Introduction Patient decision aids (PDAs) have been developed to help patients make an informed choice for a treatment option. Despite proven benefits, structural implementation falls short of expectations. The present study aims to assess the effectiveness and cost-utility of the PDA among newly diagnosed patients with localised prostate cancer and their partners, alongside implementation of the PDA in routine care.
Methods/analysis A stepped-wedge cluster randomised trial will be conducted. The PDA will be sequentially implemented in 18 hospitals in the Netherlands, over a period of 24 months. Every 3 or 6 months, a new cluster of hospitals will switch from usual care to care including a PDA.
The primary outcome measure is decisional conflict experienced by the patient. Secondary outcomes comprise the patient’s quality of life, treatment preferences, role in the decision making, expectations of treatment, knowledge, need for supportive care and decision regret. Furthermore, societal cost-utility will be valued. Other outcome measures considered are the partner’s treatment preferences, experienced participation to decision making, quality of life, communication between patient, partner and health care professional, and the effect of prostate cancer on the relationship, social contacts and their role as caregiver. Patients and partners receiving the PDA will also be asked about their satisfaction with the PDA.
Baseline assessment takes place after the treatment choice and before the start of a treatment, with follow-up assessments at 3, 6 and 12 months following the end of treatment or the day after deciding on active surveillance. Outcome measures on implementation include the implementation rate (defined as the proportion of all eligible patients who will receive a PDA) and a questionnaire for health care professionals on determinants of implementing an innovation.
Ethics and dissemination This study will be conducted in accordance with local laws and regulations of the Medical Ethics Committee of VU University Medical Center, Amsterdam, The Netherlands. The results from this stepped-wedge trial will be presented at scientific meetings and published in peer-reviewed journals.
Trial registration Nederlands Trial Register NTR TC5177, registration date: May 28th 2015.Pre-results.
- Shared decision making
- decision aid
- prostate cancer
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Strengths and limitations of this study
With a stepped-wedge cluster randomised trial, we aim to evaluate the effectiveness and cost-utility in clinical care for patients with prostate cancer while simultaneously and sequentially implementing an intervention (the patient decision aid). The expectation is that this approach will lead to sustainable implementation of the patient decision aid.
Because the majority of patients with prostate cancer (as well as partners themselves) have the opinion that their partner has played a major role in the treatment decision, we also involved the partners of patients with prostate cancer in this study.
Disadvantage of the stepped-wedge cluster randomised trial is the extended study duration due to sequential intervention rollout and the complicated analysis due to the unidirectional crossover.
Prostate cancer is the most common form of cancer in men over 55 years in the Netherlands. The vast majority of these men have a localised form of prostate cancer, meaning that the cancer is only present in the prostate gland and has not spread to another part of the body.1 For the initial treatment of localised prostate cancer, there are multiple, medically equivalent curative treatment options (radical prostatectomy, external beam radiotherapy or brachytherapy) as well as the option not to be treated immediately by following an active surveillance (AS) protocol. Each of these approaches has its own side effects, risks and possible consequences for the patient and his partner.2–4 Currently, patients are informed about the treatment options, with often a well-intentioned preference by the healthcare professional (HCP).5 6 As long as none of these treatment options has proven to be superior,7 a patient should be able to make a decision based on his own preferences and values such as maintaining sexual function and urinary continence.8
Patient decision aids (PDAs) are tools, which can be used to help patients make specific and informed choices among options by providing information on the outcomes relevant to a person’s health status.9 Multiple studies showed that PDAs improve patients’ knowledge, participation in decision making and support patients to reach choices that are more consistent with their informed values.8 10–12
Usually, PDAs are developed and consequently evaluated in randomised controlled trials investigating effectiveness. Despite proven benefits of PDAs, structural implementation falls short of expectations. Barriers for implementation were recently revealed in reviews13 14: HCPs do not trust the content of PDAs, they question if the information provided is evidence-based or they think that the PDA does not reflect ‘local’ data.13 Time pressure, lack of applicability due to patient characteristics (eg, patients’ literacy levels) and limitations due to clinical factors (eg, if a patient is not eligible for more than one option) were other barriers mentioned by HCPs.14 To overcome these hurdles, we developed a PDA for patients with localised prostate cancer and prepared an overview of requirements for implementation using an iterative participatory approach, meaning that patients with prostate cancer and HCPs were involved in each step of the development process.15–17 This approach resulted in a PDA that fits the needs of patients and HCPs with the aim to ensure adequate uptake in daily clinical practice. See the Methods section for more information on the PDA and its development process.
The present study aims to assess the effectiveness and cost-utility of the PDA among newly diagnosed patients with localised prostate cancer and their partners, alongside implementation of the PDA in routine care via a stepped-wedge clustered randomised controlled trial. To our knowledge, there are no stepped-wedge cluster randomised trials with PDAs for patients with prostate cancer that evaluate both the effectiveness, cost-utility and implementation of a PDA.
Based on the Cochrane study of Stacey et al,8 we hypothesise that the PDA will improve knowledge on prostate cancer, satisfaction with the information provided and prepare patients for the treatment choice and can thus lead to a reduction in Decisional Conflict Scale (DCS). Moreover, we expect the PDA to make patients more aware of the choice and can thus lead to a change in the role patients want to have in the decision-making process (eg, be more active).8 Additionally, we hypothesise that the PDA will also result in more realistic expectations of the treatment and to less regret afterwards.18 19
Because studies have shown that the majority of patients with prostate cancer (as well as partners themselves) have the opinion that their partner has played a major role in the treatment decision,20 21 we will evaluate the effect of a PDA on partners as well.
A prospective stepped-wedge cluster randomised controlled trial will be conducted to compare the PDA with usual care.22 We followed the SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) checklist23 24 (see appendix A). A stepped-wedge cluster randomised controlled trial is a research design in which a new treatment is sequentially implemented in a set of clusters (see figure 1). A stepped-wedge design is applied to assure implementation of the PDA in all of the participating hospitals while still allowing for a comparison with usual care. The order in which the clusters start with the new intervention is randomised. Until the time of implementation of the new intervention, clusters serve as a control group. A flowchart of the trial is shown in figure 2.
Newly diagnosed patients with prostate cancer and their partners from the participating centres between 2014 and 2016 (see figure 2) are asked to participate in the study.
Newly diagnosed patients with localised prostate cancer (and their partners) who have to choose a curable treatment option (radical prostatectomy, external beam radiotherapy or brachytherapy) for prostate cancer and have not undergone this treatment yet or have the option not to be treated immediately by following an AS protocol.
Patients diagnosed with prostate cancer TNM classification: T4, N1, M1, patients younger than 18 years or patients not able to understand the Dutch language in speech and in writing.
The inclusion and exclusion criteria are limited in order to remain close to daily clinical practice.
At the time of development, there was no PDA available in Dutch covering all four treatment options, including AS. Therefore, we developed a web-based and booklet version of a PDA for patients with localised prostate cancer.25 Figure 3 provides an overview of the followed steps in the development process. A qualitative assessment of needs among patients (n=12) recently treated for localised prostate cancer, their partners (n=4) and HCPs (n=10) by means of three focus group interviews was conducted (step 1).25 HCPs considered medical information on treatments and side effects as most important to be included in the PDA. Patients also focused on non-medical considerations. Both patients and HCPs expected the PDA to support patients in making a treatment choice. Based on the results of the focus groups, a prototype of the PDA was developed. In step 2, the prototype was presented to patients with prostate cancer (n=14) and HCPs (six urologists, four radiation therapists and three oncology nurses) in semistructured interviews. With these interviews, we also gained insight into requirements for implementing the PDA among HCPs.25 According to HCPs incorporation of the PDA into clinical guidelines and using the guidelines as a basis for the PDA would promote implementation. Finally, in step 3, the usability of the PDA was tested in a usability study among newly diagnosed patients (n=5) with localised prostate cancer targeting system quality (ease-of-use), content quality (usefulness and relevance) and service quality (the process of care provided).25–27 Usability tests showed that patients managed to ‘navigate through’ the PDA independently.25
However, some weaknesses were identified in the above-mentioned studies by HCps and patients, for example, using jargon.25 Based on these findings, the prototype of the PDA was finalised. An example of an adjustment was the addition of a glossary.
The PDA (see figure 4) includes all options for localised prostate cancer and is composed of the following parts:
A general explanation with information about the content of the PDA. It also explains that patients have multiple (treatment) options and that the choice can be made in consultation with the HCP (see figure 4a).
A section that describes all (treatment) options in short terms. The HCP can mark which (treatment) options are open for patients, if not all options are possible (see figure 4b).
A component that answers the question: what are my arguments for and against different (treatment) options for my prostate cancer? All four (treatment) options are discussed separately. All the pros and cons are described and divided into three subcomponents: cure, treatment and quality of life (see figure 4c). All statements are presented in a clear manner from the patient’s perspective (‘As long as I am under active surveillance, I will not have any side effects’). The PDA does not include ranking of features of (treatment) options or a (treatment) advice but aids the patient to reach an informed treatment preference.
A glossary of the terminology. Because of the difficulty of some terms, it was decided to include a glossary that defines all difficult terms in alphabetical order. To be comprehensible for patients low on health literacy, the content was adjusted to an intermediate preparatory vocational education level (see figure 4d).
Study design and procedures
The PDA will be stepwise implemented in 18 hospitals (five groups of two or four hospitals) in the region of Amsterdam, The Netherlands, over a period of 24 months (2014–2016).
Every 3 or 6 months (starting in 2014), a subgroup of hospitals will switch from usual care to use of the PDA (see figure 1). In each hospital, there will be a period of 4–16 months of including newly diagnosed patients who receive usual care, followed by a period of at least 5 months and a maximum of 20 months in which the PDA is provided to newly diagnosed patients. The assignment of hospitals to groups switching at different times to use of the PDA is randomised by PMvdV. The only restriction on the randomisation is that both university hospitals will not be not assigned to the same group.
Participating centres know in advance when they will implement the PDA but will not receive the PDA before the start of the implementation. HCPs (urologists and oncology nurses) partaking in this study will be trained on how to introduce the PDA to eligible patients by means of a kick-off meeting organised in their hospital shortly before the start of the implementation of the PDA.
Patients (and their partners) receive a letter from their HCP with information on the study and an invitation to participate. Patients in the intervention condition will also receive the PDA. Depending on the local healthcare pathway for patients with localised prostate cancer, the PDA will be introduced by the HCP at diagnosis or during consultation following diagnosis. Next to the PDA, patients will receive all information (eg, brochures) that would also have been provided otherwise. Patients are offered the web-based version or the booklet version of the PDA (or both), depending on the preference of the patient. In case the patient is interested in participating, the researcher informs the patient on the study in more detail by telephone and invites the patient to participate in the study. In case the patient has a partner, the partner is also invited to participate. When the patient (and partner) agrees to participate (irrespective of the participation of a partner), the researcher sends the baseline questionnaire and an informed consent form (see figure 2).
The primary outcome measure is decisional conflict (DCS) in patients (table 1). Secondary outcomes are quality of life, treatment preferences, role in the decision-making process, expectations of treatment, knowledge, communication between patient and partner, need for supportive care, decision regret and satisfaction with the PDA. Furthermore, cost-utility will be evaluated. Regarding the partners, their primary outcome measures are treatment preferences and the experienced participation and approach to decision making. Secondary outcome measures for partners include quality of life of partners, and the effect of prostate cancer on the relationship, communication between patient, partner and HCPs, social contacts and support and their role as caregiver and satisfaction with the intervention.
Participants can choose to complete the questionnaires online or by using a paper questionnaire. Non-respondents will be contacted by telephone within 2 weeks. If they do not respond to this reminder, they will be sent a reminder letter within 2 weeks.
The primary outcome (DCS), treatment preferences, preferred role in treatment decision, expectations of the treatment, knowledge and satisfaction with the intervention are collected at baseline (T0, directly after making the decision and before start of treatment). Other outcome measures are collected at baseline, after 3, 6 and 12 months follow-up. Follow-up starts on completion of treatment. Completion of treatment is defined as the last day after irradiation in case of brachytherapy or external beam radiation therapy or the day after the removal of the catheter in case of surgery, or the day after deciding on AS. An overview of the patient reported outcome measures is presented in table 1. The follow-up will end in June 2017.
Outcome measures on implementation include the implementation rate and a questionnaire for HCPs on determinants important for implementing an innovation based on the Measurement Instrument for Determinants of Innovations (MIDI) tool, which identifies barriers and facilitators at the level of the innovation (the PDA itself), the user (HCP) and the organisation (hospital).
Primary outcome measure patients
The DCS measures personal perceptions of uncertainty in choosing options, modifiable factors contributing to uncertainty such as feeling uninformed, unclear about personal values and unsupported in decision making and effective decision making such as feeling the choice is informed, values-based, likely to be implemented and expressing satisfaction with the choice. Items are given a score of 0=strongly agree, 1=agree, 2=neither agree nor disagree, 3=disagree and 4=strongly disagree. The 16 items are summed, divided by 16 and multiplied by 25. Scores range from 0 (no decisional conflict) to 100 (extremely high decisional conflict).28
Secondary outcome measures patients
With a study specific questionnaire, information regarding the preferred treatment option is obtained retrospectively. The four-item questionnaire contains questions about which of the four (treatment) options are open for the patient, which preference the patient had directly after diagnosis (retrospectively) and which preference patient has today. In addition, the degree of preference is asked.
Preferred roles in treatment decision making
For the degree of different roles in decision-making involvement, a study-specific questionnaire based on the Deber-Kraetschmer Problem-Solving Decision-Making Scale (four items) supplemented with study specific questions (two items), will be used to examine the role patients want to play in treatment decision making and the relation with the information received. In addition, the influence of the HCP and the partner on the choice made by the patient is added to this questionnaire (three additional items).29
Expectations of treatment
To assess the expectations for each of the possible treatments, the Stanford Expectations of Treatment Scale (SETS) is used. The six-item SETS is an instrument for measuring positive and negative treatment expectancies and contains two subscales: positive expectancy and negative expectancy. Positive expectancy is the average of items 1, 3 and 5. Negative expectancy is the average of items 2, 4 and 6. Questions 7–10 are not scored and just provide optional information.30
Knowledge about prostate cancer
Knowledge about prostate cancer is assessed by means of a study-specific subjective and objective questionnaire based on questionnaires on Decision Quality Instrument (DQI) knowledge and PCA 0915 and contains five objective items and four subjective items.31 32
Communication between patient and partner
Using a study-specific questionnaire based on the study of Zeliadt, patients and their partners will be asked about their communication with each other about prostate cancer.21
The need for supportive care (including prostate specific part)
The Supportive Care Needs Survey (SCNS) SF-34 is an instrument for the assessment of the perceived needs for aftercare of people diagnosed with cancer. The questionnaire contains a total of 34 items, with the following five domains: psychological, health, physical and daily living, patient care and support and sexuality. The prostate-specific part is composed of eight questions and concern, inter alia, urinary incontinence, urinary symptoms and bowel problems.33 34
The Decision Regret Scale measures distress or remorse after a healthcare decision.35 Respondents will be asked to reflect on their treatment decision, and then asked to indicate the extent to which they agree or disagree with the statements in the regret scale by indicating a number from 1=strongly agree to 5=strongly disagree that best indicates their level of agreement. Regret is measured at 3 months, 6 months and 12 months after the decision. A higher number indicates more regret. A score of 0 means no regret; a score of 100 means high regret.35
Quality of life
The 30-item European Organisation for Research and Treatment of Cancer Quality of life questionnaire- Core questionnaire (EORTC QLQ-C30) includes a global HRQOL scale (two items) and comprises five functional scales: physical functioning (five items), role functioning (two items), emotional functioning (four items), cognitive functioning (two items) and social functioning (two items). There are three symptom scales: nausea and vomiting (two items), fatigue (three items) and pain (two items) and six single items relating to dyspnoea, insomnia, loss of appetite, constipation, diarrhoea and financial difficulties.36
The 25 items prostate-specific module of the European Organisation for Research and Treatment of Cancer Quality of life questionnaire- Prostate cancer questionnaire (EORTC QLQ-PR25) is a self-administered questionnaire that includes four subscales for assessment of urinary symptoms (nine items), bowel symptoms (four items), hormonal treatment-related symptoms (six items) and sexual activity and function (six items). Each of the items can be scored from 1 to 4 (1=not at all, 2=a little, 3=quite a bit and 4=very much). All items and scale scores of the EORTC QLQ-PR25 are linearly transformed to a 0–100 scale based on its scoring manual. Higher scores reflect either more symptoms (urinary, bowel and hormonal treatment-related symptoms) or higher levels of functioning (sexual activity and function).37
Satisfaction with the intervention
With a study-specific questionnaire, information on the experience of the use of the PDA is obtained, and the degree of appreciation for the PDA is asked.
Using the Satisfaction with Cancer Information Profile (SCIP-B) information regarding satisfaction is evaluated. The SCIP-B has previously been shown to be a valid and reliable measure responsive to changes in patient satisfaction over time. It can be used to guide the tailored provision of treatment information to patients. The SCIP-B is a 7-item Likert-type scale (very dissatisfied to very satisfied). A higher score means a higher satisfaction.38
The Preparation for Decision Making Scale (Prep-DM) assesses a patient’s perception of how useful a PDA is in preparing the respondent to communicate with their HCP at a consultation visit and making a health decision. Items can be summed and scored (sum the 10 items and divide by 10). Scores can be converted to a 0–100 scale by: subtracting 1 from the summed score mentioned before and multiplying by 25. Higher scores indicate higher perceived level of preparation for decision making.39
Through a study-specific questionnaire based on the study of Légaré, we examined the reasons for using or not using the PDA.40
Direct medical and direct non-medical cost data are collected with the Trimbos and iMTA Questionnaire on Costs Associated with Psychiatric Illness (TiC-P) using the quality of life assessed with the EuroQol-5 domains (EQ-5D) for the benefit of cost analysis.41 Indirect non-medical cost data related to production losses through work loss days and work cutback days will be sampled with the appropriate PROductivity and DISease Questionnaire (PRODISQ modules).42 Indicators of return to work are: time to partial and to full return to work, meaning number of calendar days between end of treatment and first day at work and time to full return to work corrected for partial return to work. The costs leading up to treatment are measured with the baseline questionnaire (the previous 3 months).41–45
Primary outcome measures partners
With a study-specific questionnaire, information regarding the preferred (treatment) option is obtained retrospectively. The four-item questionnaire contains questions about which of the four treatment options are open for the patient, which preference the partner of the patient had directly after diagnosis (retrospectively) and which preference the partner of the patient has today. In addition, the degree of preference is asked.
Experienced participation and approach to decision making
For the degree of different roles in decision-making involvement, a study-specific questionnaire based on the Deber-Kraetschmer Problem-Solving Decision-Making Scale (four items) supplemented with study specific questions (two items) will beused to examine the role partners play in treatment deision making and the relation with the information received. In addition, the influence of the HCP and their partner on the choice is added to this questionnaire (three items).31
Secondary outcome measures partners
Quality of life of partners
The SF-12 (Short Form Health Survey) contains 12 questions and consists of eight dimensions: physical functioning, role limitations due to physical problems, bodily pain, general health, vitality, social functioning, role limitations by emotional problems and mental health. This instrument measures the quality of life, as it is experienced by the partners.
The SF-12 is a shortened version of the SF-36. Both positive and negative aspects of health are included. For each dimension, the scores are summed at the items and transformed to a scale from 0 to 100. A higher score means better health status.46
Effect of prostate cancer in the relationship
Using a study-specific questionnaire based on the study of Zeliadt, partners and patients will be asked what the impact of the diagnosis of prostate cancer in their relationship has been.21
Communication between patient and partner and interaction with HCPs
Using a study-specific questionnaire based on the study of Zeliadt, patients and their partners will be asked about their communication with each other about prostate cancer. Additionally, partners will be asked about their interaction with HCPs.21
Social contacts and support
For the degree of support provided for and dealing with the patient, we made use of the Active Engagement Scale (AES). The AES measures different styles of behaviour support. Five items form the active involvement scale, eight items measure protective buffering and six items measure protection. The questionnaire contains 16 items with a 5-point scale ranging from 1=never to 5=very often. The last three items are scored on a 5-point scale ranging from 1=no to 5=very strong.47
Role as caregiver
Using the Caregiver Strain Index (CSI) the role of the partner as caregiver is examined. The CSI is a questionnaire containing 13 items, which can be used to measure the degree of care. The following domains are examined: employment, financial, physical, social and time. Positive responses to seven or more points on the index point means a higher level of tension.48
Satisfaction with the intervention
The same items used in the questionnaire for patients as mentioned above, are examined in the questionnaire for partners.42–44
A study-specific questionnaire comprises questions about sociodemographics (age, marital status, family situation, education level). Clinical characteristics (ie, information on date of diagnosis of prostate cancer, treatment, Gleason score and PSA) of patients included in the study will be retrieved from the hospital information system.
The Monitoring and Blunting coping styles survey (The Threatening Medical Situations Inventory (TMSI) questionnaire) examines the information seeking style of people in certain threatening situations. There are two types of information-seeking styles that can occur: information seekers (monitoring strategy) and information avoiders (blunting strategy). In a threatening situation, both strategies can be used interchangeably.49 We hypothesise that information seekers will have less decisional conflict than information avoiders.
The same moderating factors as mentioned above for patients are examined in the questionnaire for partners: sociodemographics (age, gender, marital status, family situation and education level) and monitoring and blunting coping styles.49
For the implementation rate of the PDA we will divide the number of patients who will receive the PDA by the number of eligible patients estimated from the Netherlands Comprehensive Cancer Organization Registry.50 More specifically, the numerator is the number of patients who will receive the PDA. The denominator is the mean number of eligible patients with a localised form of prostate cancer (clinical stage T1c to T3b; T4, N1 and M1 are excluded) per hospital over the preceding 6 years, corrected for the period of inclusion (2 years).
Measurement Instrument for Determinants of Innovation
After using the PDA for 3 months, a questionnaire will be sent out to all participating HCPs. The implementation process and the actual use of the PDA are evaluated with this questionnaire measuring determinants of innovation (MIDI) among HCPs with regard to their experiences and the use of the PDA in the participating centres. This questionnaire is intended to identify the barriers and facilitators at the level of the innovation (use of the PDA), the user (HCP) and the organisation (hospital).51
The primary outcome measure in this study is the patient’s score on the DCS. For the power calculation, we used results from the study of Stacey et al.8 We assume an average score of 29.5 on the DCS in the usual care condition with a SD of 18.25. A decrease to an average DCS to 23.5 when using the PDA is considered clinically relevant, as was the result in the study of Stacey et al.8 The SD is set at 12.5 for the intervention condition.4 To achieve 80% power and using an independent sample t-test and a two-sided significance level of 5%, a standard randomised clinical trial will require 216 patients (108 in each arm). To account for clustering, the sample size was increased. Assuming an average cluster size of 24 patients per hospital and an intraclass correlation of 0.05, a total of 465 patients are needed. As the stepped-wedge design will result in less power than a standard randomised clinical trial but more power when compared with a cluster randomised trial (with number of clusters and cluster size equal to the stepped wedge design), we chose to be conservative and aim for the sample size required for the cluster randomised trial.
The primary analysis (difference in mean DCS between usual care and intervention group) will be done using the mixed-model analysis. Intervention will be included in the model as a fixed factor. A random effect for hospital will be included in the model to account for between-hospital heterogeneity. In addition, time between inclusion of the patient and start of the study and the time between inclusion of the patient and implementation of the PDA in the hospital will be included in the model, if necessary, to correct for fluctuations over time (independent of treatment) and dependency of the intervention effect on time since implementation.
Dichotomous outcomes (such as yes/no questions about the decision) that are measured only one time during follow-up will be analysed using generalised estimating equations. An exchangeable correlation structure will be used (to model within-hospital correlation).
Repeatedly measured continuous outcomes (such as quality of life) will be analysed using mixed models in which in addition to a random effect for hospital also a random effect for patients (nested within hospitals) will be included in the model. The models will include an effect of time since inclusion and the interaction between time and intervention to test whether the course of the outcome over time differs between control and intervention condition.
Although this is a randomised study with measurements under control and intervention conditions in all participating centres, confounding may still occur because of the relatively small number of clusters that is randomised. Confounding will be checked and adjusted for in the analyses by including candidate confounders as fixed main effects in the models. Baseline characteristics of patients in intervention and control condition will be compared using independent t-tests and adjusted for when necessary.
We will record the percentage of drop-out and missing at each follow-up time point. If necessary, we will either use imputation techniques or sensitivity analyses to assess the impact of missing data on our conclusions.
The economic evaluation will be carried out using the applicable guidelines.43 44 The societal perspective will be taken encompassing direct medical costs, direct non-medical costs and indirect costs. Units of resource use (doctor visits, treatment costs, hospital days, hours of work absenteeism and so on) will be multiplied by their appropriate integral cost prices.43 44 Production losses will be economically valued using the friction cost method.44 52 With respect to the PDA, a bottom-up estimation of intervention costs and dissemination will be made. Costs and effects will be analysed simultaneously by calculating the incremental cost–effectiveness ratio (ICER) as the ratio between the difference in total costs and the difference in quality adjusted life years, as assessed with the EuroQol-5 domains (EQ-5D),45 between the two trial arms. The difference in administered treatments between patients in the intervention and control arm is implicitly taken into account through the impact of treatment on health-related quality of life. A 95% CI of the ICER will be calculated using 5000 bootstrap replications. The bootstrap results will be projected on a cost-utility plane, and cost-utility acceptability curves will be plotted against different willingness-to-pay ceilings.53 A sensitivity analysis will be conducted to study the effect of uncertainty in main cost drivers.
Ethics and dissemination
The Medical Ethics Committee of VU University Medical Center (Amsterdam, The Netherlands) has confirmed that the Medical Research Involving Human Subjects Act (WMO) does not apply to this stepped-wedge trial (reference number METC 2013–444). This study will be conducted in accordance with local laws and regulations of the Medical Ethics Committee of VU University Medical Center, Amsterdam, The Netherlands. Eligible patients will fully be informed about the study and asked to participate. The patients will receive a patient information letter and will be informed by telephone about the implications of participation. Patients will have sufficient opportunity to ask questions and to consider the implications of the study before deciding to participate. Before participation, patients will provide written informed consent, compliant with the local and ethical regulations. Patients will be allowed to withdraw from the study without giving a reason, at any time. The results arising from this stepped-wedge trial will be presented at scientific meetings and published in peer-reviewed journals. There is no intention to use professional writers and authorship will be based on the International Committee of Medical Journal Editors guidelines.
We thank all the participating HCPs for the inclusion of patients. This study is part of a larger research project on the implementation of DAs for prostate cancer in three regions in the Netherlands (the JIPPA study), co-initiated and funded by CZ, a not-for-profit Health Insurance Company. We thank dr. Linda van Mierlo from CZ for her efforts in bringing the three research groups together and for the useful input and critical feedback we received during the progress of this project. In addition, we would like to thank Astellas Pharmaceuticals for the co-funding of this project.
Contributors HHMA, CFvU-K, PMvdV, VMHC, ANV, JAN, JAvM and IMV-dL contributed to the design of the study. HHMA is conducting this study in fulfilment of a PhD and will be responsible for data collection, analysis and interpretation. The present manuscript was drafted by HHMA, CFvU-K, PMvdV, VMHC, ANV, JAN, JAvM and IMV-dL. All authors revised this manuscript critically. All authors have read and approved the final manuscript.
Funding This research project is funded by the CZ Innovation Fund (grant 2013–00070) and co-funded by an unrestricted educational grant from Astellas Pharmaceuticals (grant PAS-596). These funding sources had no involvement in data collection, analysis, the preparation of this manuscript or the decision to submit the article for publication.
Competing interests None declared.
Ethics approval The Medical Ethics Committee of VU University MedicalCenter (Amsterdam, The Netherlands) has confirmed that the Medical Research Involving Human Subjects Act (WMO) does not apply to this stepped-wedge trial.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement Data will be available in a machine-readable database, fully anonymised in order to guarantee security and anonymity to the participants. The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request. The (intellectual) property rights with regard to the generated data will rest at the VU University Medical Center, Amsterdam, The Netherlands. Interested parties can request a non-exclusive licence for research and educational purposes. The non-exclusive licence may only be requested after the completion of the thesis to be written reserving the generated data.
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