, Liddell K: Should healthy volunteers in clinical trials be paid according to risk? Yes.BMJ 2009, 339:b4142. 10.1136/bmj.b4142
McDonald AM, Knight RC, Campbell MK, Entwistle VA, Grant AM, Cook JA, Elbourne DR, Francis D, Garcia J, Roberts I, Snowdon C: What influences recruitment to randomised controlled trials? A review of trials funded by two UK funding agencies.Trials 2006, 7:9. 10.1186/1745-6215-7-9
Lion F, Teule L, Adam C, Arrateig V, Damm C: T: Etude prospective randomisée. Etude de 3 stratégies d’assistance téléphonique à la réalisation d’un massage cardiaque continu [abstract]. XXVème colloque national des centres d’enseignement des soins d’urgence; 2013. http://ancesu.fr/Telemacc_480___341.html
Pitrou I, Dauchet L, Bailly L, Koubi SE, Tavolacci M-P, Ladner J: Mobile phone follow-up of subjects included in a prospective cohort study: unexpected difficulties.Eur J Epidemiol 2007, 22:411–412. 10.1007/s10654-007-9130-5
Treweek S, Lockhart P, Pitkethly M, Cook JA, Kjeldstrøm M, Johansen M, Taskila TK, Sullivan FM, Wilson S, Jackson C, Jones R, Mitchell E: Methods to improve recruitment to randomised controlled trials: Cochrane systematic review and meta-analysis.BMJ Open 2013, 3:e002360.
Campbell HM, Raisch DW, Sather MR, Warren SR, Segal AR: A comparison of veteran and nonveteran motivations and reasons for participating in clinical trials.Mil Med 2007, 172:27–30.
Van Gelderen CE, Savelkoul TJ, van Dokkum W, Meulenbelt J: Motives and perception of healthy volunteers who participate in experiments.Eur J Clin Pharmacol 1993, 45:15–21. 10.1007/BF00315344
Bigorra J, Baños JE: Weight of financial reward in the decision by medical students and experienced healthy volunteers to participate in clinical trials.Eur J Clin Pharmacol 1990, 38:443–446. 10.1007/BF02336681
Breitkopf CR, Loza M, Vincent K, Moench T, Stanberry LR, Rosenthal SL: Perceptions of reimbursement for clinical trial participation.J Empir Res Hum Res Ethics JERHRE 2011, 6:31–38.
Hassar M, Pocelinko R, Weintraub M, Nelson D, Thomas G, Lasagna L: Free-living volunteer’s motivations and attitudes toward pharmacologic studies in man.Clin Pharmacol Ther 1977, 21:515–519.
Paris A, Bosson J-L, Melis MS, Moreau-Gaudry A, Hommel M, Cracowski J-L: Evolution of the satisfaction of subjects enrolled in clinical studies.Therapie 2006, 61:419–423. 10.2515/therapie:2006073
Hermann R, Heger-Mahn D, Mahler M, Seibert-Grafe M, Klipping C, Breithaupt-Grögler K, de Mey C: Adverse events and discomfort in studies on healthy subjects: the volunteer’s perspective. A survey conducted by the German Association for Applied Human Pharmacology.Eur J Clin Pharmacol 1997, 53:207–214. 10.1007/s002280050364
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2288/15/2/prepub
We are grateful to Nikki Sabourin-Gibbs, Rouen University Hospital, for writing assistance and reviewing the manuscript in English.
The authors declare no funding.
The authors declare that they have no competing interests.
MPT conceived the study, and participated in its design and coordination. CaD, QL, CeD, LP and FL participated in data acquisition and QL performed data extraction. QL performed statistical analysis. QL and MPT performed interpretation of data. QL drafted the manuscript and MPT helped to draft the manuscript. All authors contributed to critical revision and have read and approved the final manuscript.