Article Text

Download PDFPDF

Users’ evaluation of Japan’s cancer information services: process, outcomes, satisfaction and independence
  1. Chikako Yamaki,
  2. Tomoko Takayama,
  3. Masayo Hayakawa,
  4. Fumihiko Wakao
  1. Institute for Cancer Control, National Cancer Center Japan, Chuo-ku, Tokyo, Japan
  1. Correspondence to Dr Chikako Yamaki; cyamaki{at}ncc.go.jp

Abstract

Background Cancer information service (CIS) programmes are becoming increasingly important because patients need to obtain appropriate information and take an active role in their treatment decisions. Programme evaluation is required to determine the level of satisfaction and quality of experiences of users. The purpose of this study is (1) to identify users’ evaluation of CIS programmes by both satisfaction and outcomes that reflect the quality of experience and impact of using the CIS, (2) to examine the related factors of these evaluation outcomes and (3) to analyse the differences of those relations between patients and families.

Method The self-reported questionnaire was answered by 447 patients and 216 families of patients who used Cancer Information Support Centres (CISCs) at 16 designated cancer hospitals from January 2016 to April 2016. We developed 12 evaluation items, including satisfaction, experience and the impact of using CISC.

Results Respondents evaluated the CISC highly, especially in terms of overall satisfaction, followed by the counselling process. Immediate access to CISC was the strongest factor affecting outcomes. Patients who wanted to consult about ‘disease or symptoms’ or ‘had no specific problem’ tended to provide high scores for some outcomes, but those who wanted to consult about a ‘financial problem’ or ‘discharge or care at home’ provided negative scores. These trends were also observed in families but to a more limited extent.

Conclusion Users’ evaluation of CISCs was sufficiently high in terms of overall satisfaction, showing reasonable scores in outcome levels. Immediate access was the strongest factor affecting outcomes and topics of consultation more directly affected evaluation by patients than by families. The distribution of the scores of the measures and related factors was reasonable. The 12-item measurement tool employed in this study seems to be useful for quality monitoring of the CIS.

  • access to information
  • health literacy
  • quality measurement
  • shared decision making

Data availability statement

No data are available. The datasets analyzed during the current study are not publicly available as they are currently being used in the preparation of manuscript but are available from the corresponding author on reasonable request.

http://creativecommons.org/licenses/by-nc/4.0/

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

Statistics from Altmetric.com

Introduction

Needs for cancer information services

People diagnosed with cancer need a wide range of cancer information at different points, even after their treatment,1 and they also need psychological care.2 3 The growing interest in people taking more responsibility for and being more involved in their health accelerates the need for cancer information, which is the basis of communication with their physicians.4 Advances in cancer care bring wider treatment options, making patients understand more precise and complicated cancer information.5 Cancer information is becoming enriched, but not all information is adequate,6 and the expansion of the internet has caused a ‘flood of information’,5 with many websites of low quality, requiring readers to have high literacy.4 7 8

Not only the patients but also their families are involved in the cancer experiences, and they often act as carers and experience the burden of care.9 10 Families also deal with patients’ emotions in addition to theirs.11 Care burden and psychological distress of families are often overlooked.12 Psychological distress of cancer patients and that of their carers is positively related; therefore, an early intervention is needed to prevent such psychological distress.13 Reducing families’ care burden is also important because it affects both patients’ and cares’ quality of life.9

Cancer information service (CIS) programmes are becoming increasingly essential in most countries14 and multidisciplinary counselling interventions are effective,15 affording a place to talk about cancer issues with anonymity and empathy.3 Perocchia et al16 reported that ‘patient-centred communication has been the key NCI research priority’ (p. 36) and described six core functions (fostering healing relationships, exchanging information, responding to emotions, managing uncertainty, making decisions and enabling self-management) embodied in the role of CIS.

The forms of CIS programmes differ slightly by the health policy and other conditions of a country. The National Cancer Institute (NCI) in the USA has run nationwide CIS programmes since 1975, and provides phone, email and live chats in English and Spanish.16 17 The American Cancer Society also provides a nationwide cancer information helpline in the USA. The CIS in Australia is managed by state and territory cancer organisations and provides a cancer helpline.18 19 A survey in Italy showed that 7 out of 11 designated cancer hospitals provided CIS in 2015.20 Although there are some differences in national operations, the core of the CIS mission is shared internationally. Leading institutions constituted the Union for International Cancer Control in 1996 and established the International Cancer Information Service Group (ICISG),14 and they expressed the core values and shared the key procedures for ensuring high-quality service. ICISG has initiated activities to improve the quality of CIS.

About 30 years later, the Japanese government started to appoint designated cancer care hospitals with the enactment of the Cancer Control Act in 2006 and the Basic Plan to Promote Cancer Control Programs in 2007, and 451 hospitals had been appointed by 2021. To provide CIS programmes, these designated hospitals must station Cancer Information Support Centres (CISCs), with at least two trained cancer information specialists. These information specialists undergo a training programme as cancer information specialists in addition to their original backgrounds as nurses, social workers or psychologists. CISCs are open to any patient with or without patient ID, and people without cancer can also access the CISCs for free.21

Service evaluation and quality control of CIS programmes

Quality control is essential for CIS programmes. Previous studies have attempted to determine the quality of these programmes. Satisfaction surveys are the most common method of evaluation, and the results show that users of CISCs are satisfied with the services and the obtained information.19 22–24 However, there is evidence that the efficacy of the service for patients25 and caregivers is limited.22

Boltong et al23 pointed out that the difficulty of CIS evaluation derives from the lack of outcome measures and barriers to using these measures. They insisted that an appropriate measure is critical for a more consistent evaluation of CIS; based on their qualitative research, they identified four themes: drivers for access, experience of using CIS, impact and an adjunct to cancer treatment.

To understand the CISC function achievement, we develop an original questionnaire of the CISC quality performance checklist according to the verbalised CISC role.21 The purpose of this study is to (1) identify users’ evaluation of CIS programmes through satisfaction and outcomes that reflect the quality of experience and impact of using the CIS, (2) examine the related factors of these evaluation outcomes and (3) analyse the differences of those relations between ‘patients’ and ‘families’.

Methods

Setting and participants

The survey included participants from 16 designated cancer hospitals and was conducted from January 2016 to April 2016. CISCs provide both face-to-face and phone counselling, but we chose participants who just used face-to-face counselling. The consultation records of the 16 CISCs showed that 50.7% of the consultations were conducted face to face, with the ratio of the consultations varying greatly from 16% to 94% across the CISCs.26

The questionnaire was distributed to the participants after obtaining ethical approval from each hospital. All CISC users who were provided face-to-face consultations participated in the survey except for those who met the following exclusion criteria: (1) cannot answer the questionnaire, (2) cannot communicate in Japanese or (3) cannot understand the survey procedure. The cancer information specialists explained the study to CISC users. Those who agreed to participate were asked to complete the questionnaire. Participants consented by posting their completed questionnaires. Among 1090 participants, 685 (62.8%) completed the questionnaires after the consultation and posted them. Among these 685 respondents, 447 were patients and 216 were families. The remaining 22 participants did not have any relationship with patients or did not specify their identities and were, therefore, excluded from the analysis.

Variables

Japanese cancer-designated hospitals constitute a council to strengthen their cooperation. Under this council, the Information and Support Service Panel is formed to improve CISC’s service level and encourage collaboration between each CISC. Information and Support Service Panel approved the tool for social recognition of CISC activities under the National Cancer Control Policy in 2015. This tool consists of measures, including outcome, process, structure and countable activities, and survey outcomes in light of the ‘Prerequisite Condition of CISCs’.21

While developing this tool, ‘CISC missions’ were verbalised in reference to the ICISG’s core values27 and patient-centred communication concepts, as follows:

  1. CISCs can be used by everyone, including patients, families and supporters not registered at that hospital.

  2. CISCs gather and provide information about all phases of cancer trajectory and play roles in ensuring that patients have the right to know about, choose and live their own lives and to empower them to do so.

  3. The role of cancer information specialists is to always support clients, consider the root of their difficulties, inform and help them. CISC information specialists are independent of doctors and nurses who are in charge of patients’ treatment.

  4. CISCs and information specialists contribute to the realisation of a society in which cancer patients can comfortably afford relief. The evaluation of CISCs, including e-missions and overall satisfaction, was measured using 12 items.

As Perocchia et al16 described, CIS has six key functions. It seems that the time span of each function varies because some functions are the process of the counselling itself, while others are the outcome of the counselling. ‘Fostering healing relationships’ and ‘responding to emotions’ are provided through the conversation between information specialists and helpline callers. ‘Exchanging information’ and ‘making decisions’ would be accomplished when the users are well informed and consider their situations throughout the counselling. ‘Managing uncertainty’ may take some time, and ‘enabling patient self-management’ may need practice and more time to be accomplished. CISC has a unique position in the hospital because it is independent of each ward and medical office, and can be used by everyone for free.

The 12 items were grouped under the dimensions: overall satisfaction; process of counselling; short-term, medium-term and long-term outcomes of CIS; and the independent position of the CISC in each hospital.

‘Overall satisfaction’ consisted of two items: ‘do you want to use the CISC again?’ and ‘would you recommend using the CISC to your family or friends?’

‘Process of counselling’ comprised the following three items: ‘did CISC provide a comfortable situation for counselling?’, ‘did the cancer information specialist work sincerely with your problem?’ and ‘did the information specialist provide an atmosphere in which it was easy to speak about everything, even that which is difficult to talk about with doctors or nurses?’.

Outcomes of the counselling were measured as short-term, medium-term and long-term outcomes. Short-term outcomes comprised three items: ‘did you feel you were understood by the information specialist?’, ‘did you receive enough cancer information that you needed?’ and ‘do you feel your problem is being resolved because of this counselling?’. Medium-term outcomes comprised the following two items: ‘did you feel you can receive your medical treatment or home treatment support without anxiety because of this counselling?’ and ‘did your relationship with doctors, nurses and other medical staff get better because of this counselling?’. The long-term outcome comprised a single question: ‘do you feel you will be able to handle yourself when other problems arise in the future?’.

The independent position of the CISC focused on the CISC being an adjunct to cancer treatment: ‘did the cancer information specialist help you independently of and better than the hospital?’.

Response to each item ranked on a 5-point scale: 1—strongly agree, 2—somewhat agree, 3—neither agree nor disagree, 4—somewhat disagree and 5—strongly disagree.

To ensure content validity, during the process of generating these variables, information specialists in the CISCs were appointed to check that the items adequately reflected the ‘CISC missions’ described above.

To consider the criterion validity, correlation of the sum of each outcome was calculated. Scores of correlation between ‘overall satisfaction’ and all other outcomes such as process of counselling, short-term, medium-term and long-term outcomes of CIS and the independent position of the CISC were 0.667, 0.611, 0.578, 0.381 and 0.490, respectively. These scores showed that the outcomes were sufficiently correlated but reflected different aspects of CISCs’ services, and that the correlations were reasonable.

Analysis

Among Boltong et al’s23 four CIS themes, we treated three themes (experience of using CIS, impact and an adjunct to cancer treatment) as outcome-focused elements. In addition, we employed overall satisfaction for comparison with the distribution of previous studies. Boltong et al’s23 drivers for access were treated as independent variables. These variables included experience of using CIS, immediate access and topics to talk about at the CISC.

The relationships among demographic characteristics (age and sex), previous experience of using CISC, immediate access, topics to discuss in the consultation and evaluation of the CISC were examined by logistic analysis. Since the distribution of the evaluation items tended toward ‘strongly agree’, to avoid the ceiling effect, binary variables were defined as ‘people who answered ‘strongly agree’ to all the items of a dimension’ and ‘others’.

Logistic regression was used to examine the relationship between previous experience using CISC and immediate access after controlling for demographic characteristics, such as sex and age. Further analysis was conducted for each topic discussed with cancer information specialists independently after controlling for demographic variables and previous experience using CIS and immediate access. Cases with missing variables were excluded from each analysis.

Results

The demographic data of the study participants are presented in table 1. Families tended to have a higher ratio of female members, are younger, and have a higher ratio of first visits to a CISC. The most frequent topic discussed with CISC cancer information specialists was disease or symptoms, followed by financial problems, but the ratio of discussing discharge or care at home was significantly higher for families than for patients.

Table 1

Background of the study respondents

The distribution of each item is presented in table 2 (patients) and table 3 (families), revealing the same trends: more than 80% of the respondents answered ‘strongly agree’ or ‘somewhat agree’ for 10 out of 12 items.

Table 2

12-item evaluation of CISCs (patient)

Table 3

12-item evaluation of CISCs (families)

When we observe the ratio of respondents who answered ‘strongly agree’ to all the items of each outcome, overall satisfaction was the highest for both patients (64.3%) and families (73.5%), followed by experience of using CISC for patients (59.4%) and an adjunct to cancer treatment for families (63.4%). Impact, which is understood as short-term, medium-term and long-term outcomes, ranged from 39.7% to 28.9% for patients and 51.2% to 30.7% for families.

The results of logistic analysis for the relationship between outcomes and demographic characters or the ‘drivers for access’ are shown in table 4 (patients) and table 5 (families). Among these variables, immediate access to CISC showed the strongest relationship with all outcomes (process, short-term outcomes, medium-term outcomes, long-term outcomes, overall satisfaction and independent position of CISC) for both patients and families. When users had visited CISC before, process of counselling, short-term outcomes, medium-term outcomes and overall satisfaction was high in comparison with those who were new to CISCs, but these relationships were seen only in patients who were not family members.

Table 4

Relation between topics discussed with cancer counsellors and each outcome (patient)

Table 5

Relation between topics discussed with cancer counsellors and each outcome (families and others)

Patients who wanted to consult about disease or symptoms rated the process of counselling, overall satisfaction and independent position of CISC positively. Patients who had no specific problem tended to rate the process of counselling highly. In contrast, users who wanted to consult about financial problems rated the process of counselling and overall satisfaction negatively, and the same trend was seen for those who wanted to discuss discharge or care at home. Families who wanted to consult about disease or symptoms positively rated the process of counselling, while those who wanted to discuss financial problems rated the medium-term outcomes of counselling negatively.

Discussion

Quality of CIS evaluated by users’ satisfaction

In this study, 12 items were used to measure the quality of CIS. The ratio of respondents who answered ‘strongly or relatively agree’ was relatively high for all items, ranging from 67% to 97%, and the proportion that gave this rating for 10 items was above 80%.

The scores in this study indicate that the Japanese CISC service provides sufficient satisfaction compared with the global standard, which has been reported to be relatively high.25 Among CIS users of the NCI, 95% have been reported to be strongly or relatively satisfied.28 For the cancer helpline of the Cancer Council Victoria, 93% of the respondents reported feeling that the helpline had assisted them to feel better about their situation.14 Clinton-McHarg et al25 reported that 83%–96% of callers as caregivers were satisfied with the service in western countries. A survey of the Leukemia & Lymphoma Society reported that among users of the Information Resource Center, 86% felt more hopeful and 83% felt more confident in managing care than before the intervention.29

Usefulness of CISC role-specific evaluation measures

In this study, the process of counselling, short-term, medium-term and long-term outcomes of counselling and independent position of CISC was employed as CISC role-specific evaluation measures. Both patients and families rated rather high the process of counselling and independent position of CISC, while medium-term and long-term outcomes of counselling were rated relatively low. These distribution trends are reasonable, because medium-term and long-term outcomes do not always appear directly after counselling.

The relationship between outcomes and variables treated as drivers for access was also reasonable. The respondents who wanted to consult about disease or symptoms gave higher ratings for the process of counselling (both patients and families) and independence of CISC (patients). In contrast, the ratings of those who wanted to talk about financial problems and discharge or care at home tended to be low in the dimension of the process of counselling. CISCs can provide information about disease or symptoms and give direct advice on the use of medical resources; therefore, disease-related or symptom-related matters have a high chance of receiving appropriate support. Japanese CISCs are located in designated cancer hospitals and this study’s participants used the face-to-face service; these characteristics may be reflected in our results.

However, financial problems are sometimes difficult to resolve through counselling. Japan has a universal health insurance system, and patients apply for a pre-fixed ceiling amount.30 Although the ceiling is set according to the patient’s income, insurance is not affordable for everyone. Some patients and their families face a decrease in income or unemployment, and/or indirect costs derived from cancer.31 In Japan, returning to work with/after cancer treatment has been encouraged since 2012. Nonetheless, a significant number of patients quit their jobs immediately after their diagnosis, and it is difficult for them to find re-employment.32 These difficulties may be related to the low evaluation of CISC services because CISCs could not provide a solution to their difficult situation.

Only patients (not families) who wanted to discuss discharge or care at home gave negative ratings for the process of counselling. This may reflect certain aspects of the Japanese medical and social-welfare service system. Recently, cancer care in Japan has shifted from inpatient to outpatient care, similar to other countries, and patients tend to be discharged before they can get accustomed to their condition, which may result in anxiety. Patients being discharged before they are sufficiently recovered often results in burdening the family caregivers.31 The need for informal caregivers is often ignored and excluded from healthcare planning.33 Patients may feel concern regarding burdening their family caregivers; however, it is difficult for information specialists to provide direct solutions. These circumstances can be attributed to patients’ anxiety after their discharge. Therefore, those who wanted to prepare for their discharge rated the process of counselling negatively because home care burden of their families could not be resolved perfectly in CISC consultations.

The relationship between financial problem and discharge may reflect the evaluation of the Japanese healthcare system rather than the services provided by the CISC. In other words, the responses we received as an ‘evaluation of CISCs’ activities’ may be an overall evaluation of the medical service. We need further research to distinguish the direct effect of CISCs from the medical service as a whole.

As shown in table 5, immediate access to the CISC was the strongest factor for all evaluation dimensions. The findings are consistent with the results of previous studies. It has been reported that accurate and timely information decreases anxiety and fear about cancer,34–36 and immediate access to a self-help support programme indicated a better outcome.37 Treiman et al29 found that telephone helplines could provide ‘timely and accurate information and support’, and our research confirms that ‘timeliness’ is very important for CISC users. This means smooth access to CISCs brings the users benefit as well as results in high evaluation. In other words, it is suggested that systematic procedures are employed to help patients and families with needs visiting the CISCs.

Limitations and implications

Some review articles have discussed the lack of evidence on whether CIS or information provision contributes to users’ health.25 38 This study is based on a self-reported evaluation of CIS and does not employ objective symptoms or established psychological status of CISC users. This means that this study is also limited in the subjective evaluation and cannot provide objective evidence of the usefulness of CIS. Future research on objective variables should examine the evidence of the usefulness of CISCs. However, the purpose of this study was to develop the service quality of CIS, and the scores of the measures and related factors are reasonable. This shows that the measures employed in this study can be used for quality control of CISCs.

Tsianakas et al39 reported that a local survey is useful as a screening tool to identify the problem, but it does not always provide sufficient detail of what to do to improve the service; the authors advised combining open comments and in-depth interviews, which can elicit patients’ whole experiences. Our 12-item survey tool can be employed for screening use, scores of study results can be a benchmark of CISC service quality and each CISC can use this tool in combination with the original feedback systems. Trends of the gradual manner of short-term, medium-term and long-term outcomes, and the distribution of the topics that users want to discuss may reflect the feature of each CISC. For example, CISCs with high proportion of users seeking counsel for physical symptoms and negatively evaluating the CISC experience should reconsider the information specialists’ training, which may bridge the gaps in their medical knowledge. Each CISC score indicates its features, strengths, as well as weaknesses.

Although CISCs in Japan provide counselling not only on site but also by phone, email and fax, this study included only onsite counselling. As mentioned above, half of the consultations were conducted face to face and the ratio of such consultations varied across CISCs. This implies that half of the consultations provided by CISCs were not included in this study. In NCI’s study, the satisfaction level of email and chat users was the same as that of telephone users, but the knowledge improvement level was higher among email and online chat users.17 Further research should be conducted on other types of CISC users in Japan.

Lastly, this survey was conducted in 2016 and since then 5 years have passed. CISCs in Japan started operations in 2006 and the survey reports data from the first 10 years. It can be assumed that the evaluation of CISCs has not differed much in these 5 years. However, the current guidelines for designated cancer hospitals were implemented in 2018, which expanded the role of CISCs to include information prescription about cancer genomic medicine and treatment of rare cancer. We should continuously monitor CISCs’ evaluation by patients and families under their expanded roles.

Conclusion

A 12-item evaluation tool generated based on CISC’s roles and missions was employed for the CISC users’ evaluation survey. Six dimensions were identified to reflect the CISC’s functions. Users’ evaluation of CISCs was sufficiently high in terms of overall satisfaction compared with the global standard. As for the outcome of CISC counselling, short-term outcome was rated the highest, followed by medium-term and long-term outcomes.

Regarding other related factors, timely access is the most important factor affecting all the dimensions of the evaluation. Financial and homecare problems negatively affect the evaluation, and may reflect the difficulty of providing effective resolution by CISCs. Although the related factors reported were similar in patients and families, evaluation by patients was more directly affected by their chosen topics of discussion.

The distribution of the scores of the measures and related factors was reasonable. Thus, the 12-item measurement tool employed in this study seems to be useful for quality monitoring of the CIS.

Data availability statement

No data are available. The datasets analyzed during the current study are not publicly available as they are currently being used in the preparation of manuscript but are available from the corresponding author on reasonable request.

Ethics statements

Patient consent for publication

Ethics approval

This study involves human participants and was approved by Medical Ethical Committee of the National Cancer Center (2015-138). Participants gave informed consent to participate in the study before taking part.

Acknowledgments

The authors thank all the respondents of this survey. They are also grateful to the research coordinators of the National Hospital Organization Hokkaido Cancer Center, Asahikawa Medical University Hospital, Tokyo Metropolitan Cancer and Infectious Disease Center Komagome Hospital, Cancer Institute Hospital of JFCR, Kanagawa Cancer Center, Fujisawa City Hospital, Shinshu University Hospital, Nagano Municipal Hospital, Okayama University Hospital, Japanese Red Cross Okayama Hospital, Kagawa University Hospital, Takamatsu Red Cross Hospital, National Hospital Organization Kyushu Cancer Center, Kyushu University Hospital, Nagasaki University Hospital, and National Hospital Organization Nagasaki Medical Center.

References

Footnotes

  • Contributors CY was involved in the entire process of conducting this research, including designing, data collection, analysis of data and preparation of the manuscript. TT was the co-designer of this study, chief secretariat of data collection admission office and adviser for the analysis and writing processes. MH was the co-secretariat of data collection admission office and adviser for the analysis and writing processes. FW organised the research team and checked and provided advice for each step of the study. Each author contributed sufficiently toward the study’s intellectual content, analysis of data and preparation of the manuscript, and takes public responsibility for it. The authors have also reviewed the final version of the manuscript, believe that it represents valid work and approve it for publication.CY is the corresponding author and guarantor.

  • Funding This study was partly funded by two research grants. One is a Health and Labor Sciences Research Grant to FW (201411024) for conducting the surveys. The other is a Health and Labor Sciences Research Grant (R2-Cancer Control20EA1015) awarded to TT for 'providing individualised high-quality information and support services to cancer patients' for English editing and publishing.

  • Competing interests None declared.

  • Patient and public involvement Patients and/or the public were not involved in the design, or conduct, or reporting, or dissemination plans of this research.

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

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.