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BMJ Open. 2014; 4(5): e004990.
Published online 2014 May 15. doi:  10.1136/bmjopen-2014-004990
PMCID: PMC4025472

The effect of information about overdetection of breast cancer on women's decision-making about mammography screening: study protocol for a randomised controlled trial

Abstract

Introduction

Women are largely unaware that mammography screening can cause overdetection of inconsequential disease, leading to overdiagnosis and overtreatment of breast cancer. Evidence is lacking about how information on overdetection affects women's breast screening decisions and experiences. This study investigates the consequences of providing information about overdetection of breast cancer to women approaching the age of invitation to mammography screening.

Methods and analysis

This is a randomised controlled trial with an embedded longitudinal qualitative substudy. Participants are a community sample of women aged 48–50 in New South Wales, Australia, recruited in 2014. Women are randomly allocated to either quantitative only follow-up (n=904) or additional qualitative follow-up (n=66). Women in each stream are then randomised to receive either the intervention (evidence-based information booklet including overdetection, breast cancer mortality reduction and false positives) or a control information booklet (including mortality reduction and false positives only). The primary outcome is informed choice about breast screening (adequate knowledge, and consistency between attitudes and intentions) assessed via telephone interview at 2 weeks postintervention. Secondary outcomes measured at this time include decision process (decisional conflict and confidence) and psychosocial outcomes (anticipated regret, anxiety, breast cancer worry and perceived risk). Women are further followed up at 6 months, 1 and 2 years to assess self-reported screening behaviour and long-term psychosocial outcomes (decision regret, quality of life). Participants in the qualitative stream undergo additional in-depth interviews at each time point to explore the views and experiences of women who do and do not choose to have screening.

Ethics and dissemination

The study has ethical approval, and results will be published in peer-reviewed journals. This research will help ensure that information about overdetection may be communicated clearly and effectively, using an evidence-based approach, to women considering breast cancer screening.

Trial registration number

Australian New Zealand Clinical Trials Registry ACTRN12613001035718.

Keywords: breast neoplasms ,mammography screening; decision making; informed choice

Strengths and limitations of this study

  • This longitudinal mixed-methods study includes a randomised controlled trial and a qualitative substudy. Participants are sampled randomly and are making real-life decisions. The intervention rests on strong evidence (updated published model of screening outcomes incorporating local data) including extensive qualitative research. The primary outcome is informed choice, and data are collected by an independent non-profit company.
  • Our estimates of the effects of screening are drawn from trials conducted overseas and in the past. The intervention may not address the needs of some population groups such as people with low literacy.

Introduction

While mammography screening can reduce breast cancer mortality, it also carries the risk of overdetection (or overdiagnosis). This occurs when screening detects a cancer that would not have presented clinically during the woman's lifetime, meaning she would never have acquired a diagnosis had she not attended screening. Overdetection and the resulting overtreatment are likely to cause harm in terms of emotional well-being,1 physical health in the short term and long term2 and implications for relatives consequently classified as high risk.3 4

The problems of overdiagnosis and overtreatment in cancer screening5 and the broader health context6 are receiving increasing attention. In the UK, an independent expert panel was commissioned in 2011 to review evidence on important consequences of breast screening, including the challenging task of quantifying the level of overdetection. Wide variations among previous estimates had prompted extensive debate over the appropriateness of different observational methods and their associated biases.7–9 Focusing on randomised trials as the best quality evidence, the panel concluded that invitation to screening leads to overdetection of breast cancer at a rate of 19% during the 20-year screening period.10

Historically, information materials distributed by breast screening programmes worldwide have emphasised benefits and lacked explanation of overdetection.11–14 The appropriateness of explicitly informing people about overdetection has been debated, with reluctance driven by concerns about dissuading women from screening.15 16 However, in the context of a growing international movement towards policies promoting greater involvement of patients and citizens in health decision-making17–20 it has been argued that people offered screening should have the opportunity to make informed decisions about whether to participate.

Making an informed decision about screening requires clear, balanced information on benefits and harms.10 20–23 A new approach to public information was recently adopted in the UK with the aim of better supporting informed choice,24 and the new UK breast screening leaflet released in September 2013 acknowledges overdetection as ‘the main risk of screening’.25 Given the current lack of awareness of overdetection,26–30 such a change to public information is significant and there is a need for high-quality research into its effects. Breast screening is a highly emotive issue, as demonstrated by the public outrage unleashed when the US Preventive Services Task Force changed its recommendations in 2009.31–33 Moves to include overdetection in screening information materials stand to affect large numbers of women around the world. Research is needed to ensure important messages are not misconstrued in ways that adversely affect women's health and well-being.

There is little research on public responses to overdetection. In a focus group study,27 we examined 50 women's understanding of overdiagnosis, screening attitudes and intentions and views on information provision. Participants were previously unaware of overdetection but able to understand it. Although surprised, women valued the information about overdetection. These findings were corroborated by a similar UK study.30 As some women in our study indicated that knowing about overdetection may change their screening or treatment decisions,27 a careful and balanced approach to communication is critical.

The current population-based trial extends our investigation of the impact of overdetection information into a real-life decision-making setting. Using a longitudinal, randomised design incorporating quantitative and qualitative methods, the trial examines the impact of written information about screening outcomes (breast cancer deaths averted and false positives, either including or excluding overdetection) among women close to the target age for entering Australia's screening programme. In addition to examining how the information affects women's decisions, attitudes, psychological responses and well-being in the short term, we will follow participants for 2 years to assess effects on screening participation and to qualitatively investigate the long-term impact of this information in women who do and do not choose to be screened.

Aims

We will examine and evaluate the impact of information about overdetection in breast screening on:

  1. informed choice—measured via knowledge, attitudes and intentions;
  2. decision process (decisional conflict and confidence);
  3. short-term psychosocial outcomes (anxiety, risk perceptions, breast cancer worry, anticipated regret);
  4. screening attendance over 2 years;
  5. experience of screening for those who attend;
  6. long-term psychosocial outcomes (decision regret, quality of life).

Methods and analysis

Study design

The study uses a randomised trial design with conventional quantitative outcomes plus an embedded longitudinal qualitative substudy (streams A (quantitative) and B (qualitative)—see figure 1). This design ensures we can (1) quantify the impact of overdetection information on women's immediate screening decision-making and (2) assess behaviour and psychosocial outcomes throughout the 2-year follow-up period, allowing us to contextualise experiences and capture changes over time among women who ultimately choose to screen or not screen.

Figure 1
Design of randomised controlled trial with longitudinal qualitative substudy.

Since it is plausible that the qualitative interviews could influence responses to the quantitative measures (even by simply reminding women of breast screening), we have separated the cohorts entirely so that our quantitative dataset will not include any women who are part of the qualitative component of the research. Both streams will follow the same procedure including all quantitative measures completed via telephone, but women in the qualitative stream will be invited for additional interviews at the time points specified.

Setting and participants

Study participants will be a community sample of women aged 48–50 years from the Australian state of New South Wales (NSW). The government-funded programme, BreastScreen NSW, offers a free biennial screening service and mails a personal invitation to all women when they turn 50 and enter the target age range. The study will therefore involve women who are approaching or at this decision point. This study focuses on women facing an initial decision about whether to screen, as our qualitative study found that women's perceptions of overdetection were influenced by their previous screening participation.27

Eligibility criteria

Inclusion criteria

Individuals will be eligible if they are women; aged 48–50 years; residing in NSW and sufficiently fluent in English34 to understand study materials and complete telephone interviews.

Exclusion criteria

Individuals will be excluded from the trial if they have a personal history of breast cancer; have had any mammogram within the previous 2 years or are at increased risk of breast cancer compared with the general population, for example due to a strong family history.35 Women at increased risk will be referred to their doctor or the Australian Cancer Council's telephone helpline.

Pilot study

Before the main trial, a pilot study will be carried out with approximately 30 women to test the recruitment and data collection procedures up to the 2-week telephone survey, including checking the suitability of the telephone interview scripts.

Participant recruitment

We will recruit by sampling from a random extract of women in the appropriate age group, drawn from the NSW electoral register. Recruitment will be carried out via telephone by the Hunter Valley Research Foundation (HVRF), an independent non-profit organisation with extensive experience running community surveys and successfully recruiting participants into health research studies.27 36

A database containing names and telephone numbers will be encrypted and sent to HVRF. Trained HVRF interviewers will telephone potential respondents and explain how and why their contact details were obtained. Interviewers will then briefly introduce the study and determine eligibility using a series of simple questions. Eligible women will be informed about what the main study involves and invited to participate. The trial's aims will be described in a general way, as ‘a study to make sure that written information about breast cancer screening is clear and helpful to women’, without specifically referring to overdetection. Consent will be obtained orally and documented by the interviewer.

Preintervention procedure and measures

To achieve a common baseline level of information about screening, immediately after recruitment to the study all women will be sent the BreastScreen NSW programme leaflet, a freely available leaflet that BreastScreen sends to women together with their invitations to attend screening.37 As well as outlining practical aspects of mammography screening, the leaflet describes benefits of early detection while acknowledging the possibility of a false negative (ie, missed cancer) or false positive result (ie, abnormal mammogram when there is no cancer). It does not provide quantitative estimates of the chances of these outcomes, nor does it mention overdetection.

After 1 week HVRF will telephone each participant again, collect demographic information not already recorded, and check that the woman has received the leaflet and had time to read it. If so, the interviewer will collect the following baseline data and then proceed to randomisation:

Stage of decision-making

Women will be asked how far along they are with their decision about screening, using a single item with four response options, as used in previous trials of screening decision aids.38 39

Screening intentions

Women will be asked their intentions about having a screening mammogram within the next 2–3 years, using a single item with five response options (ranging from definitely will not to definitely will).40 41

Screening attitudes

Attitudes towards screening will be measured using a validated, theory-based generic screening attitudes scale comprising six items42 with five response categories ranging from strongly disagree to strongly agree (scored 1–5).36

Screening knowledge (conceptual)

Women's knowledge of the main concepts of screening will be assessed using items adapted from previous decision aid trials.36 38 39

If the woman has not yet read the leaflet, arrangements will be made to call back at an agreed time. If she has still not read the leaflet by the next contact, she will be excluded from the trial (prior to randomisation). The purpose of only including women who have demonstrated a willingness to read study materials is to maximise the likelihood that the individuals randomised will read their allocated intervention and complete the trial, which is designed to detect any intervention effect under ideal circumstances. This is appropriate for the first randomised trial of consumer information about overdetection in breast screening.

Allocation procedures

Randomisation sequences will be generated by a statistician who has no contact with participants, using permuted blocks with sizes of 4 and 8. Interviewers responsible for recruiting participants will not be aware of the randomisation sequence or allocation and therefore will not know which intervention respondents will receive.

Randomisation to stream A versus B

During the second telephone contact, participants will be randomised to either stream A or receive invitation to the qualitative stream B (described by the telephone interviewer as an ‘enhanced version’ of the study) to achieve the desired sample size in each stream (ie, in an allocation ratio of approximately 13:1). Women who accept the invitation to stream B will be sent plain-language written information about the qualitative substudy together with their allocated booklet. Women who decline the invitation to stream B will be included in stream A.

Randomisation to intervention versus control

Participants within each stream will be allocated to either the intervention or control arm using permuted block randomisation with a 1:1 ratio.

Intervention and control arms

The trial will compare two versions of an evidence-based written information booklet explaining the benefit and harms of biennial mammography screening from age 50, cumulated over 20 years:

  1. Intervention: explanatory information and quantitative estimates of breast cancer mortality benefit, false positives (including total number of women with a false positive, and number having a biopsy) and overdetection; versus
  2. Control: the same explanatory and quantitative information about breast cancer mortality benefit and false positives as in the intervention group but with NO overdetection information.

The booklet was developed for the purposes of this study, and is designed to inform but not to influence women either towards or away from screening. The content and presentation were guided by our focus group findings regarding women's understanding of overdiagnosis, areas of concern or confusion, and views on communication (including a preference for the term overdetection rather than overdiagnosis).27 The booklet was developed with input from layperson collaborators, reviewed by independent clinical and communication experts, and thoroughly piloted for acceptability and comprehension (details of piloting will be published separately).

The quantitative evidence presented is based on an updated version of our published model of screening outcomes43 using effect estimates from a meta-analysis of randomised controlled trials,10 adjusted to reflect screening attendance rather than invitation, and applied to current Australian data. The expected frequencies of outcomes are illustrated and contextualised using icon arrays depicting the absolute numbers affected per 1000 women screened over 20 years.44

Table 1 summarises the topics covered in the two versions of the booklet (for additional detail, see online supplementary table). Both are identical in format; the control version was produced directly from the intervention booklet by simply deleting the two pages on overdetection and all other references to it (eg, in Q and A and summary table). The sections on benefit and false positives are identical across versions in terms of content and format.

Table 1
Summary of contents of intervention and control booklets

Stream A: quantitative study

Methods of data collection and blinding

Trained HVRF interviewers will conduct a telephone survey (15–20 min) to collect postintervention outcome data 2 weeks after randomisation, and will carry out further brief telephone surveys for long-term follow-up at 6 months, 1 year and 2 years postintervention. Table 2 lists the study variables and timing for measurement.

Table 2
Summary of study variables and timing for measurement

The HVRF personnel are independent of the research team, and interviews will be conducted within a supervised environment where interviewer performance is regularly monitored to ensure scripts are read as written. All survey questions use standardised wording, and the questions are designed such that the woman's study group allocation is unclear to the interviewer until the final part of the interview.

Outcome measures

Primary outcome

The primary outcome is informed choice—that is, the extent to which women's screening decisions are consistent with their informed values or attitudes.45 46 Informed choice is assessed by combining measures of knowledge, attitudes and actual choice,47 and has been used successfully in previous decision aid studies.36 38 48 Selection of this primary outcome reflects recent international commitments to informed choice as a key marker of quality in screening programmes.

Informed choice will be assessed at 2 weeks postintervention as a dichotomous outcome, and the intervention and control groups will be compared in terms of the proportion of women making an informed choice. To determine whether each woman makes an informed choice we will separately measure, and then combine, three components: knowledge, attitudes and intentions. An informed choice is one in which knowledge is adequate, with attitudes and intentions being consistent (ie, positive attitudes with positive intentions or negative attitudes with negative intentions). For the purposes of assessing informed choice, the knowledge, attitude and intention measures will be dichotomised using an a priori threshold (see below). The three component variables will also be examined and reported separately to enable more fine-grained understanding of the impact of the intervention on decision-making.

Screening knowledge

We will apply a competency-based approach to assess knowledge49 in line with our published knowledge assessment framework.50 Understanding of conceptual and numerical information provided in the study will be measured using items adapted from our previous decision aid trials.36 38 The items are designed to assess understanding of core screening concepts (including mortality benefit, false positives and overdetection) and awareness of the approximate numbers of women affected by particular outcomes. Total knowledge scores will comprise four subscales: conceptual understanding (of general and overdetection-related information) and numerical understanding (general and overdetection related). As in previous decision aid trials,36 38 39 48 knowledge will be scored using a marking scheme developed a priori. The threshold score to be considered adequate for the purposes of determining informed choice will also be set a priori. Women will have to demonstrate a basic conceptual understanding of overdetection, false positives and the mortality benefit from screening to be considered as having adequate knowledge. Sensitivity analyses will examine the impact of using higher and lower thresholds.

Screening attitudes

As at baseline, screening attitudes will be measured using a validated six-item scale.42 Scores on each item range from 1 (strongly negative) to 5 (strongly positive).36 For the informed choice outcome, the threshold for a positive attitude will be a total score of 24 or above (ie, scores of 4 or 5 on the 5-point response scale for each item). As literature shows that screening attitudes are typically very positive,36 38 39 a sensitivity analysis will explore the impact of using a higher threshold.

Screening intentions

Intentions to participate in screening within the next 2–3 years will be measured as described at baseline.40 41 Scores will be dichotomised on the five-point scale as categories 1–3 (responses definitely will not, will not and unsure) indicating ‘not intending’ to screen and categories 4–5 (will and definitely will) as ‘intending’ to screen.

Secondary outcomes

The following outcomes will be measured at 2 weeks postintervention.

Perceived importance of screening benefit/harms

Purpose-developed items will be used to ask women about their personal perceptions of the importance of specific screening outcomes in their decision-making about screening. Women will be asked how important it is for them to consider the chances of (1) avoiding breast cancer death, (2) being diagnosed and treated for a cancer that is not harmful, and (3) having a false positive. The four response options range from very important to not at all important.

Perceived personal chances of screening benefit/harms

Women will be asked about their perceived personal likelihood of experiencing specific outcomes (as above) if they have screening, compared with an average screened woman,51 using five verbal response categories ranging from much lower to much higher.

Decision process

Decisional conflict and confidence will be assessed using the validated and widely used Decisional Conflict Scale (10-item low literacy version)36 52 and Decision Self-Efficacy Scale.36 53

Time perspective

This will be assessed using the four-item short form of the Consideration of Future Consequences Scale,54 55 with five response categories ranging from strongly agree to strongly disagree.

Anticipated regret

Two items from a validated scale will measure anticipated regret about screening (action regret) and about not screening (inaction regret),56 57 with five response categories ranging from strongly agree to strongly disagree.

Perceived personal risk of breast cancer

Women will be asked about their perceptions of personal risk for developing breast cancer in their lifetime, in absolute terms57 (using four verbal response categories ranging from no chance to high chance) and relative to an average woman of the same age58 (using five verbal response categories ranging from much lower to much higher).

Breast cancer worry

A validated single item will measure women's level of worry about developing breast cancer, using four verbal response categories ranging from not worried at all to very worried.36 38 59

Anxiety

This will be measured with the six-item short form of the Spielberger State Trait Anxiety Inventory.36 56 60

Booklet utilisation and acceptability

Acceptability and utilisation of materials will be assessed by items measuring how women used and evaluated the booklets, as used successfully in previous decision aid trials.39 61

The following secondary outcomes will be measured at longer term follow-up.

Screening participation

Self-reported attendance at breast screening will be assessed via telephone survey at 6 months, 1 and 2 years. Previous research has demonstrated that this is a reliable indicator of actual breast screening behaviour in Australia (91% of women reported a mammogram accurately to within a year of the recorded date).62 Attendance at diagnostic mammograms and other breast tests will also be assessed by self-report at these time points, and any relevant diagnoses will be recorded. At the end of the trial we intend to assess participants’ screening attendance from screening records as well.

Decision regret

At 6 months, 1 and 2 years, the Decision Regret Scale63 will measure women's level of regret regarding their initial decision whether to screen or not. The scale has five items and five response categories ranging from strongly agree to strongly disagree.

Quality of life

At each of the long-term follow-up contacts, quality of life will be measured using the Consequences of Screening in Breast Cancer questionnaire, part I.64

Screening knowledge, attitudes, intentions and psychosocial outcomes measured previously

Long-term follow-up contacts will reassess selected outcomes using the same measures as previously (see table 2 for details).

Sample size

The primary analysis will be comparing the two study groups on the proportion of women who make an informed choice, using the χ2 test. We judge an absolute difference of 10–15% to be relevant. Assuming conservatively that one of the group proportions is 50%, in order to achieve 80% power to detect a group difference of 10% with a two-sided significance level of 5%, we require 407 women per arm at the 2-week follow-up. This sample size is sufficient to detect a 10–15% difference in intentions and a mean difference smaller than 0.5 SDs in knowledge, attitudes and psychosocial outcomes (assuming SDs for these scales based on results from our previous trials) which is considered the minimum clinically important difference for psychosocial outcomes.65

On the basis of our previous research using a similar protocol36 and data from HVRF, we anticipate losing 10% of recruited women at the preintervention stage because they do not read initial study materials within the required time frame, and up to a further 10% who cannot be contacted for the 2-week follow-up survey. Therefore to achieve our 2-week follow-up target sample of 814 women in the quantitative stream and 60 in the qualitative stream (see below) we aim to recruit approximately 1078 women into the study.

On the basis of their extensive telephone survey experience, HVRF have estimated a further 20% loss to follow-up at 1 year and an additional 10% at 2 years (total loss to follow-up at 2 years is 30%). The remaining sample should be sufficient to detect a difference of 12% in attendance at 2 years among 285 women per arm (assuming a 30% attrition rate and 47% attendance rate at mammography screening).66

Statistical analysis methods

Analysis will compare the intervention and control groups on an intention to treat basis (ie, all participants, as randomised) and will be carried out blinded to intervention status. We will use the χ2 test to analyse binary outcomes including informed choice, and the two-sample t test for continuous outcomes, with a significance level of 5%. We will use multiple imputation and sensitivity analyses to explore the impact of missing data.

Stream B: qualitative study

We will conduct a longitudinal qualitative evaluation among women randomised to stream B of the trial to explore in depth their responses to information about overdetection—specifically, how they understand the information and integrate it with existing knowledge, and their subsequent intentions and decisions whether to participate in screening. Women will receive an identical protocol to those in the main trial (stream A), including quantitative telephone survey measures. However, we will also carry out face-to-face or telephone interviews among these women over 2 years at time points corresponding with the assessment of self-reported screening behaviour in the main randomised controlled trial (6 months, 1 and 2 years). This will enable us to examine the experience of screening among women who choose to screen with and without exposure to overdetection information (ie, intervention and control groups), to assess whether the information has any positive or negative impact on women's screening experience (eg, the way in which women interpret, cope with and act on their screening results). This will allow a rich and contextualised understanding of women's experiences and decision-making to complement the quantitative data, and will also enable us to examine the experience of women who choose not to screen, including changes in their feelings over time and following the receipt of screening invitations. Based on current participation in BreastScreen we expect between 25% and 50% of the women will choose not to be screened, giving us a meaningful sample of women choosing to screen and not to screen within the qualitative stream.

Methods of data collection

All women will be interviewed either face to face or by telephone, 1–2 months postintervention, by an experienced qualitative interviewer. Subsequent interviews will be conducted by telephone. For participants living outside the greater Sydney area all interviews will be by telephone. Interviews will be audio recorded and transcribed verbatim.

Sample size

The intended sample size in the qualitative stream is 60 participants, of whom approximately 30 will be randomised to each study arm. This is a well-accepted sample size in qualitative studies using in-depth interviews, sufficient to explore variation in experiences among participants.67 68

Qualitative analysis

The study will take a phenomenological perspective and will use framework analysis,69 a widely used matrix-based method of thematic analysis which has been applied successfully in many published qualitative studies.70 71 This method enables qualitative themes to be compared within individuals (eg, a woman's understanding of overdetection and her psychological response to it) and between individuals (eg, comparing women who choose to screen and those who do not). It is particularly useful when working in a large research team to facilitate transparency and rigour in the analytic process, and interpretation of research findings.

Ethics and dissemination

Consent will be provided over the telephone and documented by the HVRF interviewer. Explaining the study and obtaining consent by telephone will facilitate comprehension and reduce the unnecessary burden entailed in a written consent form. All HVRF telephone interviews are administered through a computer-assisted telephone interview (CATI) programme. The CATI and quality control processes used by HVRF ensure that interviewers do not skip any statements while providing information to respondents. Immediately after recruitment, women will be sent plain-language written study information to inform them of their right to refuse participation or withdraw consent at any time, including instructions for how to contact the researchers with questions, withdraw from the study or make a complaint.

The results of the trial will be published in appropriate journals, regardless of the outcomes. The trial will be reported in accordance with the CONSORT Statement.72

Registration details

The trial is registered with the Australian New Zealand Clinical Trials Registry (registration no. ACTRN12613001035718).

Supplementary Material

Author's manuscript:
Reviewer comments:

Acknowledgments

The authors would like to thank Petra Macaskill for her contribution to the study design during the early planning phase, and Jenn Kidd for her contribution to refining the study materials.

Footnotes

Contributors: KMC, JH, LI, AB and JJ developed the original concept of this study. All authors contributed to discussion and revisions to the study design. KMC, AB, JJ, NH, HD and KMG obtained funding. JH drafted the manuscript; all other authors were involved in revision of the manuscript.

Funding: The trial is funded by a project grant from the National Health and Medical Research Council of Australia (no. 1062389).

Competing interests: None.

Ethics approval: The University of Sydney Human Research Ethics Committee has approved the study (project no. 2012/1429).

Provenance and peer review: Not commissioned; externally peer reviewed.

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