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SUPPLEMENT |
1 Centre for Behavioural Research and Program Evaluation, University of Waterloo, Waterloo, Ontario, Canada
2 University of Rochester Medical Center, Rochester New York, USA
3 North American Quitline Consortium, Phoenix, Arizona, USA
4 ClearWay Minnesota, Minneapolis, USA
Correspondence to:
H Sharon Campbell, Evaluation Studies, Centre for Behavioural Research and Program Evaluation, Lyle Hallman North, University of Waterloo, Waterloo, Ontario, Canada, N2L 3G1; sharoncm{at}healthy.uwaterloo.ca
Received 2 January 2007
Accepted 23 July 2007
| ABSTRACT |
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Methods: The North American Quitline Consortium (NAQC) assembled a working group with representatives from quitline service providers, funders, evaluators and researchers from Canada and the United States. An extensive, iterative consultation process over two years led to consensus on the evaluation domains, indicators and specific items. Descriptive information on quitline service models, data collection protocols and methodological issues were addressed.
Results: The resulting minimal dataset (MDS) includes 15 items collected from eligible callers at intake and eight items collected from smokers participating in evaluation. Recommendations for selecting evaluation participants, length of follow-up and repeat callers were developed. Full MDS questions and technical documents are available on the NAQC website.
Conclusion: Adoption and implementation of the MDS occurred in the majority of North American quitlines by the end of 2006. Key success factors included a focus on utility and feasibility, a commitment to meeting multiple and varied needs, sensitivity to situational factors and investment in working interactively with stakeholders. The creation and implementation of a MDS across two countries is an important "first" in tobacco control which will help speed the creation of practice based evidence and facilitate practice based research.
Abbreviations: ENQ, European Network of Quitlines; ESCHER, European Smoking Cessation Helplines Evaluation Research; MDS, minimal dataset; NAQC, North American Quitline Consortium; SRNT, Society For Research On Nicotine And Tobacco
Keywords: quitlines; evaluation; research; tobacco; cessation
To achieve meaningful and rapid reductions in tobacco related morbidity and mortality, we must increase both the number of individuals who attempt to quit, and the success rate of those attempts. Among the many available cessation programmes, telephone based cessation services, also known as quitlines, offer the opportunity to achieve both goals because of their broad reach and effectiveness.1–5 Two Cochrane reviews have supported quitlines, particularly those that offer proactive services, as an effective population based approach to tobacco cessation.1 2 Studies have also shown quitlines to be cost effective6 and cost beneficial.7 In fact, quitlines are increasingly being recognised as a key component of comprehensive tobacco control strategies in Australia,8 Canada, the United Kingdom, the United States9 10 and the European Union.
The emergence of quitlines as a population based approach to smoking cessation has followed the classic innovation diffusion curve,11 at least in North America. The first North American quitline service at a population level began in California in 1992; by 2002 there were 33 state and provincial quitlines and by 2006 all smokers in North America had access to quitline services.12 Despite the proliferation of quitlines there were no agreed upon metrics or standards for evaluation, making it difficult for quitlines to learn from each other, and comparative studies impossible.
The first North American Conference of Smoking Cessation Quitlines was held in Arizona in 2002. Participants at that meeting asked for a common approach to evaluation. The North American Quitline Consortium (NAQC), which was established two years later to provide leadership and a unified voice for quitlines, led the initiative to create a common evaluation approach. This paper describes the development of an evaluation framework and standardised set of measures (now known as the minimal dataset or MDS) designed to inform quitline operations, facilitate comparative evaluation studies and enhance research opportunities.
| EVALUATION FRAMEWORK |
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This framework and accompanying principles were especially relevant for the creation of a common dataset for evaluating quitlines. There were a large and diverse number of stakeholders with an interest and enthusiasm for learning what works in what settings and for whom. The rich diversity of quitline service delivery models, clients and target populations in different settings across North America made comparative studies possible via the adoption of a set of common measures.
| DEVELOPMENT PROCESS |
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The process, illustrated in table 1, occurred over two years. The working group operated via teleconference and email, with key face to face meetings attached to other meetings and conferences, all supported by funding from NAQC sponsors, Health Canada and the Canadian Tobacco Control Research Initiative. Members of the working group provided leadership and momentum for the MDS, both internationally and within their own organisations. In addition, researchers with the European Smoking Cessation Helplines Evaluation Research (ESCHER) group of the European Network of Quitlines (ENQ) participated in key meetings.
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The Working Group adopted a set of guiding principles to ensure the MDS would facilitate service provision, evaluation and research, make comparisons possible and not impose undue resource burdens on quitlines. These principles were operationalised as follows:
After decisions on evaluation domains and question wording were approved, the working group addressed protocols for data collection, issues pertaining to length of follow-up, repeat callers and information needed to understand the uniqueness of each quitline.
The final MDS and protocols were approved by the Research and Evaluation Working Group in February 2005. To facilitate implementation, NAQC shared the MDS with all NAQC members and interested parties by email, on the NAQC website and during the first NAQC annual meeting in May 2005. NAQC also hired a technical expert and offered assistance via conference calls, online resources and individual consultation for a six-month period.
By the end of 2005, all quitlines reported that voluntary implementation of the MDS was planned or under way. A NAQC survey of MDS implementation is planned for 2007 to determine implementation, fidelity, areas for update and new information needs.
| MINIMAL DATASET |
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Three factors that have consistently been shown to predict quit success (nicotine dependence, readiness to quit, use of other quit aids) are also captured. Although many quitlines use stages of change to inform their counselling interventions, the working group did not include it in the MDS given the equivocal evidence of its predictive validity for quit success when other factors are taken into account.14–16
Table 2 outlines the MDS intake and follow-up questions, the corresponding evaluation indicators and examples of the types of decisions informed by each domain. The MDS questions and technical documents are posted on the NAQC website at www.naquitline.org/index.asp?dbid = 2&dbsection = research.
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There is also considerable variability in quitlines evaluation mandates and resources. With respect to evaluation methodology, the working group concluded: "Each quitline will need to determine how follow-up will be conducted and on which population. ...[quitlines] should strive to survey enough people to draw valid conclusions about their outcomes, but it will be up to the individual quitline to determine whether census surveying, random sampling, cohort sampling, or some other sampling method will be most appropriate."17 While not ideal from a research perspective, this approach made implementation of the MDS possible with the expectation that in future common evaluation methodologies could also be implemented.
The working group followed expert guidelines for abstinence measures,19 20 recommending at minimum, six-month follow-up and 30-day point prevalence. This measure was meaningful to funders and follow-up was feasible for quitlines. Quitlines already measuring prolonged abstinence and 12-month outcomes were encouraged to continue. NAQC also recommended that quitlines report abstinence rates using both an "intent to treat" analysis and analysis of only those who completed the evaluation, with the recognition that the true quit rate lies somewhere between the two measures. It was also determined that a one-month intervention period would permit completion of most or all proactive counselling calls for most quitlines. Thus the working group recommended the follow-up interviews occur seven months after the intake date. This allowed one month for the full intervention (or at least the majority of proactive calls), plus the standard six-month follow-up period.
The final issue tackled by the working group was how to treat repeat callers. A small percentage of callers make extensive use of quitlines and the dilemma was at what point to consider them as making a new quit attempt versus continuing to act on the original counselling intervention. After considerable debate, it was agreed that a 12-month period from the first quitline contact should be considered a new quit attempt. Thus smokers who relapsed but called back for a second quit attempt 13 or more months after their original call to the quitline would be considered as new callers for evaluation purposes.
| DISCUSSION |
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A desire to keep the MDS small and operationally feasible took paramount importance in discussions. It was recognised that the MDS must be easy to implement and be respectful of quitlines service mandate. The multi-stakeholder working group enabled satisfactory resolution between researchers desire for comprehensive baseline data and service providers concerns about the time required to collect those data. As one participant noted "What made this work was willingness on the part of the researchers to balance scientific rigor with practicality, coupled with a respect for and interest in scientific integrity on the part of program and policy decision makers."
A second key success factor was accommodating differences across quitlines. Individual quitlines each had their own evaluation questions to preserve and reasons for wanting to do so. Acknowledgement that the MDS was an adjustment to existing protocols authenticated individual quitline evaluation processes while at the same time moved the field as a whole toward a core set of items. The resulting MDS replaced some but not all pre-existing questions.
Though time intensive, the multi-stakeholder collaborative approach was another key success factor. As noted by one quitline service provider, "The collaborative approach was unique and progressive. By bringing together such a range of stakeholders, all perspectives were represented from the very beginning, which allowed informed and rapid input, critiquing and feedback to produce a MDS that will be relevant and manageable to implement". Also important to success was the momentum, started by Ossip-Klein in a presentation at the North American Conference of Smoking Cessation Quitlines and continued by the co-chairs and members of the working group. Finally, NAQCs role in communicating and providing technical assistance to address implementation issues and support quitlines was critical.
There are several early indicators of the success of this endeavour. As of December 2006, the majority of US states and almost all Canadian provinces are implementing the MDS at some level (Bailey, personal communication). Other indicators of success include adoption of the MDS as a template for data collection by the University of Massachusetts Tobacco Treatment Specialist Training Program. The US Centers for Disease Control and Prevention asked quitlines they fund to report on the use of the MDS.9 Other institutions have recognised the value of standardised data and are proposing to adapt the MDS or create a similar standardised dataset (Web Assisted Tobacco Intervention Initiative; University of Rochester Medical Center; the Ontario Tobacco Research Unit; and the Association for the Treatment of Tobacco Use and Dependence).
| CONCLUSION |
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What this paper adds
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| ACKNOWLEDGMENTS |
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Erik Augustson, Tobacco Control Research Branch, National Cancer Institute; Linda Bailey (Co-Chair MDS Working Group), North American Quitline Consortium; Sharon Campbell (Co-Chair MDS and R&E Working Groups), Centre for Behavioural Research and Program Evaluation, University of Waterloo; Sharon Cummins, California Smokers Helpline, University of California San Diego; Donna Czukar, Cancer Information and Support, Canadian Cancer Society; Corinne Husten, Office on Smoking and Health, Centers for Disease Control and Prevention; Ann Malarcher, Office on Smoking and Health, Centers for Disease Control and Prevention; Paul McDonald, Population Health Research Group, University of Waterloo; Deborah Ossip-Klein (Co-Chair R&E Working Group), Smoking Research Program, University of Rochester; Joanne Pike, American Cancer Society; Abby Rosenthal, Office on Smoking and Health, Centers for Disease Control and Prevention; Barbara Schillo, ClearWay Minnesota; Donna Vallone, Research and Evaluation, American Legacy Foundation; Susan Zbikowski, Clinical and Behavioral Sciences, Free & Clear, Inc.
| REFERENCES |
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This article has been cited by other articles:
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L. M Hayward, H S. Campbell, and C. Sutherland-Brown Aboriginal users of Canadian quitlines: an exploratory analysis Tob. Control, December 1, 2007; 16(Suppl_1): i60 - i64. [Abstract] [Full Text] [PDF] |
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