The FOCUS Program: Helping Cancer Patients and Family Their Caregivers. Laurel Northouse PhD, RN, FAAN Professor of Nursing University of Michigan

Similar documents
Family Caregiving Issues that Cancer Survivors and their Caregivers Face

COPE Intervention for Cancer Caregivers

ONCOLOGY NURSING SOCIETY RESEARCH AGENDA. Prepared and Submitted by. Ann M. Berger, PhD, APRN, AOCN, FAAN ONS Research Agenda Team Leader

Stanford Self-Management Programs Effectiveness and Translation

Qualitative Analysis of Health Literacy Needs of Rural Cancer Patients From Six UW Out Reach Clinic

Patient Navigation & Psychosocial Care. Angelina Esparza, RN, MPH Director, ACS Patient Navigator Program & Cancer Resource Centers

Patients with Cancer and Family Caregivers: Management of symptoms caused by Cancer or Cancer Therapy at Home

Breast Survivorship Clinic Follow-up Patient Satisfaction Survey Abstract

Usability Testing of an Online Self-Management Program for Adolescents with Cancer

Identifying Research Questions

Ian Nisonson, M.D. 11/2/2017

Implementation Model. Levels of Evidence 3/9/2011. Strategies to get Evidence into Practice EXTRACTING. Elizabeth Bridges PhD RN CCNS, FCCM, FAAN

Sustaining the practice

Interventions to help the family cope

What will the PCMH Look Like in 2014? Joseph E. Scherger, MD, MPH

QUALITY OF LIFE OF CANCER CHILDREN CAREGIVERS

Social and Behavioral Sciences (SBS)

DRAFT Optimal Care Pathway

Background. Population/Intervention(s)/Comparison/Outcome(s) (PICO) Interventions for carers of people with dementia

MEETING THE CHALLENGE OF BURNOUT. Christina Maslach, Ph.D. University of California, Berkeley

Course Materials & Disclosure

Communication with Surrogate Decision Makers. Shannon S. Carson, MD Associate Professor University of North Carolina

Connecticut TF-CBT Coordinating Center

Evidenced-Informed Training Intervention For Puerto Rican Caregivers of Persons with ADRDP

Summer Huntley-Dale, PhD, RN Assistant Professor Western Carolina University

The Future of Nursing in Eliminating Health Disparities

Measuring self-efficacy for caregiving of caregivers of patients with palliative care need: Validation of the Caregiver Inventory

Advance Care Planning: Goals of Care - Calgary Zone

ASSOCIATION OF CHILD LIFE PROFESSIONALS MESSAGE HANDBOOK

Liberating Restricted Visiting Policy in Greek Intensive Care Units: Is it that complicated?

Stress-Busting Program. An Evidence-Based Program for Family Caregivers

BMT CAREGIVER CHALLENGES. Presented by: Meagan Dwyer, Ph.D., Elizabeth Muenks, Ph.D. and Liliana Delano

Administrative Approval: Vice President of Professional Services

Text-based Document. Staff Response to Flexible Visitation in the Post- Anesthesia Care Unit (PACU) Voncina, Gail; Newcomb, Patricia

AWARD NUMBER: W81XWH TITLE: Care Planning for Prostate Cancer Patients on Active Surveillance. PRINCIPAL INVESTIGATOR: Dr.

Group-Based Interventions for Caregivers of Individuals with Chronic Health Conditions. Kelly Valdivia, BA and Stacy A.

INNOVATIVE TOOLS TO SUPPORT FAMILY CAREGIVERS

The Resilience in Illness Model: Dialogue on Applicability in Other Illness Conditions and Difficult/Traumatic Life Circumstances

MAYERSON CENTER FOR SAFE AND HEALTHY CHILDREN TRAINING OPPORTUNITIES

CRITICALLY APPRAISED PAPER (CAP) FOCUSED QUESTION

CMS Oncology Care Model s Standards for Patient Navigation

Patient and Provider Perspectives of Self-Management of Ulcers in SCI/D

Models for Patient-centered Cancer Care

Caregivers: Quarterback, Cheerleaders and Caring for Self

Statewide Implementation of Reducing Disability in Alzheimer s Disease: Challenges to Sustainability

Colorectal Recovery Package & Risk Stratified Pathways. Julie Burton Lead Colorectal / Stoma Care CNS Nurse Endoscopist

Physicians Who Care for People with MS

Critical Review: What effect do group intervention programs have on the quality of life of caregivers of survivors of stroke?

A Model of Health for Family Caregivers. Flo Weierbach, RN, MPH, PhD East Tennessee State University College of Nursing

Perceptions of Family Cancer Caregivers in Tanzania: A Qualitative Study. Allison Walker

Burnout in Palliative Care. Palliative Regional Rounds January 16, 2015 Craig Goldie

10 Steps to Maximizing Nurses Full Scope of Practice Utilization in Primary Care Settings

HKCE Symposium on Community Engagement VIII

Promoting Colorectal Cancer Screening in Rural Emergency Departments

Admissions, Readmissions & Transitions Core Functions & Recommended Actions

03/24/2017. Measuring What Matters to Improve the Patient Experience. Building Compassion Into Everyday Practice

Implementation and Dissemination Science in Cancer Survivorship Care Delivery

Supporting Caregivers across the Care Continuum

THE HEALTH PSYCHOLOGIST S ROLE. Alexandra Nobel, MA Fall 2015

Caregiving: Health Effects, Treatments, and Future Directions

Resilient Living AMIT SOOD, M.D. PROFESSOR OF MEDICINE MAYO CLINIC

Caring for Carers. Includes Caregiver Health Checklists

Quality Of Life, Spirituality and Social Support among Caregivers of Cancer Patients

2014 ONS Distinguished Researcher Award Susan C. McMillan

Using the patient s voice to measure quality of care

Improving Transition Home through a Standardized Discharge Process. Christopher D. Baker, MD Associate Professor of Pediatrics May 10, 2016

Text-based Document. The Relationship Among Change Fatigue, Resilience, and Job Satisfaction of Hospital Staff Nurses. Authors Brown, Robin J.

Shared Decision Making When there is more than one right option

PACT AS A READMISSION REDUCTION STRATEGY KAISER PERMANENTE - COLORADO REGION

A nursing intervention to assist in the management of breathlessness Meeting with Community Partners, Bayshore Friday November 9 th, 2007 Cathy

Community Support Team

Presentation Goals. Presentation Outline. Grant Overview. Stanford University's Model Benefits Overview of MyCD and Tomando Programs

Turkish Nurses Attitudes towards Patients with Cancer

Wellness along the Cancer Journey: Caregiving Revised October 2015

NANDA-APPROVED NURSING DIAGNOSES Grand Total: 244 Diagnoses August 2017

Health Care Ethics and Safety: A Quality Case for Consumer Engagement April 24, Panelist. Susan Hassmiller, RN, PhD, FAAN

Pain Management Education for Nurses: Simulation vs. Traditional Lecture A Comparative Parallel-group Design Study

TBI and the Caregiver. TBI and the Caregiver. The Role of the Caregiver after Traumatic Brain Injury TBI TBI DR. CHIARAVALLOTI HAS NO

Employee Benefit Research Institute. Key Learnings for Employers from the Gallup Healthways Well-Being Index

Research Questions. Respite and Developmental Disabilities. Respite Care Some background. Flexible Funds: What we know

Online Interventions for Dementia Family Caregivers: What We Know/What Next?

The Future of Nursing Research in Jordan

Objectives. Brief Review: EBP vs Research. APHON/Mattie Miracle Cancer Foundation EBP Grant Program Webinar 3/5/2018

Evidence-Based Programs for Caregivers: Vision and Strategy of RCI and the National Quality Caregiving Network

In Search of Patient Engagement. Presentation to National Medical Home Summit February 28 th 2012

Lessons From Infection Prevention Research in Emergency Medicine: Methods and Outcomes

Symptoms and stress in family caregivers of ICU patients. Hanne Birgit Alfheim RN, CCN, PhD student Photo:

Role Play as a Method of Improving Communication Skills of Professionals Working with Clients in Institutionalized Care a Literature Review

Understanding the Relationship Between Nurse Engagement and Patient Experience. Session ID: 467

A Journey from Evidence to Impact

Durham Connects Impact Evaluation Executive Summary Pew Center on the States. Kenneth Dodge, Principal Investigator. Ben Goodman, Research Scientist

Head and Neck Survivorship Clinic Follow-up Patient Satisfaction Survey Abstract

Implementation in Health Care and Social Service Systems: REACH VA

The Promise of Care Coordination: Models That Decrease Hospitalizations and Improve Outcomes for Beneficiaries with Chronic Illnesses

Shedding Light on Bullying in Nursing

Mark Linzer MD General Internal Medicine Office of Professional Worklife Hennepin County Medical Center

Oncology Patient Navigation: Past, Present and Future

The START project: Getting research into the patient pathway

Effective Communication Between Elders and Providers

Returning to the Why: Patient and Caregiver Suffering and Care. Christy Dempsey, MSN MBA CNOR CENP SVP, Chief Nursing Officer

Transcription:

The FOCUS Program: Helping Cancer Patients and Family Their Caregivers Laurel Northouse PhD, RN, FAAN Professor of Nursing University of Michigan Co-director, Socio-behavioral Program U of M Comprehensive Cancer Center

Overview Significance of the Research Description of the FOCUS Program Results from Three Randomized Trials Dissemination Plans

Significance of Research The effects of cancer extend from patients to family caregivers Like a stone dropping in a pond

Reciprocal Relationship in Partners Emotional Distress Patient r =.29 Spouse Couples react as an emotional system

Patients Symptoms Affect Spouses As patients symptoms increase, spouses report a decrease in quality of life Patient symptoms Urinary incontinence Erectile dysfunction Fatigue Spouse Effect Social quality of life Sexual satisfaction Quality of life

Emotional Toll on Spouse Caregivers Spouses report more symptoms of depression than patients in advanced phase of illness Clinical Depression p value Patients 23% <.0001 Spouses 39% Braun et al. JCO 2007

Why Help Family Caregivers of Cancer Patients? Affected by illness -- co-suffers Lack preparation for caregiving role Little support from health professionals Distressed caregiver hinders patient s adjustment

Description of the FOCUS Program q Delivered by a Masters-prepared nurse

Core Program Content F = Family Involvement O = Optimistic Attitude C = Coping Effectiveness U = Uncertainty Reduction S = Symptom Management

F = Family Involvement Promote open communication Encourage mutual support and teamwork Identify family strengths Help children in the family to cope

Promote Family Communication

O = Optimistic Attitude Encourage optimistic thinking Sharing fears and negative thoughts Maintaining hope

Optimism Brochure

C = Coping Effectiveness Help them cope with stress Encourage healthy lifestyle behaviors Identify possible benefits of illness

Help Families Cope

U = Uncertainty Reduction Provide information about treatments and medication Teach them how to obtain information from professionals or other trusted sources Help them live with uncertainty

S = Symptom Management Assess symptoms in patient and family caregiver Teach them self-care strategies

Teach Symptom Management

Treatment Fidelity Nurses followed a 21-page protocol checklist of interventions Nurses audio-taped randomly selected sessions Nurses gave case presentations at monthly intervention meetings

Intervention Team Masters-prepared Nurses Completed 42-hour training program Viewed FOCUS training video New nurses accompanied experienced nurses on home visits to learn role Nurses maintained own caseload of couples

Evaluation of FOCUS Program Breast Cancer Clinical Trial American Cancer Society Prostate Cancer Clinical Trial National Cancer Institute Advanced Cancer Clinical Trial National Cancer Institute

The FOCUS Study Initial Trial Recurrent Breast Cancer Patients and Family Caregivers Sample: 134 patients and their caregivers Funded by American Cancer Society

Purpose of Study To test the effects of a family intervention (FOCUS Program) on patient and spouse outcomes Appraisal variables Coping resources Quality of life

STRESS-COPING FRAMEWORK Antecedents Mediators Outcomes Factors Person Social Disease treatment F O C U S Appraisal Threat Hopelessness Uncertainty Coping Resources Coping Strategies Quality of Life Patient Caregiver

Study Design Randomized Clinical Trial Eligible Couples Random Assignment Control Group Standard Care Experimental Group Standard Care + FOCUS Program

Program Delivery Initial Phase Booster Phase Home Visit 1 Home Visit 2 Home Visit 3 Phone Call 1 Phone Call 2

Study Results Intervention vs Controls Patients Less negative appraisal of illness F = 4.49, p =.04 Less hopelessness F = 9.48, p =.002 Caregivers Less negative view of caregiving F = 3.90, p =.04 Northouse et al., Psycho-Oncology, 2005

FOCUS Study Second Trial Adapted to Prostate Cancer N = 222 dyads Includes 3 phases of prostate cancer Funded by the National Cancer Institute

STRESS-COPING FRAMEWORK Antecedents Mediators Outcomes Factors Person Social Disease treatment F O C U S Appraisal Threat Hopelessness Uncertainty Coping Resources Coping strategy Self-efficacy Communication Quality of Life Patient Caregiver

Study Design Randomized Clinical Trial Eligible Couples Stratified by: Research Site Phase of Illness Treatment Control Group Random Assignment Experimental Group Standard Care Standard Care + FOCUS Program

Revised Program Delivery FOCUS Program 5 contacts Home visit Phone Call Home visit Phone Call Home visit Delivered over three-month period

Longitudinal Assessments Baseline 4 mo. 8 mo. 12 mo. Time 1 Time 2 Time 3 Time 4 Intervention or Control

Prostate Study Results: Patients Intervention vs Controls Less uncertainty F = 3.69, p =.03 Better communication F = 3.48, p =.03 Higher quality of life F = 3.21, p =.07 No differences: appraisal of illness, hopelessness, symptoms, or self-efficacy Northouse et al. Cancer, 2007

Prostate Study Results: Spouses Intervention vs Controls Less negative appraisal F = 8.54, p =.002 Less hopelessness F = 4.15, p =.03 Less uncertainty F = 7.43, p =.009 More self-efficacy F = 3.83, p =.02 Better communication F = 9.71, p =.002 Higher quality of life F = 8.91, p =.004

Satisfaction with Intervention Satisfaction Scores 1 5 low high Patients mean satisfaction score = 4.5 Spouses mean satisfaction score = 4.5

What did we learn? Both patients and caregivers benefit from an intervention Some participants need the intervention more than others Rethink the one-size-fits-all interventions Examine risk-for-distress and intervention dose

Current Study Risk for Distress and Intervention Dose Aim 1. Compare two doses of family intervention vs. control Aim 2. Examine effect of patient risk for distress on study outcomes

Current Study Design

Screening for Risk for Distress Assesses risk of future emotional distress A multi-dimensional scale Predicted high and low distress in 73% of patients screened at baseline

Determining Risk Status Range of Risk for Distress Scores 0 24 low high 8 and below 9 and above Preliminary results from current study: Range of RFD scores: 1 to 19

Sample Advanced cancer patients and caregivers Target: 475 patient-caregiver dyads Currently enrolled: 440 dyads Enrollment rate: Overall 68% Retention rate: 69%

Data Collection and Intervention

Study Still in Progress Enrollment should be completed May, 2009 Results of Randomized Clinical Trial available in Fall, 2009.

Translation Efforts to Date Prostate FOCUS program will be available on NCI Cancer Planet web-site (coming soon) Intervention protocol Staff training manual All brochures and handouts Plans to translate program to tailored webbased program

Future Dissemination Plans: FOCUS Program Research funding to facilitate translation to clinical and community settings Analysis of cost savings and cost of delivery Consider application to other chronic illnesses

Summary Testing family-based interventions Identifying families at risk of distress Examining intervention dose Translating intervention to practice