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Barriers and facilitators to implementing the commission on cancer's distress screening program standard

Published online by Cambridge University Press:  08 June 2018

Andrea K. Knies ,
Devika R. Jutagir Open the ORCID record for Devika R. Jutagir [Opens in a new window] ,
Elizabeth Ercolano ,
Nicholas Pasacreta ,
Mark Lazenby  and
Ruth McCorkle
Andrea K. Knies*
Affiliation:
Yale University School of Nursing, West Haven, CT
Devika R. Jutagir
Affiliation:
Yale University School of Medicine, New Haven, CT
Elizabeth Ercolano
Affiliation:
Yale University School of Nursing, West Haven, CT
Nicholas Pasacreta
Affiliation:
Yale University School of Nursing, West Haven, CT
Mark Lazenby
Affiliation:
Yale University School of Nursing, West Haven, CT
Ruth McCorkle
Affiliation:
Yale University School of Nursing, West Haven, CT
*
Author of correspondence: Andrea K. Knies, Department of Neurology, Division of Neurocritical Care & Emergency Medicine, Yale School of Medicine, 15 York Street, New Haven, CT 06510. E-mail: [email protected]
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Abstract

Objective

Many cancer centers struggle to implement standardized distress screening despite the American College of Surgeons’ Commission on Cancer 2012 mandate for a distress screening program standard of care by 2015. This paper presents outcomes for the first cohort of participants (n = 36) of a Screening for Psychosocial Distress Program (SPDP), a 2-year training program designed to assist clinicians in implementing routine distress screening as mandated by the American College of Surgeons Commission on Cancer. Specifically, participants’ success with distress screening implementation, institutional barriers and facilitators to implementation, and the role of the SPDP are described.

Method

This research followed a longitudinal pre- and posttest mixed methods design. An investigator-developed questionnaire collected qualitative (distress screening goals, institutional barriers and facilitators, facilitators associated with participation in the SPDP) and quantitative (level of goal achievement) data at 6, 12, and 24 months of participation in the SPDP. Conventional content analysis was applied to qualitative data. Mixed methods data analysis in Dedoose evaluated (1) types and number of distress screening goals, barriers, and facilitators, and (2) goal achievement at 6, 12, and 24 months of participation.

Result

Ninety-five percent of distress screening implementation goals were completed after 2 years of participation. Most common institutional barriers to distress screening implementation were “lack of staff,” “competing demands,” and “staff turn-over.” Most common institutional facilitators were “buy-in,” “institutional support,” and “recognition of participants’ expertise.” The number of reported facilitators associated with SPDP participation was higher than the number associated with any institutional factor, and increased over time of participation.

Significance of results

Participating in training programs to implement distress screening may facilitate successful achievement of the Commission on Cancer's distress screening standard, and benefits seem to increase with time of participation. Training programs are needed to promote facilitators and overcome barriers to distress screening.

Keywords

Quality of lifedistress screeningcanceranxiety/depressioninterventions
Type
Original Article
Information
Palliative & Supportive Care , Volume 17 , Issue 3 , June 2019 , pp. 253 - 261
Copyright
Copyright © Cambridge University Press 2018 

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Footnotes

*

These authors shared first authorship.

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