Effects of a Provincial-Wide Implementation of Screening for Distress on Healthcare Professionals' Confidence and Understanding of Person-Centered Care in Oncology

Authors:
Rie Tamagawa From CancerControl Alberta, Alberta Health Services, Calgary, Alberta, Canada.

Search for other papers by Rie Tamagawa in
Current site
Google Scholar
PubMed
Close
 PhD
,
Shannon Groff From CancerControl Alberta, Alberta Health Services, Calgary, Alberta, Canada.

Search for other papers by Shannon Groff in
Current site
Google Scholar
PubMed
Close
 MSc
,
Jennifer Anderson From CancerControl Alberta, Alberta Health Services, Calgary, Alberta, Canada.

Search for other papers by Jennifer Anderson in
Current site
Google Scholar
PubMed
Close
 MN, RN
,
Sarah Champ From CancerControl Alberta, Alberta Health Services, Calgary, Alberta, Canada.

Search for other papers by Sarah Champ in
Current site
Google Scholar
PubMed
Close
 RN, BScN, CON(c)
,
Andrea Deiure From CancerControl Alberta, Alberta Health Services, Calgary, Alberta, Canada.

Search for other papers by Andrea Deiure in
Current site
Google Scholar
PubMed
Close
 BA
,
Jennifer Looyis From CancerControl Alberta, Alberta Health Services, Calgary, Alberta, Canada.

Search for other papers by Jennifer Looyis in
Current site
Google Scholar
PubMed
Close
 MPH
,
Peter Faris From CancerControl Alberta, Alberta Health Services, Calgary, Alberta, Canada.

Search for other papers by Peter Faris in
Current site
Google Scholar
PubMed
Close
 PhD
, and
Linda Watson From CancerControl Alberta, Alberta Health Services, Calgary, Alberta, Canada.

Search for other papers by Linda Watson in
Current site
Google Scholar
PubMed
Close
 PhD, RN
Full access

Background: Although published studies report that screening for distress (SFD) improves the quality of care for patients with cancer, little is known about how SFD impacts healthcare professionals (HCPs). Objectives: This quality improvement project examined the impact of implementing the SFD intervention on HCPs' confidence in addressing patient distress and awareness of person-centered care. Patients and Methods: This project involved pre-evaluation and post-evaluation of the impact of implementing SFD. A total of 254 HCPs (cohort 1) were recruited from 17 facilities across the province to complete questionnaires. SFD was then implemented at all cancer care facilities over a 10-month implementation period, after which 157 HCPs (cohort 2) completed post-implementation questionnaires. At regional and community care centers, navigators supported the integration of SFD into routine practice; therefore, the impact of navigators was examined. Results: HCPs in cohort 2 reported significantly greater confidence in managing patients' distress and greater awareness about person-centered care relative to HCPs in cohort 1. HCPs at regional and community sites reported greater awareness in person-centeredness before and after the intervention, and reported fewer negative impacts of SFD relative to HCPs at tertiary sites. Caring for single or multiple tumor types was an effect modifier, with effects observed only in the HCPs treating multiple tumors. Conclusions: Implementation of SFD was beneficial for HCPs' confidence and awareness of person-centeredness. Factors comprising different models of care, such as having site-based navigators and caring for single or multiple tumors, influenced outcomes.

Background

Distress is a significant emotional consequence of the cancer journey,1 with 35% to 60% of patients experiencing distress following their cancer diagnosis.24 Distress is multifactorial,5 and high levels of distress can contribute to more psychosocial problems,6 physical symptoms,7 and poor satisfaction with medical care.8 Furthermore, patient's distress is often unrecognized.9 Research highlights that clinician's accuracy in detecting patients' distress is between 10% to 28%,10,11 with many clinicians reporting that they have received little training in managing psychosocial issues and do not feel confident in dealing with distress.12

Given the negative implications of distress for patients, it has been endorsed as the sixth vital sign.13,14 Many cancer accreditation standards recommend using the approach known as screening for distress (SFD). By identifying, assessing, and acting on patient concerns in the clinical environment, SFD promotes respectful and responsive clinical interactions and shared decision-making, a core component of person-centered care.15 Research indicates that routine SFD improves quality of care, such as patient–provider interactions,16 and symptom management17; however, implementing SFD as a standard of care can be challenging.18

Research has shown the impact of SFD is influenced by program implementation and education about distress management provided.15 Positive effects of SFD were often found when implemented concurrently with other supportive resources.19 Other strategies shown to improve success include staff training and/or using specialized screening staff.1921 Defined leadership among clinicians, project coordination, and strategic quality improvements (QIs) are enablers.22

Previous research also identified barriers to screening. At the provider level, barriers include lack of time, training, confidence,19,23 and a belief that the management of distress is not core to their role.24 Organizational barriers include lack of resources, inconsistent documentation, physician engagement, and the perception that screening may be intrusive in the clinical setting.23,25,26 Nonetheless, clinicians identified that SFD facilitates symptom management, multidisciplinary team communication, and referral practices.16,2729 Moreover, healthcare professionals (HCPs) reported that attending to patients' self-reported concerns enhanced person-centered care delivery.29

This article reports on a provincial QI project designed to establish standardized routine screening and management of distress across all provincial cancer care delivery sites. Rigorous evaluation was conducted to establish the impact on patient-reported outcomes.30 This report focuses on how the implementation influenced HCPs' confidence in identifying and managing distress, and awareness of person-centeredness. Additionally, this project explored the impact that different models of care had on the SFD intervention.

Patients and Methods

Participants

HCPs working in any of the 17 cancer centers across the province were invited to evaluate this provincial QI project.

Procedure

Cohort 1: Cohort 1 was accrued before the implementation of SFD at each respective clinical site between September 2012 and September 2013. Participants were provided a letter of introduction to the project and a provincially standardized questionnaire. All questionnaires were anonymous and returned to program staff once completed.

Implementation of SFD: Following the recruitment of cohort 1, staggered implementation of SFD commenced on November 2012 with a 10-month implementation period at each site. Three project coordinators worked with centers to integrate SFD and to host education sessions. All staff members were included in a 1-hour group education session on person-centered care. Nurses and radiation therapists who would be responsible for the initial review of SFD received a second 1-hour individual or small group education session. This was followed by “just in time” education support in the clinical environment for 2 weeks after implementation. Key elements of education included (1) understanding the standardized SFD tool (Edmonton Symptom Assessment System31 and Canadian Problem Checklist32), (2) facilitating a person-centered conversation,33 (3) assessing the impact of distress and self-management efforts, and (4) engaging in shared decision-making regarding interventions. Education sessions were standardized across the province and developed from the implementation guide for SFD15 and a Web-based education program for SFD.33

Each site integrated the SFD intervention into their routine practice. The clinic receptionist initiated the intervention by asking the patient to complete an SFD form. A trained HCP then reviewed the tool and conducted the SFD intervention. Because different care models exist related to the size and resources available at each site, distress management strategies differed. In the smaller regional and community sites, cancer patient navigators (CPNs) were available for complex distress management. In the larger tertiary cancer centers where the CPN role is not part of the care model, psychologists and social workers were available to assist with complex distress management.

As per the QI methodology, the approach for implementing the SFD intervention included Plan, Do, Study, Act (PDSA) cycles to optimize the process.34 Chart audits were used to drive PDSA cycles and gauge effectiveness of ongoing QI efforts. Upon request from sites, 2- to 3-hour booster education sessions were conducted.

Cohort 2: Ten months after implementation, HCPs were asked to complete the same anonymous questionnaire used with cohort 1. This occurred between August 2013 and June 2014. No controls were taken to manage which HPCs participated in either cohort.

This project was conducted in compliance with the Helsinki Declaration and the Alberta Research Ethics Community Consensus Initiative (ARECCI)35 ethical guidelines for QI and evaluation. After screening with the ethical principles established by ARECCI, full Research Ethics Board review was waived. No harm was anticipated or actually reported in relation to this project.

Measures

Confidence in Assessing and Managing Distress: This tool was developed to measure HCP's confidence in assessing and managing patient distress after the completion of a Web-based education program for SFD.33 One additional item was added to assess the level of confidence in referring patients to outside agencies. The revised 12-item scale confirmed the original one-factor structure. The internal consistency (Cronbach's alpha) was 0.92. Respondents were asked to indicate to what extent each statement applies to them on a 5-point Likert scale ranging from “not confident at all” to “extremely confident.” A total score was created by summing the 12 scores.

The Person-Centered Care Assessment Tool: The Person-Centered Care Assessment Tool (P-CAT) was originally developed to measure perception of person-centeredness for geriatric care settings.36 One item not relevant to cancer was excluded. Factor analyses for the revised 12-item scale confirmed the original 3-factor structure. The internal consistency (Cronbach's alpha) was 0.85. Participants were asked to indicate to what extent they agreed with each statement on a 5-point Likert scale ranging from “disagree completely” to “agree completely.” A total score was created by summing the 12 scores.

Post-Implementation Evaluations

HCPs in cohort 2 were asked 4 additional questions, including an assessment of the usefulness of SFD, the extent to which screening might cause a delay in clinic visits, and whether they experienced positive or negative impacts of SFD.

Chart Reviews for Ongoing QI

Medical charts were randomly reviewed by project coordinators at midpoint and the end of the implementation period at all sites. The percentages of patients screened, tool reviewed, conversations documented, and actions taken were recorded to direct further improvements.

Statistical Analyses

Normality was assessed for the distribution of the outcome measures. Chi-square tests were used to compare the 2 cohorts in the binary/categorical variables for occupations, tumor groups (single or multiple), and locations. In order to assess the main effect of the intervention, independent t-tests were conducted to compare staff's confidence level and awareness in person-centeredness between the cohorts. In order to assess the potential impacts of different models of care, t-tests were conducted to compare confidence and awareness levels in staff at tertiary and regional/community sites within each cohort. When significant differences between sites within each cohort were found, a regression analysis was performed to examine whether the differences between sites before the intervention was significantly different from the differences after the intervention (cohort × site interaction). Additional sensitivity analyses were included to address potential selection bias, effect modification, or confounding effects related to pre- and post-intervention differences in the proportion of respondents treating single versus multiple tumors. Chi-square tests were used for analyses of post-implementation evaluations. All statistical analyses were performed with SPSS version 21.

Results

Participants

Table 1 represents participant characteristics. Cohort 1 included 254 HCPs, whereas cohort 2 included 158. The 2 cohorts were well-balanced in their occupations and clinic locations; however, significantly fewer staff in cohort 2 cared for single tumors relative to staff in cohort 1 (χ2[N=412], 45.39; P<.001).

Validation of Program Implementation

The SFD intervention was adopted and routinely conducted. The provincial-average screening rate reached 94.6%. The average rate of follow-up assessments or referral related to the SFD intervention reached 68.8%.

Comparisons Between Cohorts: Pre- and Post-Intervention

Cohort 2 staff reported significantly greater confidence in managing and assessing patient distress (mean, 37.88; SD, 9.36) relative to cohort 1 staff (mean, 35.89; SD, 8.80), [t(357), −2.05; P=.041; mean difference, −1.99; 95% CI, −3.90 to −0.08]. Similarly, cohort 2 staff reported significantly greater awareness in person-centeredness (mean, 46.70; SD, 6.09) relative to cohort 1 staff (mean, 44.48; SD, 6.65), [t(381), −3.31; P=.001; mean difference, −2.22; 95% CI, −3.54 to −0.90]. Figure 1 represents the mean confidence scores, and Figure 2 represents the mean awareness scores for each cohort.

Comparisons Between Sites: Models of Care and Sensitivity Analyses

In cohort 1, staff at tertiary and regional/community sites were similar in their levels of confidence in assessing distress [t(210), 0.27; P=.738]. However, staff at regional/community sites reported greater awareness in person-centeredness relative to staff at tertiary sites [t(227), −2.39; P=.018]. Similarly, in cohort 2, no differences were found between staff at tertiary and regional/community sites in the levels of confidence [t(144), 0.26; P=.798]. However, staff at regional/community clinics reported significantly greater awareness in person-centeredness relative to staff at tertiary sites following the implementation of SFD [t(151), −3.67; P<.001]. Regression analyses showed no significant interaction effect between cohort and site for the awareness (B: 1.37; 95% CI, −1.24–3.97; P=.303), indicating the difference in awareness between sites was similar before and after the intervention. Figure 3 shows mean confidence scores, and Figure 4 represents mean awareness scores for each site and cohort. Table 2 summarizes means and SDs for the outcomes for each site and cohort.

As reported earlier, fewer respondents treated single tumors in cohort 2 relative to cohort 1. Similarly, fewer HCPs at regional/community sites cared for single tumors (20%) relative to HCPs at tertiary sites (40%). Therefore, a sensitivity analysis was conducted by selecting only those who treat single tumors and those who treat multiple tumors. The

Table 1.

Background Characteristics of Staff Members

Table 1.
differences in both confidence and awareness between cohorts, and the difference in awareness between sites were verified only for HCPs who treat multiple tumors. Table 3 is a 3-way table (Cohort × site × single/multiple tumors) indicating caring for single or multiple tumors is an effect modifier.

Figure 1.
Figure 1.

Mean scores of confidence in assessing and managing patients' distress for cohorts 1 and 2.

Citation: Journal of the National Comprehensive Cancer Network J Natl Compr Canc Netw 14, 10; 10.6004/jnccn.2016.0135

Figure 2.
Figure 2.

Mean scores of awareness of person-centered care for cohorts 1 and 2.

Citation: Journal of the National Comprehensive Cancer Network J Natl Compr Canc Netw 14, 10; 10.6004/jnccn.2016.0135

Post-Implementation Evaluations

Most staff evaluated the SFD intervention either very helpful (22.2%) or somewhat helpful (49.4%) as opposed to not at all helpful (17.7%). Staff variously rated the length of delay in patient appointment times caused by screening; no delay (30.4%), 1 to 2 minutes (7.6%), 5 to 10 minutes (18.4%), and more than 10 minutes delay (26.0%). Most commonly endorsed positive impacts were “SFD was useful to get more comprehensive picture of how the patient is doing” (44.3%), and “SFD allowed more focused assessment” (38.0%). Most often-endorsed negative effects were “Too time-consuming” (31.0%), and “Extra details not relevant to care” (22.2%).

Staff at tertiary and regional/community sites were similar in their evaluation of the usefulness of SFD (χ2[N=140], 5.41; P=.067) and the extent to which screening caused a delay in patients' appointment times (χ2[N=129], 0.15; P=.928). Staff at tertiary and regional/community sites endorsed positive impacts of SFD in a similar manner; however, significantly more staff at tertiary sites (29.5%) endorsed “SFD addressed extra details not relevant to care” relative to those at regional/community sites (13.9%) (χ2[N=157], 5.60; P=.018). There was a statistical trend that more staff at tertiary sites (38.5%) endorsed “Too time-consuming” (χ2[N=157], 3.80; P=.051) relative to staff at regional/community sites (24.1%). Figures 5 and 6 illustrate the positive and negative impacts of SFD, respectively.

Discussion

This evaluation examined HCPs perceptions of the impact of a provincial QI project aimed at integrating the SFD intervention into routine cancer care.

Figure 3.
Figure 3.

Mean scores of confidence in assessing and managing patients' distress for tertiary sites and regional/community cancer center (RCC/CCC) sites within each cohort.

Citation: Journal of the National Comprehensive Cancer Network J Natl Compr Canc Netw 14, 10; 10.6004/jnccn.2016.0135

Figure 4.
Figure 4.

Mean scores of awareness of person-centered care for tertiary sites and regional/community cancer center (RCC/CCC) sites within each cohort.

Citation: Journal of the National Comprehensive Cancer Network J Natl Compr Canc Netw 14, 10; 10.6004/jnccn.2016.0135

Table 2.

Means and SDs for Outcome Measures at Tertiary and Regional/Community Sites in Each Cohort

Table 2.
This evaluation demonstrated higher levels of confidence in assessing and managing patient distress and awareness of person-centeredness among HCPs who were part of the SFD intervention relative to HCPs who were not exposed to the intervention. To our knowledge, this is the first study to document the direct benefits of comprehensive implementation strategy on HCPs' confidence in assessing and managing distress and their perceptions regarding the extent to which their care delivery is person-centered. Importantly, these benefits were found regardless of models of care or facility types across the province.

The observed benefits can be explained by efficacious use of clinical resources in this project. Some distressing conditions are best managed by physicians, such as pain, whereas other issues are best managed by other members of the interdisciplinary team. Given previously identified barriers for accurately detecting patients' distress,1012,19,23 this project assigned other HCPs to conduct the initial distress assessment. The observed improvement in HCPs' confidence levels and awareness in person-centeredness shows that the SFD intervention can build interdisciplinary teams' competency while physicians can remain more focused on issues that must be managed by a physician.

In line with previous work,16,2729 most of the HCPs in this study valued the addition of the SFD intervention in their practice. The most often endorsed positive impact was that staff saw a more comprehensive picture of their patients (44%), aligning with HCPs' evaluation from a different provincial cancer agency's initiative.29 The current project reached more than a 90% screening rate, with a satisfactory level of follow-up (69%). This result was

Table 3.

Means and SDs for Outcome Measures Among HCPs Caring for Single and Multiple Tumor Groups at Tertiary and Regional/Community Sites in Each Cohort

Table 3.
Figure 5.
Figure 5.

Positive impacts of screening for distress.

Citation: Journal of the National Comprehensive Cancer Network J Natl Compr Canc Netw 14, 10; 10.6004/jnccn.2016.0135

enabled through the comprehensive QI approach, which included education, process change, and ongoing PDSA cycles. In particular, staff education played a significant role in the philosophical buyin of person-centeredness. We believe this practice change has enhanced the clinical team's ability to manage patient's distress and provide person-centered care more consistently. “Too time-consuming” was the most commonly endorsed negative impact of SFD (31%), highlighting time constraints as a barrier to screening.19,23,25 Future QI work is needed to identify the cause of the delay and to implement electronic screening tools to minimize time impact.

A greater awareness in person-centeredness was found among staff at regional/community sites relative to staff at tertiary sites before and after SFD implementation. This is rather expected given that the patient–provider interaction tends to be more personal at smaller care facilities. However, no significant interaction effect between cohort and site suggests that similar benefits were found after implementation at all sites. This study identified caring for single or multiple tumors as an effect modifier, with effects observed in the HCPs treating multiple tumors, but not HCPs treating single tumors. We presented the group-specific effects because the average effect would be misleading as the effects differ between HCPs treating single and multiple tumors. This may reflect different models of care in actual clinical settings. At tertiary sites, tumor-specific care can be provided, whereas at smaller sites, most HCPs take a generalist model of

Figure 6.
Figure 6.

Negative impacts of screening for distress.

*P<.050.

Citation: Journal of the National Comprehensive Cancer Network J Natl Compr Canc Netw 14, 10; 10.6004/jnccn.2016.0135

care and treat various cancer types. The results demonstrate the importance of taking into account factors intrinsic to existing care models.

Fewer staff at sites with a CPN endorsed the negative impacts of SFD, suggesting that navigators significantly ease staff burden related to managing distress. At tertiary sites where navigators were not available, more staff felt that SFD introduced issues that were outside of their perceived scope of responsibility. Future work involving staff education regarding the pervasive influence of distress on patients and cancer care, and the benefits of SFD is required. Given the benefits found in this evaluation, integrating the SFD intervention into clinical environments where navigators are available may be an ideal model.37,38 It also enhances the feasibility of distress management within community settings where supportive care resources are limited.22

This study had some limitations. We did not use a control group or follow the same group of individuals before and after the implementation; hence, this evaluation does not allow comment on cause-and-effect relationships. However, the current design was more suited for this pragmatic study in which the SFD intervention was implemented within the existing clinical environment. The self-selected nature of the study might result in the unbalance of HCPs treating single and multiple tumors between the cohorts and facility types, representing a risk of selection bias. Analytically, we could not deny this risk because of the small number of HCPs who treated single tumors in cohort 2. Previous studies highlight a more positive attitude toward routine screening among nurses and allied HCPs relative to physicians.29,39 Most of our participants were nurses (61.2% in cohort 1; 57.6% in cohort 2). Therefore, our results may not be generalizable to other HCPs. Building on this work, future research to evaluate the sustainability of the SFD intervention as a standard of care would be valuable.

Acknowledgments

The authors would like to thank all of the healthcare professionals who participated in this evaluation.

The authors have disclosed that they have no financial interests, arrangements, affiliations, or commercial interests with the manufacturers of any products discussed in this article or their competitors. This work was supported by Alberta Cancer Foundation, Grant number 25984.

References

  • 1

    Bultz BD, Holland JC. Emotional distress in patients with cancer: the sixth vital sign. J Psychosoc Oncol 2006;3:311314.

  • 2

    Carlson LE, Groff SL, Maciejewski O, Bultz BD. Screening for distress in lung and breast cancer outpatients: a randomized controlled trial. J Clin Oncol 2010;28:48844891.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 3

    Chambers SK, Zajdlewicz L, Youlden DR et al.. The validity of the distress thermometer in prostate cancer populations. Psychooncology 2014;23:195203.

  • 4

    Mitchell AJ, Chan M, Bhatti H et al.. Prevalence of depression, anxiety, and adjustment disorder in oncological, haematological, and palliative-care settings: a meta-analysis of 94 interview-based studies. Lancet Oncol 2011;12:160174.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 5

    Holland JC, Jacobsen PB, Andersen B et al.. NCCN Clinical Practice Guidelines in Oncology: Distress Management. Version 2.2016. To view the most recent version of these guidelines, visit NCCN.org.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 6

    Kirkova J, Walsh D, Rybicki L et al.. Symptom severity and distress in advanced cancer. Palliat Med 2010;24:330339.

  • 7

    Waller A, Groff SL, Hagen N et al.. Characterizing distress, the 6th vital sign, in an oncology pain clinic. Curr Oncol 2012;19:e5359.

  • 8

    Von Essen L, Larsson G, Oberg K, Sjoden PO. Satisfaction with care: associations with health-related quality of life and psychosocial function among Swedish patients with endocrine gastrointestinal tumors. Eur J Cancer Care 2002;11:9199.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 9

    Keller M, Sommerfeldt S, Fischer C et al.. Recognition of distress and psychiatric morbidity in cancer patients: a multi-method approach. Ann Oncol 2004;15:12431249.

  • 10

    Fallowfield L, Ratcliffe D, Jenkins V, Saul J. Psychiatric morbidity and its recognition by doctors in patients with cancer. Br J Cancer 2001;84:10111015.

  • 11

    Werner A, Stenner C, Schuz J. Patient versus clinician symptom reporting: how accurate is the detection of distress in the oncologic after-care? Psychooncology 2012;21:818826.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 12

    Mitchell AJ, Kaar S, Coggan C, Herdman J. Acceptability of common screening methods used to detect distress and related mood disorders – preferences of cancer specialists and non-specialists. Psychooncology 2008;17:226236.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 13

    Accreditation Canada. Qmentum Program 2009. Standards. Cancer care and oncology services. Version 2. Available at: https://www3.accreditation.ca/SurveyorPortal/DOCUMENTS/AccProgram/2009/en-CA/CCO.pdf. Accessed January 6, 2016.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 14

    Bultz B, Johansen C. Screening for distress, the 6th vital sign: where are we, and where are we going? Psychooncology 2011;20:569571.

  • 15

    Canadian Partnership Against Cancer. Cancer Journey Portfolio. Screening for Distress, the 6th Vital Sign: A Guide to Implementing Best Practices in Person-Centred Care. Available at: www.cancerview.ca/idc/groups/public/documents/webcontent/guide_implement_sfd.pdf. Accessed January 6, 2016.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 16

    Berry DL, Blumenstein BA, Halpenny B et al.. Enhancing patient-provider communication with the electronic self-report assessment for cancer: a randomised trial. J Clin Oncol 2011;29:10291035.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 17

    Barbera L, Sutradhar R, Howell D et al.. Does routine symptom screening with ESAS decrease ED visits in breast cancer patients undergoing adjuvant chemotherapy? Support Care Cancer 2015;23:30253032.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 18

    Pereira J, Macdougall L, Green E et al.. Population-based standardized symptom screening: Cancer Care Ontario's Edmonton Symptom Assessment System and performance status initiatives. J Oncol Pract 2014;10:212214.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 19

    Mitchell AJ. Screening for cancer-related distress: when is implementation successful and when is it unsuccessful? Acta Oncol 2013;52:216.

  • 20

    Carlson LE, Waller A, Mitchell AJ. Screening for distress and unmet needs in patients with cancer: review and recommendations. J Clin Oncol 2012;30:1160.

  • 21

    Breaken AP, Kempen GI, Eekers D et al.. The usefulness and feasibility of a screening instrument to identify psychosocial problems in patients receiving curative radiotherapy: a process evaluation. BMC Cancer 2011;11:479.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 22

    Gilbert JE, Howell D, King S et al.. Quality improvement in cancer symptom assessment and control: the provincial palliative care integration project (PPCIP). J Pain Symptom Manage 2012;43:663678.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 23

    Chiang AC, Buia Amport S, Corjulo D et al.. Incorporating patient-reported outcomes to improve emotional distress screening and assessment in an ambulatory oncology clinic. J Oncol Pract 2015;11:219222.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 24

    Absolom K, Holch P, Pini S et al.. The detection and management of emotional distress in cancer patients: the views of health-care professionals. Psychooncology 2011;20:601608.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 25

    Howell D, Molloy S, Wilkinson K et al.. Patient-reported outcomes in routine cancer clinical practice: a scoping review of use, impact on health outcomes, and implementation factors. Ann Oncol 2015;26:18461858.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 26

    Dilworth S, Higgins I, Parker V et al.. Patient and health professional's perceived barriers to the delivery of psychosocial care to adults with cancer: a systematic review. Psychooncology 2014;23:601612.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 27

    Kallen MA, Yang D, Haas N. A technical solution to improving palliative and hospice care. Support Care Cancer 2012;20:167174

  • 28

    Snyder C, Blackford A, Wolff A et al.. Feasibility and value of patient-viewpoint: a web system for patient-reported outcomes assessment in clinical practice. Psychooncology 2013;22:895901.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 29

    Pereira JL, Chasen MR, Molloy S et al.. Cancer care professionals' attitudes toward systematic standardized symptom assessment and the Edmonton Symptom Assessment System (ESAS) following large-scale population-based implementation in Ontario, Canada. J Pain Symptom Manage 2016;51:662672.e8.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 30

    Watson L, Groff S, Tamagawa R et al.. Implementation of screening for distress on quality of life, symptom reports, and psychosocial well-being in patients with cancer. J Natl Compr Canc Netw 2016;14:164172.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 31

    Bruera E, Kuehn N, Miller MJ et al.. The Edmonton Symptom Assessment System (ESAS): a simple method for the assessment of palliative care patients. J Palliat Care 1991;7:69.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 32

    Canadian Partnership Against Cancer. Guide to Implementing Screening for Distress, the 6th Vital Sign. Part A: Background, Recommendations, and Implementation. Available at: https://www.gem-measures.org/Public/DownloadDocument.aspx?LinkID=71. Accessed January 6, 2016.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 33

    IPODE Project. Canadian Association of Psychosocial Oncology Website. Available at: http://www.capo.ca/ipode-project/screening-for-distress/. Accessed August 28, 2014.

    • PubMed
    • Export Citation
  • 34

    Langley GL, Nolan KM, Norman CL, Provost LP. The Improvement Guide: A Practical Approach to Enhancing Organizational Performance, 2nd ed. San Francisco, CA: Jossey-Bass Publishers; 2009.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 35

    ARECCI: A Project Ethics Community Consensus Initiative. Alberta Innovates Health Solutions Web site. Available at: http://www.aihealthsolutions.ca/initiatives-partnerships/arecci-a-project-ethics-community-consensus-initiative/. Accessed May 11, 2015.

    • PubMed
    • Export Citation
  • 36

    Edvardsson D, Fetherstonhaugh D, Nav R, Gibson S. Development and initial testing of the person-centred care assessment tool (P-CAT). Int Psychogeriatr 2010;22:101108.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 37

    Weber JJ, Mascarenhas DC, Bellin LS et al.. Patient navigation and the quality of breast cancer care: an analysis of the breast cancer care quality indicators. Ann Surg Oncol 2012;19:32513256.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 38

    Campbell C, Craig J, Eggert J, Bailey-Dorton C. Implementing and measuring the impact of patient navigation at a comprehensive community cancer center. Oncol Nurs Forum 2010;37:6168.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 39

    Bainbridge D, Seow H, Sussman J et al.. Multidisciplinary health care professionals' perceptions of the use and utility of a symptom assessment system for oncology patients. J Oncol Pract 2011;7:1923.

    • PubMed
    • Search Google Scholar
    • Export Citation

Author Contributions: Project evaluation, data analyses, literature review, and lead manuscript writer: Tamagawa. Project coordinator and prepared a grant application for the study: Groff. Assisted program coordination and staff education at different sites: Anderson and Champ. Program assistant and administration: Deiure. Literature review and manuscript writing: Looyis. Principal investigator, recipient of a grant for the study, and manuscript writing: Watson.

Correspondence: Linda Watson, PhD, RN, Person-Centered Care Integration, CancerControl Alberta, Alberta Health Services, Tom Baker Cancer Center, Holy Cross Site, 2202 2nd Street SW, Calgary, AB, T2S 3C1, Canada. E-mail: linda.watson@albertahealthservices.ca
  • Collapse
  • Expand
  • Mean scores of confidence in assessing and managing patients' distress for cohorts 1 and 2.

  • Mean scores of awareness of person-centered care for cohorts 1 and 2.

  • Mean scores of confidence in assessing and managing patients' distress for tertiary sites and regional/community cancer center (RCC/CCC) sites within each cohort.

  • Mean scores of awareness of person-centered care for tertiary sites and regional/community cancer center (RCC/CCC) sites within each cohort.

  • Positive impacts of screening for distress.

  • Negative impacts of screening for distress.

    *P<.050.

  • 1

    Bultz BD, Holland JC. Emotional distress in patients with cancer: the sixth vital sign. J Psychosoc Oncol 2006;3:311314.

  • 2

    Carlson LE, Groff SL, Maciejewski O, Bultz BD. Screening for distress in lung and breast cancer outpatients: a randomized controlled trial. J Clin Oncol 2010;28:48844891.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 3

    Chambers SK, Zajdlewicz L, Youlden DR et al.. The validity of the distress thermometer in prostate cancer populations. Psychooncology 2014;23:195203.

  • 4

    Mitchell AJ, Chan M, Bhatti H et al.. Prevalence of depression, anxiety, and adjustment disorder in oncological, haematological, and palliative-care settings: a meta-analysis of 94 interview-based studies. Lancet Oncol 2011;12:160174.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 5

    Holland JC, Jacobsen PB, Andersen B et al.. NCCN Clinical Practice Guidelines in Oncology: Distress Management. Version 2.2016. To view the most recent version of these guidelines, visit NCCN.org.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 6

    Kirkova J, Walsh D, Rybicki L et al.. Symptom severity and distress in advanced cancer. Palliat Med 2010;24:330339.

  • 7

    Waller A, Groff SL, Hagen N et al.. Characterizing distress, the 6th vital sign, in an oncology pain clinic. Curr Oncol 2012;19:e5359.

  • 8

    Von Essen L, Larsson G, Oberg K, Sjoden PO. Satisfaction with care: associations with health-related quality of life and psychosocial function among Swedish patients with endocrine gastrointestinal tumors. Eur J Cancer Care 2002;11:9199.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 9

    Keller M, Sommerfeldt S, Fischer C et al.. Recognition of distress and psychiatric morbidity in cancer patients: a multi-method approach. Ann Oncol 2004;15:12431249.

  • 10

    Fallowfield L, Ratcliffe D, Jenkins V, Saul J. Psychiatric morbidity and its recognition by doctors in patients with cancer. Br J Cancer 2001;84:10111015.

  • 11

    Werner A, Stenner C, Schuz J. Patient versus clinician symptom reporting: how accurate is the detection of distress in the oncologic after-care? Psychooncology 2012;21:818826.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 12

    Mitchell AJ, Kaar S, Coggan C, Herdman J. Acceptability of common screening methods used to detect distress and related mood disorders – preferences of cancer specialists and non-specialists. Psychooncology 2008;17:226236.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 13

    Accreditation Canada. Qmentum Program 2009. Standards. Cancer care and oncology services. Version 2. Available at: https://www3.accreditation.ca/SurveyorPortal/DOCUMENTS/AccProgram/2009/en-CA/CCO.pdf. Accessed January 6, 2016.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 14

    Bultz B, Johansen C. Screening for distress, the 6th vital sign: where are we, and where are we going? Psychooncology 2011;20:569571.

  • 15

    Canadian Partnership Against Cancer. Cancer Journey Portfolio. Screening for Distress, the 6th Vital Sign: A Guide to Implementing Best Practices in Person-Centred Care. Available at: www.cancerview.ca/idc/groups/public/documents/webcontent/guide_implement_sfd.pdf. Accessed January 6, 2016.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 16

    Berry DL, Blumenstein BA, Halpenny B et al.. Enhancing patient-provider communication with the electronic self-report assessment for cancer: a randomised trial. J Clin Oncol 2011;29:10291035.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 17

    Barbera L, Sutradhar R, Howell D et al.. Does routine symptom screening with ESAS decrease ED visits in breast cancer patients undergoing adjuvant chemotherapy? Support Care Cancer 2015;23:30253032.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 18

    Pereira J, Macdougall L, Green E et al.. Population-based standardized symptom screening: Cancer Care Ontario's Edmonton Symptom Assessment System and performance status initiatives. J Oncol Pract 2014;10:212214.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 19

    Mitchell AJ. Screening for cancer-related distress: when is implementation successful and when is it unsuccessful? Acta Oncol 2013;52:216.

  • 20

    Carlson LE, Waller A, Mitchell AJ. Screening for distress and unmet needs in patients with cancer: review and recommendations. J Clin Oncol 2012;30:1160.

  • 21

    Breaken AP, Kempen GI, Eekers D et al.. The usefulness and feasibility of a screening instrument to identify psychosocial problems in patients receiving curative radiotherapy: a process evaluation. BMC Cancer 2011;11:479.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 22

    Gilbert JE, Howell D, King S et al.. Quality improvement in cancer symptom assessment and control: the provincial palliative care integration project (PPCIP). J Pain Symptom Manage 2012;43:663678.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 23

    Chiang AC, Buia Amport S, Corjulo D et al.. Incorporating patient-reported outcomes to improve emotional distress screening and assessment in an ambulatory oncology clinic. J Oncol Pract 2015;11:219222.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 24

    Absolom K, Holch P, Pini S et al.. The detection and management of emotional distress in cancer patients: the views of health-care professionals. Psychooncology 2011;20:601608.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 25

    Howell D, Molloy S, Wilkinson K et al.. Patient-reported outcomes in routine cancer clinical practice: a scoping review of use, impact on health outcomes, and implementation factors. Ann Oncol 2015;26:18461858.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 26

    Dilworth S, Higgins I, Parker V et al.. Patient and health professional's perceived barriers to the delivery of psychosocial care to adults with cancer: a systematic review. Psychooncology 2014;23:601612.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 27

    Kallen MA, Yang D, Haas N. A technical solution to improving palliative and hospice care. Support Care Cancer 2012;20:167174

  • 28

    Snyder C, Blackford A, Wolff A et al.. Feasibility and value of patient-viewpoint: a web system for patient-reported outcomes assessment in clinical practice. Psychooncology 2013;22:895901.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 29

    Pereira JL, Chasen MR, Molloy S et al.. Cancer care professionals' attitudes toward systematic standardized symptom assessment and the Edmonton Symptom Assessment System (ESAS) following large-scale population-based implementation in Ontario, Canada. J Pain Symptom Manage 2016;51:662672.e8.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 30

    Watson L, Groff S, Tamagawa R et al.. Implementation of screening for distress on quality of life, symptom reports, and psychosocial well-being in patients with cancer. J Natl Compr Canc Netw 2016;14:164172.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 31

    Bruera E, Kuehn N, Miller MJ et al.. The Edmonton Symptom Assessment System (ESAS): a simple method for the assessment of palliative care patients. J Palliat Care 1991;7:69.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 32

    Canadian Partnership Against Cancer. Guide to Implementing Screening for Distress, the 6th Vital Sign. Part A: Background, Recommendations, and Implementation. Available at: https://www.gem-measures.org/Public/DownloadDocument.aspx?LinkID=71. Accessed January 6, 2016.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 33

    IPODE Project. Canadian Association of Psychosocial Oncology Website. Available at: http://www.capo.ca/ipode-project/screening-for-distress/. Accessed August 28, 2014.

    • PubMed
    • Export Citation
  • 34

    Langley GL, Nolan KM, Norman CL, Provost LP. The Improvement Guide: A Practical Approach to Enhancing Organizational Performance, 2nd ed. San Francisco, CA: Jossey-Bass Publishers; 2009.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 35

    ARECCI: A Project Ethics Community Consensus Initiative. Alberta Innovates Health Solutions Web site. Available at: http://www.aihealthsolutions.ca/initiatives-partnerships/arecci-a-project-ethics-community-consensus-initiative/. Accessed May 11, 2015.

    • PubMed
    • Export Citation
  • 36

    Edvardsson D, Fetherstonhaugh D, Nav R, Gibson S. Development and initial testing of the person-centred care assessment tool (P-CAT). Int Psychogeriatr 2010;22:101108.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 37

    Weber JJ, Mascarenhas DC, Bellin LS et al.. Patient navigation and the quality of breast cancer care: an analysis of the breast cancer care quality indicators. Ann Surg Oncol 2012;19:32513256.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 38

    Campbell C, Craig J, Eggert J, Bailey-Dorton C. Implementing and measuring the impact of patient navigation at a comprehensive community cancer center. Oncol Nurs Forum 2010;37:6168.

    • PubMed
    • Search Google Scholar
    • Export Citation
  • 39

    Bainbridge D, Seow H, Sussman J et al.. Multidisciplinary health care professionals' perceptions of the use and utility of a symptom assessment system for oncology patients. J Oncol Pract 2011;7:1923.

    • PubMed
    • Search Google Scholar
    • Export Citation
All Time Past Year Past 30 Days
Abstract Views 0 0 0
Full Text Views 582 99 5
PDF Downloads 208 47 5
EPUB Downloads 0 0 0