- Research article
- Open Access
Mail merge can be used to create personalized questionnaires in complex surveys
© Taljaard et al. 2015
Received: 6 February 2015
Accepted: 7 October 2015
Published: 16 October 2015
Low response rates and inadequate question comprehension threaten the validity of survey results. We describe a simple procedure to implement personalized—as opposed to generically worded—questionnaires in the context of a complex web-based survey of corresponding authors of a random sample of 300 published cluster randomized trials. The purpose of the survey was to gather more detailed information about informed consent procedures used in the trial, over and above basic information provided in the trial report. We describe our approach—which allowed extensive personalization without the need for specialized computer technology—and discuss its potential application in similar settings.
The mail merge feature of standard word processing software was used to generate unique, personalized questionnaires for each author by incorporating specific information from the article, including naming the randomization unit (e.g., family practice, school, worksite), and identifying specific individuals who may have been considered research participants at the cluster level (family doctors, teachers, employers) and individual level (patients, students, employees) in questions regarding informed consent procedures in the trial. The response rate was relatively high (64 %, 182/285) and did not vary significantly by author, publication, or study characteristics. The refusal rate was low (7 %).
While controlled studies are required to examine the specific effects of our approach on comprehension, quality of responses, and response rates, we showed how mail merge can be used as a simple but useful tool to add personalized fields to complex survey questionnaires, or to request additional information required from study authors. One potential application is in eliciting specific information about published articles from study authors when conducting systematic reviews and meta-analyses.
The design of clear and comprehensible questionnaires is essential in promoting survey validity, but this can be challenging when the subject matter is complex and the target population heterogeneous. Ambiguous wording may decrease response and item completion rates due to perceived difficulty of questions and respondent frustration or fatigue; it can also increase measurement error due to poor question comprehension. As part of a larger study examining ethical issues in cluster randomized trials [1, 2], we reviewed a random sample of 300 cluster randomized trials in health research published between 2000 and 2008 . Due to the paucity of specific information about ethical issues reported in the sample of trials , we designed a survey to gather more detailed information from the corresponding authors. The survey was complex: it aimed to gather specific information about the presence of any cluster “gatekeepers” or other individuals who were approached for permission to randomize clusters, as well as informed consent procedures administered to research participants at the cluster and/or individual level. Further details and results of the survey may be found elsewhere [5, 6]. We were faced with several challenges in designing our questionnaire, including diversity of the sample with respect to country and research area of study authors, potential lack of familiarity with the concept of cluster randomization, lack of standard definitions of “gatekeepers” and “research participants”, and diversity of key elements of the trials themselves including types of clusters (e.g., medical practices, schools, communities, work sites, sports teams), types of participants at the individual level and/or cluster level, and specific study interventions and data collection procedures that may or may not have required consent. These challenges made a traditional survey that presented questions in a uniform way problematic to operationalize.
To address these challenges, we considered using an interviewer-administered telephone survey, which would allow real-time clarifications to respondents. However, this was considered logistically infeasible given the sample size. A self-administered web-based questionnaire with the addition of a glossary of definitions was a second option, but would have considerably increased the length of the questionnaire without necessarily improving question comprehension. A third and preferred option was to generate a unique, personalized questionnaire for each sample member. This would allow us to customize the questions to each author by incorporating study-specific information from the published article, including naming the randomization unit or “cluster” (e.g., family practice, school, worksite, sports team), and referring to specific individuals who might be considered potential participants at the cluster level (e.g., health care providers, teachers, employers, coaches) and individual level (e.g., patients, students, employees, players). We expected that this would not only improve question comprehension leading to higher quality results, but also increase participation as the incorporation of personal information might increase saliency . While telephone, face-to-face and web-based questionnaire customization has been used for decades at survey organizations, supported by advances in computer-assisted interviewing [8, 9], we were restricted to the use of a simple and cheap self-administered method that did not require specialized computer technology.
Examples of items personalized in our survey questionnaire showing extent of personalization required to generate n = 285 unique questionnaires
Type of information
Personalized wording (based on target study publication)
Total number of unique fields
Study title, journal, and year of publication
Your study was randomly selected for this survey
Your study (A Cluster-Randomized Controlled Trial Evaluating the Effect of a Handwashing-Promotion Program in Chinese Primary Schools,) published in [Am J Trop Med Hyg (2007)] was randomly selected for this survey
Research ethics approval
Did you seek ethics approval to conduct the study?
[Our review of your paper indicates that research ethics approval was (sought) (not sought) to conduct the study. Is this correct?]
Type of committee
How many ethics committees did you approach?
How many [institutional review boards (IRBs)] [Research Ethics Boards (REBs)] [Research Ethics Committees (RECs)…] did you approach?
Did one or more gatekeepers provide agreement or consent to the clusters’ involvement in your study?
Did any (school principals or school district administrators) provide agreement or consent to the involvement of (schools) in your study?
Any other permission
Did you seek approval from anyone else to conduct the study?
Did you seek approval from anyone else, such as: (Ministry of Education, Department of Public Health, or school advisory board,) to conduct the study?
Unit of randomization
Was consent sought before randomization of clusters?
Was consent sought before randomization of (schools)?
Cluster level participants
Did cluster-level participants in the intervention arm provide consent?
Did (the teachers) in your intervention arm consent to receiving the study interventions?
Individual level participants
Did individual level participants provide consent?
Did (parents or guardians of students) consent to the collection of data in your study?
We used cognitive interviewing [7, 10] to identify troublesome terms in the initial generic version, and to pre-test the personalized version. Participants for cognitive interviewing were primary authors of published cluster randomized trials, selected to represent a range of countries, types of interventions, and study settings. Fifteen individuals were invited to participate in a 45–60 min session and 11 agreed. Immediately prior to the session, we emailed the survey cover letter and a Word version of the questionnaire formatted as a fillable form. Participants were asked not to view the documents until the start of the session. As they completed the questionnaire, participants were asked to verbalize their thoughts and actions, from reading the questions aloud, to providing their final answers. Participants were also asked to share their overall impression of the questionnaire and survey. Following each interview, the survey questionnaire was modified iteratively to reflect any new understanding that had arisen. Comments from earlier think-aloud sessions that the questionnaire is, for example, “complicated to work through and read” contrasted with comments from later think-aloud sessions that the questionnaire is, for example, “nicely laid-out, easy to go through.”
The final questionnaire was operationalized into a secure web survey using MS Visual Studio 2005 and MS SQL Server 2000. Upon each successful login attempt, respondents were time-stamped in the survey database. Open text boxes were placed throughout so that respondents could clarify a response, or provide a written explanation. The web-based interface was tested on multiple platforms prior to full-scale implementation. The estimated final questionnaire completion time was 15–20 min. A pre-notification email was sent followed shortly by the survey invitation containing the survey URL, the title of the published study, unique password, and details of the survey incentive (a book on the design and analysis of cluster randomized trials). One week later, a thank you and reminder email was sent. Non-respondents were emailed a reminder 2 weeks after the initial survey invitation, and thereafter were mailed a reminder letter by post. The response rate was calculated according to the American Association for Public Opinion Research (AAPOR) guideline for web surveys of specifically named persons . We tabulated response rates by author, publication, and study characteristics thought to be associated with an increased risk of nonresponse, and tested the statistical significance of differences using Chi squared or Wilcoxon two-sample tests.
Results and discussion
Response rates to surveys are generally declining, particularly among healthcare practitioners. While questionnaire personalization has been used for many years in survey research, and experimental effects of computerization and instrument customization on survey outcomes has been studied using more rigorous research designs (e.g., [12–14]), web-based questionnaires are still scarce in Epidemiological research , and we are unaware of previous studies that have used simple mail merge to customize a complex survey questionnaire within the setting of a systematic review. We examined the potential impact of our approach by considering feedback from participants, the survey response rate, implicit and explicit refusal, and variability of response rates across publication, study, and author characteristics. We expected that questionnaire personalization might facilitate questionnaire comprehension, reduce potential points of frustration, and reduce barriers to response and completion: although we were unable to rigorously evaluate its impact within the scope of our study, we received no negative feedback and only two requests for clarification from participants despite the high degree of complexity of the survey topic and diversity of the sample. Although the survey was relatively long, the response rate was 64 %—higher than the average response rate of 58 % found in a review of surveys of health professionals . Given that this was an international survey of busy researchers, whose studies may have been published several years earlier and whose first language may not have been English, this response rate was considered acceptable. Response rates were similar across countries of the primary author as well as various publication and study characteristics.
While we believe that personalization was a factor in our successful response rate, we were unable to use experimental manipulation to examine its effects more rigorously. In particular, we lacked a control group that presented respondents with the alternative generic question language and therefore cannot attribute our success solely to this aspect of our survey. It is possible that other features of the survey, including the personalized invitations and the composition of our study population (researchers and scientists) facilitated questionnaire completion. Our results, therefore, are merely descriptive; future work should involve stronger designs to determine the effect of questionnaire personalization on survey response and measurement error, and in different populations. Nevertheless, Table 1 provides an indication of the extent of personalization required in our survey: without the provision of these study-specific terms, respondents would have been required to make the conversions from the generic term to the study-specific term with substantially increased risk of error and misunderstanding.
We believe that our simple approach to questionnaire personalization may be useful in other settings where resource constraints limit access to more sophisticated technology, where surveyors have access to prior information about sample members or where a sample is diverse and terminology differs across settings. For example, when conducting systematic reviews and meta-analyses of original research studies , inadequate reporting of study procedures and outcomes in publications often necessitates contacting study authors to obtain missing information. Contacting study authors is encouraged because syntheses of incomplete data can lead to biased estimates [18, 19]. A common method is email solicitation, where data collection forms are sent by email attachment. To promote higher response rates and improve response accuracy, researchers may consider the use of the mail merge feature to add personalized fields to data collection forms. Future research studies could consider the use of experimentation to rigorously examine the effects of this approach and to explore improved comprehension versus saliency as plausible pathways to improved response.
MT contributed to the study design, supervised the analyses, and drafted the manuscript. SHC contributed to the study design, coordinated and implemented the study, carried out the analyses, and contributed to the drafting of the manuscript. JCB, CW, and JMG contributed to the study design, implementation of the study and drafting of the manuscript. All authors read and approved the final manuscript.
This work was supported by the Canadian Institutes of Health Research [grant number MOP85066, MOP89790]. Jeremy Grimshaw holds a Canada Research Chair in Health Knowledge Transfer and Uptake. Charles Weijer holds a Canada Research Chair in Bioethics. The web survey was designed by senior programmer Dong Vo at the Methods Centre of the Ottawa Hospital Research Institute (OHRI). We thank the authors of the sample of trials for taking the time to complete our survey questionnaire.
The authors declare that they have no competing interests.
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