TY - JOUR T1 - Users’ evaluation of Japan’s cancer information services: process, outcomes, satisfaction and independence JF - BMJ Open Quality JO - BMJ Open Qual DO - 10.1136/bmjoq-2021-001635 VL - 10 IS - 4 SP - e001635 AU - Chikako Yamaki AU - Tomoko Takayama AU - Masayo Hayakawa AU - Fumihiko Wakao Y1 - 2021/12/01 UR - http://bmjopenquality.bmj.com/content/10/4/e001635.abstract N2 - 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.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. ER -