Objectives To investigate women’s understanding and attitudes towards the National Cervical Screening Program (NCSP) and to explore methods to improve screening participation.
Design Semi-structured face-to-face interviews were conducted through convenience and snowball sampling. Thematic analysis occurred using the interpretivist framework.
Setting A private general practice in North Queensland.
Participants Women between the ages of 18 and 74 who attended the general practice were eligible to participate. Fourteen women between 20 and 58 years old were interviewed.
Results Participants were concerned that the new NCSP would miss cancer due to longer screening intervals and reliance on primary human papilloma virus (HPV) testing. They believed that young women are at increased risk of cervical cancer, due to perceived HPV vaccine ineffectiveness and parent objection to vaccination. Most participants were not agreeable to self-sampling and preferred their doctor to perform screening. Personal and practitioner beliefs influenced a woman’s screening participation. Personal factors include being healthy for themselves and their family, previous abnormal smears and family history of cancer. Emphasis was placed on feeling ‘comfortable’ with their practitioner which included patient rapport and gender preference. Proposed methods to improve cervical screening included education programmes, advertising campaigns, general practitioner interventions and improving accessibility.
Conclusions It is apparent that women are hesitant about the new NCSP. However, when provided with additional information they were more amenable to the changes. This highlights the need to improve awareness of cervical screening and the new NCSP.
- community gynaecology
- public health
- gynaecological oncology
- preventive medicine
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Strengths and limitations of this study
Interviews explored participants’ attitudes towards the new National Cervical Screening Program, where there is currently little research.
Individual interviews were conducted until theoretical data saturation and the interview template was piloted.
Convenience and snowball sampling through a private general practice may have led to inaccurate sample representation.
Most participants were well-screened for cervical cancer, which may not be inclusive of high-risk groups.
The study was completed in an outer regional centre and may not apply to the general Australian population.
While the National Cervical Screening Program (NCSP) has more than halved cervical cancer mortality, only 54%–56% of eligible Australian women1 participated in screening between January 2016 and June 2017. This is especially concerning as over 90% of women diagnosed with cervical cancer were under-screened or never-screened.2 Women from lower socioeconomic status, rural areas or those that identify as Aboriginal and Torres Strait Islander have lower screening participation rates and higher cervical cancer mortality.1 Recently, the NCSP has been changed and has moved away from traditional pap smears, towards a 5 yearly cervical screening test (CST) for human papilloma virus (HPV) with reflex cytology.2 Australian women begin cervical screening at 25 years old and have an exit CST from 70 to 74 years old. Women over 30 years who have never been or are currently under-screened are also eligible for self-sampling, consisting of a high vaginal swab for HPV.2 3
As per the WHO guidelines, there has been a global shift to HPV-based cervical screening.4 Worldwide, countries including the UK, Ireland, Netherlands and Turkey have implemented national HPV-based cervical screening, with many more transitioning towards primary HPV testing.5 6 Previous international studies stated most women are unaware of the use of primary HPV testing7 and that some women may experience a negative emotional response towards primary HPV testing as it is a sexually transmitted infection.8 9 Due to the recent nature of changes to cervical screening, there is limited qualitative literature assessing Australian women’s attitudes towards the new NCSP. One Australian study used thematic analysis of an online petition against the new NCSP, revealing that the greatest concerns were missing cancer due to prolonged screening intervals and the delay in screening age.10
The researchers’ primary aim is to explore North Queensland women’s awareness and perceptions of the new NCSP. Knowledge of cervical cancer, factors that affect screening participation and methods to improve screening awareness were also investigated.
Authors followed the Consolidated Criteria for Reporting Qualitative Health Research (COREQ).
Patient selection and setting
Women between 18 and 74 years old who attended a specific North Queensland general practice were eligible for this study with convenience and snowball sampling. This project was conducted with a concurrent quantitative survey. Receptionists provided waiting room surveys and an expression of interest form for a follow-up interview. Quantitative results collected through waiting room surveys will be published separately. The interviews were advertised on the practice’s Facebook page and participants were encouraged to promote the study to their family and friends. Women who expressed interest were contacted by phone or email.
A semi-structured, face-to-face individual interview was conducted at the participant’s convenience at their home or a hospital meeting room between March and April 2019. The average length of the interview was 20 min. All interviews were conducted by the primary author, a female medical student (AN) with training in qualitative research. The interviewer (AN) may have some personal bias as she is eligible for cervical screening. No participants were known to AN and participants were aware that this interview was part of an Honours project.
The piloted interview guide included questions about knowledge of cervical cancer and screening, opinions regarding the NCSP, barriers to screening and thoughts to improve screening participation. During the interview, participants were asked their opinions of the new NCSP, both with their baseline knowledge and after the interviewer provided basic information on the programme. Additionally, the interviewer determined screening status in the interview. Screening status was defined using the previous guidelines due to the current transition to the new NCSP. A ‘well-screened’ participant had undergone cervical screening in the last 2 years while, an ‘under-screened’ participant was overdue for screening.
The interview guide (online supplementary appendix 1) was developed after analysis of the existing literature11 12 and discussion among the investigators, including a general practitioner and a research officer, both experienced in qualitative research. Prior to the interview, participants signed a consent form for the interview to be audio-recorded. The interviews were transcribed verbatim, including notes on non-verbal cues and were uploaded to NVivo. Transcribed interviews were not returned to participants for comments as there was no ambiguity that required clarification. Further, some methodological literature suggests it may provide little benefit to improving data accuracy and it may lead to misrepresentation of the original data.13 No repeat interviews were conducted. Data collection continued until theoretical data saturation was achieved.
Patient and public involvement
No participants were involved with the development of this study protocol or data analysis.
Transcribed interviews were analysed using NVivo V.1214 using thematic analysis and the interpretivist paradigm. Data was analysed under relevant headings, for example ‘Attitudes towards NCSP’ and ‘Factors affecting screening participation’ but no themes were predetermined. AN completed line-by-line coding to identify the preliminary themes and codes in the data, which were validated by another author (JB) with no significant changes to coding required. Data was further analysed to cluster themes under the appropriate research questions to create a thematic schema.
Twenty-eight women expressed interest to be interviewed and were contacted by phone or email. Fourteen women consented to be interviewed, with four participants identified by convenience sampling and ten by snowball recruitment. Table 1 displays individual participant characteristics. The age of participants ranged between 20 and 58 years old. Most women participated in screening and only two were considered under-screened as per the previous NCSP.
Thematic analysis revealed three major themes on participant’s attitudes towards the NCSP: ‘fear of missing cancer’, ‘younger women are at greater risk’, ‘self-sampling’ and ‘change is good’. Screening beliefs were subdivided into personal and practitioner factors. Based on participants’ suggestions, four potential intervention strategies emerged. Table 2 displays illustrative quotes for these themes. A thematic schema depicting conceptual links throughout the themes is displayed in figure 1.
Knowledge of cervical cancer and NCSP
Participants identified genetics and infection as the main causes of cervical cancer. Most participants did not specify HPV as the main cause of cervical cancer but when asked, participants were frequently aware of the link between HPV and cervical cancer. Hormones, contraceptive pill, smoking and toxins were listed by participants as causes of cervical cancer. Women considered family history and sexual activity as the main risk factors for cervical cancer. Other risk factors included not participating in regular screening, previous abnormal smears and being unvaccinated. Participants believed abnormal bleeding and pain were symptoms of cervical cancer though, many women were unsure of the symptoms. Bloating, abnormal discharge and pain during sex (dyspareunia) were also reported by some participants as symptoms of cervical cancer.
Participants understood that cervical screening occurs using pap smears and often could describe that pap smears look for abnormal cells. Some participants were aware of the change to screening and could correctly identify that screening now occurs 5-yearly. Women stated that cervical screening should occur in their early twenties and some said that it began with the onset of sexual activity.
Attitudes towards the new NCSP
Fear of missing cancer
Participants were anxious that 5 years was ‘a long time for cancer to grow’ (P12) and may lead to more women diagnosed with cancer. More regular screening was identified as having ‘a better chance of picking something up’ (P14) as ‘things in our body change very quickly’ (P1). There were fears that increased screening intervals may miss cancer, as clinicians may not always get a ‘clear swab’ (P8) and hence more regular screening was preferable. Additionally, participants were apprehensive that primary HPV testing would miss cancer caused by ‘things other than HPV’ (P9). They were uncomfortable with the CST not testing for abnormal cells as ‘I could be that one percent’ (P12) with cervical cancer not caused by HPV. Subsequently, some participants preferred cotesting for both HPV and abnormal cells to receive the benefits of both screening methods.
Women believed that ‘every 2 years is easy enough to recall but not 5 years’ (P12) and may not remember to participate in screening, due to increased screening intervals. Participants were concerned that increased screening intervals will make women more ‘complacent’ (P12) in their screening behaviour and will delay screening even longer. They proposed that increased intervals required a register to provide appropriate reminders to women. A participant stated that increased intervals may also affect the feasibility of contacting patients, as after 5 years ‘not everyone lives at the same address’ (P7).
Those with a history of previous abnormal smears thought 5 yearly screening was ‘a little bit concerning’ (P8). Participants who had family or friends with cervical cancer were concerned by the increased screening interval as ‘they didn’t pick up hers until it was too late’ (P4). One participant negatively viewed delaying screening until a woman is 25 years, as her friend was diagnosed with cervical cancer earlier than this, and ‘if they didn’t catch it early, she’d be dead’ (P2). These personal experiences with abnormal smears or cervical cancer made women more ‘paranoid’ (P4) about cervical cancer.
Young women are at greater risk
Participants perceived that commencing screening from 25 years old, placed women at increased risk for cancer due to earlier sexual activity of young women. Participants stated that children are ‘having sex a lot younger nowadays’ (P13). They highlighted that as young women are sexually active from their early teens, it may be ‘over 10 years that kids are sexually active before they have screening’ (P3). Participants also believed that delaying cervical screening would prevent opportunistic testing for sexually transmitted infections in young women.
While some women identified that the introduction of the Gardasil vaccination was beneficial in reducing cervical cancer incidence, there was also a perception that ‘a lot of parents won’t let their kids have that’ (P5). This raised concerns as to whether unvaccinated women would be protected under the new NCSP in the future. Additionally, participants feared that ‘even though you are vaccinated you can still get diseases’ (P7) and believed that delaying screening will lead to cervical cancer being missed in women under 25 years. Some participants thought that patients diagnosed with cancer are becoming ‘younger and younger’ (P2). Younger women were described to be at ‘higher risk’ (P2) of cervical cancer and participants felt that earlier detection of cervical cancer in women would improve their survival rates.
Change is good
Several participants expressed their ‘faith in the doctors’ (P11) and believed that screening would not have changed without underlying improvements in science. They perceived that ‘testing is that good’ (P7) if screening intervals have increased from every 2 years to 5 years. Participants highlighted that HPV testing is a positive change as it would ‘catch it (HPV)’ (P11) before abnormal cells became detectable by a traditional pap smear. They accepted that if HPV was ‘linked so strongly’ (P9) with cervical cancer, primary HPV testing was a beneficial change to cervical screening. After participants were provided information on the new NCSP and cervical cancer’s slow progression, they were more receptive towards the new guidelines. An additional benefit of the new NCSP was that reduced screening would ‘make life easier’ (P6) for women, as cervical screening was described as ‘uncomfortable’ (P14) by participants.
Participants were generally hesitant to accept self-sampling as they did not ‘feel confident enough in myself’ (P14) to administer the test. This stemmed from the fear of incorrectly completing the test as they may not ‘swab far enough’ (P5) or that ‘it might be contaminated’ (P4). Doctors were thought to be better equipped to perform cervical screening as they had appropriate training to ensure it was ‘done properly’ (P8). It was perceived that doctors had better visualisation of the cervix as they used a speculum and would take a sample from ‘the right places’ (P3).
Nonetheless, participants acknowledged that self-sampling would provide women ‘more privacy’ (P10) and could improve screening participation. The test was deemed to be ‘less invasive’ (P5) than traditional cervical screening, especially for those who have had previous negative experiences with cervical screening. Participants often had the misconception that self-sampling required a cervical swab. When informed it was in fact, a high-vaginal swab more participants reported they would consider self-sampling. Some participants indicated that they would complete self-sampling if they were provided instructions or shown by a practitioner. Women highlighted that technological improvements allowed for ‘smaller traces’ (P2) of HPV to be detected and this made self-sampling more acceptable.
Factors affecting screening participation
Participants explained that cervical screening was a part of their normal health ‘routine’ (P11). Screening allowed them to have ‘peace of mind’ that they were healthy, and it allowed them to receive ‘further help’ (P1) if required. Many women emphasised that their family was the key reason they had cervical screening. They described their sense of responsibility to their family who required them to ‘make the right choices’ (P3) by undergoing screening. Participants disclosed that cancer could destroy their families and thus they chose to screen. A woman’s personal experiences with cancer shaped her willingness to participate in cervical screening. A history of abnormal smears motivated women to ‘keep on top’ (P13) of their screening to prevent reoccurrence. Women with a family history of cancer had firsthand experience as to how it devastated their families, which motivated them to undergo regular cervical screening.
Several participants described feeling ‘comfortable’ (P10) with their general practitioner as a facilitator to screening participation. This feeling of being ‘comfortable’ was influenced by the doctor’s bedside manner, professional behaviour and hygienic technique throughout the procedure. Some women expressed that they trusted their regular doctor due to their pre-existing relationship, as they have known them for a ‘long time’ (P4). Participants frequently mentioned their practitioner’s gender when discussing screening participation. Most participants indicated that they are more ‘comfortable’ with a female doctor as she ‘has the same bits’ (P2). However, some women had no gender preference as cervical screening is ‘just something that happens’ (P7) and one participant thought that ‘once you have a few kids, you’re over it’ (P4).
Improving CST awareness and participation
Cost and accessibility
A lack of bulk-billed services in regional areas was identified by women as a key barrier to cervical screening participation. The cost of cervical screening was a ‘deterrent’ (P5) for attending the general practitioner for screening, especially in low socioeconomic women as ‘their priority is probably not money for them, it’s going to be feeding their children’ (P5). Participants also emphasised that cervical screening is not bulk-billed, unlike breast and bowel cancer. Women expressed the need for increased accessibility of cervical screening, especially in regional communities. It was suggested that cervical screening should have ‘pop-up’ (P9) clinics, as seen with blood donation and breast screening.
The role of a media campaign to potentially increase cervical screening awareness was discussed by participants. Participants proposed that television advertisements should be aired to encourage discussion about screening. Social media was deemed to be a valuable platform to educate women about cervical screening due to its ‘really big role in young women’s lives’ (P9) and the interaction remained ‘private’ (P2). Women also suggested that an ambassador should lead the discussion on cervical cancer, such as in England when a celebrity ‘found out on Big Brother that she had cervical cancer’ (P3). Participants expressed that it is important to hear personal stories from survivors as it provides a ‘scare factor’ (P8) and would encourage screening.
Participants explained the importance of education to improve screening participation, especially though sex education in schools to ensure young women have the ‘right information’ (P5) about HPV and cervical cancer. Education programmes should inform women about the purpose of the Gardasil vaccine, the NCSP and symptoms of cervical cancer. Participants believed that education will reduce any fears related to screening and solidify ‘how important it is’ (P12). It was also suggested that education sessions should also occur at universities, playgroups and the workplace.
Participants emphasised the importance of their general practitioner as a trusted source of information about cervical screening as ‘you listen to them’ (P6). It was indicated that general practitioners should facilitate opportunistic discussions about screening, especially when a woman turned 25 years old. Practices should display information in the waiting rooms and provide written information such as pamphlets or fact sheets, with this information being ‘very direct, black and white’ (P1) to increase the likelihood that a woman will read it. It was also proposed that general practices should provide information by phone or email.
It became apparent that women were hesitant about the new NCSP, as they were apprehensive that screening will miss cancers due to primary HPV testing and increased screening intervals. A Canadian study by Ogilvie et al stated that primary HPV testing was acceptable, though acceptability decreased when combined with increased screening intervals.15 Participants’ objections towards the change in screening may be due to the general public’s fatalistic view of cancer and belief that frequent testing leads to earlier diagnosis.16 A qualitative Irish study highlighted that even when women understood HPV causes cancer, they were anxious about screening changes due to their attachment to traditional pap smears.17 Participants were afraid that the new programme would endanger young women as they were perceived to be at increased risk of cervical cancer. This was due to participant concerns that young women are becoming sexually active earlier and queries over the effectiveness of the Gardasil vaccine. In reality however, women over 50 years are at higher risk for cervical cancer and this misconception of age-related risk may indicate the need for more patient education.18 Moreover, the new screening programme is predicted to have a greater impact in cervical cancer mortality in unvaccinated cohorts (36%) over vaccinated cohorts (29%).19
It is noteworthy that participants became more accepting of primary HPV screening after they were provided additional information explaining the new NCSP. This is congruent with Waller et al20 who described that women’s anxieties surrounding HPV reduced as health literacy increased. Participants suggested a variety of methods to improve screening including education programmes concentrating on young women. Minimal education occurs about cervical cancer and HPV in schools. Parents may pereceive it is not their responsibility to educate their children on this topic, though a school-based education programme was an acceptable solution to this.21 Media and social media campaigns were proposed to increase awareness. Participants suggested the use of cancer survivors as ambassadors, though past research has suggested an emphasis on information from organisations over personal anecdotes.22 The general practitioner is a trusted and valued source of information and should provide interventional health education with eligible women.23 24 A systematic literature review explains that patient’s likelihood to participate in preventive screening is linked directly to the quality of discussion between clinician and patient, with an emphasis on shared decision making rather than a simple recommendation.25 More research should occur in general practice to develop and evaluate interventions in an Australian context in order to improve cervical screening.
Finally, logistical concerns prevented women from participating in screening. Previous literature demonstrates that reducing economic and geographic barriers improve disadvantaged women’s likelihood to participate in cervical screening.26 Unlike other government mandated screening programmes, such as bowel and breast screening, women bear the burden of cost for cervical screening when attending their appointment with their general practitioner. Government policymakers should reassess the costs involved in cervical screening and consider expanding the availability of bulk-billed services.
Screening participation is influenced by personal and practitioner factors. A woman’s personal factors include: to be healthy, to be there for family, history of abnormal smears or cancer. A woman’s comfort in her relationship with her practitioner influenced her screening behaviour. This was determined by trust in her regular doctor, gender preference and a general feeling of comfort. A previous qualitative literature review similarly discussed that screening provides reassurance of health. Though unlike this study, it also iterated that the emotional response elicited by the test and previous negative experiences hindered participation.27 This may be as the literature review encompassed studies that included under-screened populations, while this study only included two under-screened women.
This study provides timely qualitative research on participant’s perceptions of the new NCSP and will provide valuable data on these changes. Researchers conducted interviews using a piloted interview template until theoretical data saturation. It was also conducted in parallel to a quantitative study as an explanatory component and allowed for data triangulation. However, sampling at one private regional general practice may have led to a skewed representation of the population and may not include high-risk groups for cervical cancer. In addition, snowball sampling may have led to women with more positive health-seeking behaviours to participate in this project. The use of the interpretivist paradigm may allow for the impact of the primary researcher bias (AN) though, this was minimised by a second author (JB) validating thematic analysis.
Women are apprehensive about the new changes to the NCSP, as they believe that increased screening intervals and primary HPV testing may lead to missed cervical cancers. Personal and practitioner factors affect screening participation, with emphasis on maintaining good health and feeling ‘comfortable’ with their doctor. Cervical cancer participation could be improved by increasing education about cervical cancer and the new NCSP through schools, advertising campaigns and the general practitioner. It was also emphasised that the cost and accessibility of screening should be revised.
The authors would like to thank the staff of the general practice where this study was conducted for their assistance with participant recruitment. We also would like to acknowledge the women who participated in interviews for their time and opinions. Thank you to all those who collaborated on this paper and for those who have taken the time to read it.
Contributors AN designed the study, conducted interviews, transcribed interviews, coded data, conducted thematic analysis and was primary author of the manuscript. RB assisted with logistical considerations for data collection at the general practice. JB assisted with study design, designing the interview template, reviewed thematic analysis and provided intellectual input into the manuscripts. CH assisted with study design, creating the interview template and provided intellectual input into the manuscripts.
Funding This work was supported by the College of Medicine and Dentistry, James Cook University (grant number JCU-QLD-792241).
Competing interests None declared.
Patient consent for publication Not required.
Ethics approval Ethical approval was provided by the James Cook University Human Research Ethics Committee (H7465). Participants completed a consent form that stated that they agreed to a recorded interview.
Provenance and peer review Not commissioned; externally peer reviewed.
Data availability statement Data are available upon reasonable request.
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