Canadian Association of Psychosocial Oncology
Association Canadienne d'Oncologie Psychosociale
National Psychosocial Oncology Standards

National Psychosocial Oncology Standards for Canada

July 9, 1999 (Board Approved September, 1999)


TABLES OF CONTENTS

Section I - INTRODUCTION

Section II - DEFINITION OF PSYCHOSOCIAL ONCOLOGY and SCOPE OF STANDARDS

Section III - PRINCIPLES OF PRACTICE IN PSYCHOSOCIAL ONCOLOG

PRINCIPLE 1 - Integral Part of Care
PRINCIPLE 2 - Patient/Family Focus of Care
PRINCIPLE 3 - Access to Psychosocial Care
PRINCIPLE 4 - Focus of Psychosocial Care
PRINCIPLE 5 - Respect
PRINCIPLE 6 - Ethical Practice
PRINCIPLE 7 - Assessment of Need
PRINCIPLE 8 - Interdisciplinary Respect
PRINCIPLE 9 - Evidence Based Practice
PRINCIPLE 10 - Education and Research
PRINCIPLE 11 - Quality Improvement

Section IVA - ORGANIZATION AND STRUCTURE IN PSYCHOSOCIAL ONCOLOGY PROGRAMS

STANDARD 1 - Organizations will provide psychosocial care
STANDARD 2 - Psychosocial Oncology Program
STANDARD 3 - Program Resources
STANDARD 4 - Continuity of care
STANDARD 5 - Program Workload Data
STANDARD 6 - Represented in Administrative Structure
STANDARD 7 - Integrated Documentation
STANDARD 8 - Diversity
STANDARD 9 - Psychosocial Program Leadership

Section IVB - PROFESSIONAL ISSUES IN PSYCHOSOCIAL ONCOLOGY

STANDARD 10 - Professional Codes of Ethics
STANDARD 11 - Accountability for Qualifications
STANDARD 12 - Position Profile
STANDARD 13 - Qualifications of Staff
STANDARD 14 - Plan to Upgrade Qualifications
STANDARD 15 - Supervision
STANDARD 16 - Performance Reviews
STANDARD 17 - Regular Meetings
STANDARD 18 - Translating Research into Practice

Section IVC - PATIENT AND FAMILY SERVICE IN PSYCHOSOCIAL ONCOLOGY

STANDARD 19 - Information
STANDARD 20 - Equitable Access of Services
STANDARD 21 - Appropriate Services are Available
STANDARD 22 - Informed Consent
STANDARD 23 - Advocacy
STANDARD 24 - Open Referral Policy

Section IVD - RESEARCH and PROGRAM EVALUATION STANDARDS FOR PSYCHOSOCIAL ONCOLOGY PROGRAMS

STANDARD 25 - Supportive Research Environment
STANDARD 26 -Psychosocial Program Evaluation
STANDARD 27 - Research and Ethics Review
STANDARD 28 - Research Resources Available

Section IVE - PATIENT AND STAFF EDUCATION IN PSYCHOSOCIAL ONCOLOGY

STANDARD 29 - Educational Needs Are Identified
STANDARD 30 - Educational Resources are Easily Accessible
STANDARD 31 - Relevance of Educational Material
STANDARD 32 - Continuing Professional Education
STANDARD 33 - Formal Evaluation of Educational Programs

REFERENCES

Appendix A

 

Section I - INTRODUCTION

The Canadian Association of Psychosocial Oncology (CAPO) is a professional organization, established in 1985, to bring together the disciplines which play a major role in the delivery of psychosocial services, research, and education in oncology. The goals of CAPO are:

  1. To provide a national network for the exchange of ideas between clinicians, researchers and educators.
  2. To actively foster and encourage interdisciplinary collaboration on oncology clinics and services.
  3. To establish and promote sound research and clinical practice guidelines.
  4. To promote and encourage psychosocial research
  5. To provide and promote ongoing education programs directed towards strengthening clinical service and research methodology.
  6. To promote and encourage multi-centre collaboration in clinical service, research and education.
  7. To offer advice and/or consultation services to members of the Association and to international, federal, provincial and local programs.

The National Standards for Psychosocial Oncology have been developed to assist cancer facilities, program leaders and practitioners in the delivery of psychosocial care in Canada by providing a basic framework for the practice of psychosocial oncology. This initiative came about from a recognition that psychosocial oncology standards are required to ensure that the basic principles and quality of care in the domain of psychosocial oncology are consistently applied and available to people living with cancer across Canada.

It is recognized that all health care disciplines provide some components of psychosocial oncology care through their day-to-day contact with patients and families. Indeed, a foundation of psychosocial oncology is the fundamental principle of an interdisciplinary area of expertise. These standards should not in any way detract from that basic principle and are not meant to restrain or limit the excellent psychosocial care and services being provided by various professional groups. They are intended to define the most basic and fundamental requirements of psychosocial oncology, upon which other professional groups, components, services and activities could, and even should, be added as required.

During the development of these standards comments were received about whether or not they conformed with existing practices or were "realistic". The Work Group struggled with the issues of existing practices and what is "realistic". In the final analysis, it was felt that standards are achievable objectives towards which people strive and not simply an affirmation of the status quo. By the same token, they are not seen as being an ideal. Instead, they reflect, based on existing evidence and extensive clinical and administrative experience, the minimum basic level of practice of patient care, education and research in psychosocial oncology.

Psychosocial oncology professionals in Canada are guided by discipline specific standards through professional associations, the accreditation process, or individual facility priorities. The CAPO Standards of Care have been developed to augment any existing professional standards and indications are that they do not conflict with existing professional standards.

 

Process for Standards Development

This project was initiated in November, 1997, with eight professionals from across Canada representing the major disciplines offering psychosocial care (Appendix A). The National Standards Group conducted its work between then and July, 1999. Three drafts were prepared before the fourth draft was distributed widely to members of CAPO, other psychosocial oncology practitioners, researchers, educators, cancer agencies, and others for input and comment. Replies were received from 65 individuals and organizations and their comments incorporated into a revised fifth draft. A final sixth draft was finalized on March 19 - 20, 1999 and submitted to the CAPO Board in May, 1999 for consideration and further action. The Board approved the Standards in principle at the May 12, 1999 Board Meeting, and also requested members of the Board to forward refinements in wording to the Work Group. This final set of Standards were completed in July, 1999 and approved by the CAPO Board in September, 1999.

Special mention is made of Terry Bunston, Ph.D. Dr. Bunston was a member of the Work Group from November, 1997 until her death on September 3, 1998. Her wisdom, insight, and commitment were greatly respected by the Work Group and her valued contributions are reflected throughout these Standards.

These Standards are divided into four sections. The first section is this Introduction. Section II provides a definition of psychosocial oncology and defines the scope of these standards. Section III identifies key principles guiding the development of these standards. Section IV are the specific Standards organized under the following headings; IV-A Organization and Structure, IV-B Professional Issues, IV-C Patient and Family Services, IV-D Research and Program Evaluation, and IV-E Patient and Professional Education in psychosocial oncology.

Section II - DEFINITION OF PSYCHOSOCIAL ONCOLOGY and SCOPE OF STANDARDS

 

DEFINITION OF PSYCHOSOCIAL ONCOLOGY

Psychosocial Oncology is a professional sub-specialty in oncology. The domain of psychosocial oncology includes the formal study, understanding and treatment of the social, psychological, emotional, spiritual, quality of life and functional aspects of cancer as applied across the cancer trajectory from prevention through bereavement. It seeks to develop and integrate new knowledge and techniques of the psychosocial and biomedical sciences as it relates to cancer care

 

SCOPE OF STANDARDS

Psychosocial oncology services exist in a variety of settings, including hospitals, comprehensive cancer centres, satellite clinics and multipurpose public health clinics in urban and rural communities throughout Canada. The psychosocial oncology standards apply to this range of oncology health care services for patients, their families and care-givers. The Psychosocial Oncology standards are designed to guide administrators and professionals in the development of psychosocial oncology services.

 

 

Section III - PRINCIPLES OF PRACTICE IN PSYCHOSOCIAL ONCOLOGY

 

PRINCIPLE 1 - Integral Part of Care

Psychosocial oncology is an integral part of cancer care.

 

PRINCIPLE - Patient/Family Focus of Care

The basic unit of care in psychosocial oncology is the patient and family, as defined by the patient.

 

PRINCIPE - Access to Psychosocial Care

Patients and families are informed of and have access to psychosocial oncology services.

 

PRINCIPLE 4 -Focus of Psychosocial Care

Psychosocial oncology aims to help individuals and families to use their own resources to promote well-being.

 

PRINCIPLE - Respect for Individual Integrity

Psychosocial Oncology professionals practice in a manner that respects the individuals' personal dignity and integrity.

 

PRINCIPLE 6 - Ethical Practice

Psychosocial Oncology professionals adhere to the ethical principles of autonomy, beneficence, honesty and confidentiality.

 

PRINCIPLE 7 - Assessment of Need

Psychosocial service needs of patients and families are assessed systematically using appropriate tools.

 

PRINCIPLE - Interdisciplinary Respect

The interdisciplinary team is built upon respect for each others’ expertise and knowledge base.

 

PRINCIPLE 9 - Evidence Based Practice

Psychosocial practice is evidence-based and subject to on-going evaluation.

 

PRINCIPLE 10 - Education and Research

Education and research are essential components of psychosocial oncology.

 

PRINCIPLE 11 Quality Improvement

Psychosocial oncology programs and services are subject to on-going quality improvement processes.

Section IVA - ORGANIZATION AND STRUCTURE IN PSYCHOSOCIAL ONCOLOGY PROGRAMS

Preamble

In recent years, there has been an increase in awareness of the burden of cancer carried by patients and their families. Adequate cancer care requires a comprehensive range of services that integrate psychosocial care. The organization must be structured in such a way that provides psychosocial resources to meet the needs of cancer patients and their support systems along the continuum from prevention to bereavement. It is recognized that some disciplines, by virtue of their particular formal training, must form the minimum requirement for a psychosocial oncology program. Yet, this does not detract from nor should it limit the excellent psychosocial care provide by many health care providers and anticipates that other disciplines, components, services and activities will, and in fact should, be part of the psychosocial oncology program. This could include professionals with appropriate psychosocial training from medicine, nursing, pastoral care or other related groups. It also recognizes that all health care disciplines provide some components of psychosocial care.

 

 

STANDARD 1 - Organizations will provide psychosocial care

Organizations caring for cancer patients must provide psychosocial care.

 

STANDARD 2 - Psychosocial Oncology Program

To be considered a psychosocial oncology program, at least 2 of the clinical disciplines of social work, psychology and/or psychiatry must provide psychosocial care and be present within the facility providing oncology care.

 

STANDARD 3 - Program Resources

The psychosocial oncology program maintains resources to provide clinical service and education and to conduct research.

 

STANDARD 4 - Continuity of care

Facilities providing cancer care ensure the continuity of psychosocial services for patients, and their families across the cancer continuum, with respect to the settings and providers.

 

STANDARD 5 Program Workload Data

The psychosocial oncology program collects data on patient care services, contacts and program delivery.

 

STANDARD 6 - Represented in Administrative Structure

Psychosocial services are represented in the administrative structures of the health care facility. Involvement in administration ensures direct input into resource allocations, integration of psychosocial services within program structures and accountability for psychosocial program evaluation and performance management.

 

STANDARD 7 - Integrated Documentation

Psychosocial professionals maintain complete and comprehensive records on patient encounters, which are consistent with discipline standards. These records are part of the official record maintained by the health care facility.

 

STANDARD 8 - Diversity

The diversity that characterizes the community where services are provided is reflected in the provision of psychosocial oncology services.

 

STANDARD 9 - Psychosocial Program Leadership

Leadership in psychosocial oncology comes from one of the three disciplines of social work, psychology or psychiatry. The leader is responsible for the development, evaluation and resource allocation of psychosocial programs and services within the cancer care facility.

Section IVB - PROFESSIONAL ISSUES IN PSYCHOSOCIAL ONCOLOGY

 

Preamble

Psychosocial Oncology functions within an interdisciplinary model of service delivery. Services are provided within a variety of organizational structures. Psychosocial oncology is an area of specialization, with few formal training opportunities. The purpose of this section is to ensure that psychosocial oncology professionals are qualified and trained, have relevant experience, and functions within a structure which supports their unique skills and expertise and ensures that they are able to maintain a high level of competence.

STANDARD 10 - Professional Codes of Ethics

Psychosocial oncology professionals adhere to their respective profession's Code of Ethics.

 

STANDARD 11 - Accountability for Qualifications

The psychosocial leader is responsible for ensuring that the qualifications and competencies of each professional within the psychosocial program are met.

STANDARD 12 - Position Profile

Qualifications and competencies (skill set) for professionals working in psychosocial oncology programs are defined in writing and are consistent with and augment provincial standards.

 

STANDARD 13 - Qualifications of Staff

Psychosocial oncology professionals will have

1) a graduate degree in social work, psychology, or psychiatry OR

2) at least 3 years supervised experience in psychosocial oncology post-Baccalaureate

 

STANDARD 14 - Plan to Upgrade Qualifications

A written plan is in place to ensure the qualifications/competencies will be achieved.

STANDARD 15 - Supervision

Professional staff with less than 3 years of psychosocial oncology experience will receive at least 4 hours/month of supervision/consultation until they achieve 3 years experience in psychosocial oncology. This can include one-to-one supervision, case discussions, research presentations, or other forms of consultation.

 

STANDARD 16 - Performance Reviews

Psychosocial oncology professionals meet annually with their immediate supervisor to review their work, performance, career and education plans, goals and objectives. A summary of that discussion is retained for reference and subsequent review.

 

STANDARD 17 - Regular Meetings

A forum exists for the psychosocial team to meet to discuss clinical, program, professional and administrative issues.

 

STANDARD 18 - Translating Research into Practice

Psychosocial oncology professionals identify research relevant to their practice and incorporate the results of research into practice.

Section IVC - PATIENT AND FAMILY SERVICE IN PSYCHOSOCIAL ONCOLOGY

 

Preamble

Timely and effective psychosocial services, provided to patients and families prevent or reduce distress, enhance coping and quality of life, and improve compliance with therapeutic recommendations.

STANDARD 19 - Information

Information regarding psychosocial and therapeutic resources and services are conveyed in a timely and sensitive manner.

 

STANDARD 20 - Equitable Access of Services

Patients have access to psychosocial services regardless of diversity in diagnosis, cultural/ethnic background, language, gender, sexual orientation, or geographical location. If services are not available in the patient’s community, efforts are made to facilitate access as required.

 

STANDARD 21 - Appropriate Services are Available

Psychosocial programs and services are available and appropriate to the needs of cancer patients and their families.

 

STANDARD 22 - Informed Consent

Patients and their families receive sufficient information about the intended nature of the psychosocial oncology intervention, potential outcomes and other options available to them to make an informed decision before accepting psychosocial care.

 

STANDARD 23 - Advocacy

Psychosocial oncology professionals assist and advocate on behalf of patients and care-givers where real or perceived barriers exist in the provision of optimal care.

STANDARD 24 - Open Referral Policy

Patients and families can self-refer to available psychosocial services. Where direct access/self-referral is not possible (e.g. direct access to psychiatry), it is the responsibility of the psychosocial professional to facilitate the appropriate referral.

 

Section IVD - RESEARCH and PROGRAM EVALUATION STANDARDS FOR PSYCHOSOCIAL ONCOLOGY PROGRAMS

Preamble

Psychosocial oncology research is essential for the advancement of knowledge and the development of services for patients and families. It is of prime importance that the body of knowledge in psychosocial oncology be acquired through research and evaluation and that new knowledge be translated into clinical practice. These standards are elaborated with the intention that University and teaching centres initiate and conduct psychosocial research and that smaller hospitals participate in these studies.

 

STANDARD 25 - Supportive Research Environment

The psychosocial oncology program creates an environment conducive to collaborative research by;

(a) Valuing and encouraging research.

(b) Facilitating collaboration between clinicians and researchers.

(c) Developing linkages with other cancer care facilities, hospitals, universities and research organizations.

(d) Ensuring protected time for clinicians to participate in research activities..

(e) Ensuring that research findings are integrated into clinical practice.



STANDARD 26 -Psychosocial Program Evaluation

The evaluation of psychosocial care and services is integrated into the psychosocial oncology program.

 

STANDARD 27- Research and Ethics Review

Psychosocial oncology research studies have institutional scientific and ethics review.

 

STANDARD 28 - Research Resources Available

The cancer facility ensures or facilitates the availability of financial resources available to support psychosocial oncology research.


Section IVE - PATIENT AND STAFF EDUCATION IN PSYCHOSOCIAL ONCOLOGY

 

Preamble

Education in the field of psychosocial oncology involves planned provision of information to patients, families, psychosocial oncology professionals, other health care providers and the general public. For patients and families the provision of education can facilitate informed decision making and understanding of the cancer experience. The provision of education to psychosocial and other health care providers promotes continuous improvement of programs and professional development.

 

STANDARD 29 - Educational Needs Are Identified

A process is in place for identifying the unique learning needs of patients and their families and caregivers, community groups, governing bodies, and psychosocial oncology professionals.

 

STANDARD 30- Educational Resources are Easily Accessible

Psychosocial educational programs and resources are readily accessible to patients and their families and care-givers, community groups, governing bodies, and psychosocial oncology professionals.

 

STANDARD 31 - Relevance of Educational Material

Educational programs, resources, and materials build on the capacity of the learner and are tailored to the diversity of the intended recipients.

 

STANDARD 32 - Continuing Professional Education

Educational needs of psychosocial professionals are met in accordance with professional competency requirements.

 

STANDARD 33 - Formal Evaluation of Educational Programs

As a component of quality improvement, psychosocial oncology education programs and materials are monitored and evaluated on an ongoing basis.

REFERENCES

Devine, E.C. and Westlake, S. K. (1995) The effects of psychoeducational care provided to adults with cancer: meta-analysis of 116 studies, Oncology Nursing Forum, 22 (9), 1369-1381.

Fawzy, F.I., Fawzy, N.W., Arndt, L.A., and Pasnau, R.O. (1995). Critical review of psychosocial interventions in cancer care. Archives of General Psychiatry, 52 (Feb.1995), 100-113.

Fox, B. H. (1995). The role of psychological factors in cancer incidence and prognosis. Oncology, 9(3), 245-256.

Gotay, C., and Stern, J. D. (1995). Assessment of psychological functioning in cancer patients. Journal of Psychosocial Oncology, 13 (1/2), 123-160.

Hearn, J. and Higginson, I. J., (1997). Outcome measure in palliative care for advanced cancer patients: A review. Journal of Public Health Medicine, 19 (2), 193-199.

Iacovino, V. and Reesor, K. (1997). Literature on interventions to address cancer patients' psychosocial

needs: what does it tell us?. Journal of Psychosocial Oncology, 15 (2), 47-71.

Meyer, T. J. and Mark, M. M. (1995). Effects of psychosocial interventions with adult cancer patients: A

meta-analysis of randomized experiments. Health Psychology, 14 (2), 101-108.

van't-Spijker, A., Trijsburg, R.W., Duivenvoorden, H.J. (1997). Psychological sequelae of cancer diagnosis: A meta-analytical review of 58 studies after 1980. Psychosomatic Medicine, 59 (3), 280-293.

Trijsburg, R. W., van Knippenberg, F.C.E., and Rijpma, S.E. (1992). Effects of psychological treatment on cancer patients: A critical review. Psychosomatic Medicine, Vol. 54, 489-517.

Appendix A

Canadian Association of Psychosocial Oncology (CAPO)

NATIONAL STANDARDS WORK GROUP


(Left to right) Mr. Alan Gavin, London, ON; Dr. Mary Elliott, Toronto, ON; Mr. John Farber, Winnipeg, MB; Dr. Roanne Segal, Ottawa, ON; Dr. Barry Bultz, Calgary, AB; Dr. Michelle Deschamp, Montreal, PQ; Dr. Zeev Rosberger, Montreal, PQ; Mr. Richard Doll, Vancouver, BC. Missing: Ms. Sharon Dublin, Halifax, NS; Missing: Dr. Terry Bunston, Toronto, ON.

 

Members

 

Barry Bultz, Ph.D., Director

Department of Psychosocial Resources

Tom Baker Cancer Centre, Alberta Cancer Board

1331 - 29th Street NW

CALGARY, AB T2N 4N2

Phone: 403-670-1767

Fax: 416-480-2128

Email: bdbultz@acs.ucalgary.ca

Terry Bunston, Ph.D.

Princess Margaret Hospital

Toronto, ON

November 1997 - September 1998

Michele Deschamps, R.N., Ph.D., Chercheure

Direction de la sante publique

Organisation et evaluation des services preventifs

4835, avenue Christophe-Columb

MONTREAL, PQ H2J 3G8

Phone: 514-528-2400 x 3571

Fax: 514-528-2598

Email: mdescham@santepub-mtl.qc.ca

Richard Doll, M.S.W., M.Sc., Provincial Leader

Cancer Rehabilitation Network

BC Cancer Agency

600 West 10th Avenue

VANCOUVER, BC V5Z 4E6

Phone: 604-877-6126

Fax: 604-872-4596

Email: rdoll@bccancer.bc.ca

Sharon Dublin, BSc BN MN RN

Assistant Professor

Department of Nursing

St. Francis Xavier University

P.O. Box 5000

ANTIGONISH, NS B2G 2W5

Phone: 902-867-2434

Fax: 902-867-2322

Email: sdublin@stfx.ca

Joined July, 1998

Mary Elliott, M.D., FRCPC, Co-ordinator of Psychiatry

Department of Psychosocial Oncology

Princess Margaret Hospital

610 University Ave.

TORONTO, ON M5G 2M9

Phone: 416-946-2000 ext 5405

Fax 416-946-2947

Email: Mary_Elliott@pmh.toronto.on.ca

Joined February, 1999

John Farber, M.A., Director

Department of Psychosocial Oncology

Manitoba Cancer Treatment and Research Foundation

100 Olivia Street

WINNIPEG, MB R3E 0V9

Phone: 204-787-1325

Fax: 204-783-6875

Email: john.farber@mctrf.mb.ca

Alan Gavin, M.S.W., C.S.W., Coordinator Psychosocial Research and Education

Supportive Care

London Regional Cancer Centre

790 Commissioners Road E.

LONDON, ON N6A 4L6 Phone: 519-685-8622

Fax: 519-685-8636

Email: agavin@lrcc.on.ca

Zeev Rosberger, Ph.D., Director

Psychology Division

Sir Mortimer B. Davis

Jewish General Hospital

4333 Cote Ste. Catherine Rd.

MONTREAL, PQ H3T 1E4

Phone: 514-340-8210 x 5227 or 4215

Fax: 514-340-8290

Email: zeev@psych.McGill.CA

Roanne Segal, M.D., FRCPC, Medical Director

Oncology Rehabilitation Programs

Ottawa Regional Cancer Centre

501 Smyth Road

OTTAWA, ON K1H 8L6

Phone: 613-737-7700 x 6815

Fax: 613-247-3511

Email: rsegal@cancercare.on.ca

Others Assisting

Stephen Hansen, M.Ed., Provincial Education Leader

B.C. Cancer Agency

600 West 10th Avenue

VANCOUVER, BC V5Z 4E6

Phone: 604-877-6098 x 2505

Fax: 604-877-6144

Email: shansen@bccancer.bc.ca

Carol Smillie, Ph.D., Professor

School of Nursing

Dalhousie University

1st Floor, Forrest Bldg.

5869 University Avenue

HALIFAX, NS B3H 1W2

Phone: 902-494-2032

Fax: 902-494-3487

Email: csmillie@kilcom1.ucis.dal.ca

Joined August, 1998

Marilyn Colton, Assistant Executive Director Cancer Care, Acute Care and Community Care

Canadian Council of Health Services Accreditation

Ottawa, Ontario


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