Caregivers - INTEGRIS Health
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Transcript Caregivers - INTEGRIS Health
Telehospice:
Promising Outcomes and Lessons
Learned from Intervention Studies
Elaine Wittenberg-Lyles, PhD
Associate Professor
Markey Cancer Center/ Department of Communication
University of Kentucky
Telehospice Project Team
Debra Parker Oliver, MSW, PhD
Social Work
University of Missouri
George Demiris, PhD
Bio informatics
University of Washington
Elaine Wittenberg-Lyles, PhD
Communication Studies
University of Kentucky
Karla Washington, MSW, PhD
Social Work
University of Louisville
Funding by
National Cancer Institute, National Institute of Nursing Research, John A. Hartford
Foundation
Background
1.56 million patients who received hospice care
last year in the United States, 83% were age 65 or
greater (National Hospice and Palliative Care
Organization, 2010)
Caregivers perform nursing tasks and deal with
emotional problems while also witnessing their
loved one’s dying process (Pinquart & Sorensen,
2003)
Background
Family Caregivers
Higher risk for deteriorating physical health, depression,
financial challenges and premature death (Dean, 1995;
Sherwood, Given, Given & von Eye, 2005)
Although pain control continues to be among one of the
highest priorities for patients and caregivers during end-oflife care (Downey, Engelberg, Curtis, Lafferty, & Patrick,
2009), medication and pain management are among the
top unmet needs of hospice caregivers (Bee, Barnes, &
Luker, 2009)
Background
Family have identified problems in pain and symptom
management and emotional support from staff
(Hermann & Looney, 2001; Kutner, Kassner, &
Nowels, 2001; Teno et al., 2004)
Very few, if any, evidence-based caregiver
interventions have been translated to or
implemented in practice settings (Northouse et al,
2010)
Telehospice
the use of advanced
communication technologies to
improve the quality of hospice
services delivered to patients
and their families
Telehospice Interventions
Minimize suffering and improve patients’ /caregivers
quality of life at the end of life
What are you currently using?
Adaptation and Utilization
Agency readiness to adopt telehospice
Felt comfortable utilizing technology, but were less comfortable
introducing new technology for use in the patients’ home
Assessment of hospice organizations to accept
technology innovation
Perceived as a useful for documenting meeting processes, staying
informed of care decisions, and developing more collective care plan
goals
Adaptation and Utilization
Telehospice interventions now appear to be more
readily accepted by nursing and administrative staff
members
Assessment of hospice volunteers/coordinators
Have access to computers, Internet, and email at the hospice agency
and report routine use of cellular phones and email
Current Telehospice Projects
Web-based worksheet for expert feedback in
community-based hospice
Hospice Education Network (HEN)
Internet-based platforms such as Care Pages
Support mechanism
Evidence base for Telehospice
26 studies identified from indexed databases (Parker
Oliver et al, in press)
Use
Provider attitudes
Patient/family values
Clinical outcomes (only assessed in 3 studies)
Readiness
Cost
Hospice Philosophy- Relevant
Principles
Hospice Interdisciplinary Team Members: Required to
meet for plan of care every 15 days
Patient and Family are the unit of care- and member
of care plan team
Patient and Family autonomy in decision making
Preliminary work
Do Patients and Family routinely participate in the
interdisciplinary care plan meetings?
Survey of hospices in Missouri- 0%
National survey of social workers
75% never had a family attend
23% seldom
0% routinely had family attend meeting
Problems preventing attendance
Care needs of patient
Distance to office
Confidentiality as people wait in office
Time involved for team members
Intervention: Conceptual Model
Designing an Intervention
Pilot Research
(National Cancer Institute R21)
2 Phase- Mixed Methods Study
Phase 1 Comparison/Control- 6 months
Administer measures for consenting patients
Videotape team meetings for consenting patients
Phase 2 Intervention
Administer measures
Videotape team meetings
Two hospice programs- total of 5 teams
Outcomes
Feasibility: Videotape meetings and observe
Impact: Interviews
Outcomes:
Caregiver Pain Medicine Questionnaire
Caregiver and Patient Quality of Life
R21 Results
Total N= 75 caregivers (Phase 1= 41 Phase
2=34).
75 caregivers took care of 68 patients
R21 Results
Caregiver perceptions of pain medications
The subscale reluctance to report was significantly associated
with phase (P < .01) and with baseline score (P < .03).
More likely to report pain and more tolerant of pain
medications
No significant difference in administration of pain medication
Quality of life
No significant differences in caregivers or patients
Current Project
The ACTIVE Intervention to Improve Hospice
Caregiver Pain Management
Multi-site RCT
500 caregivers
4 years
Web based video-conferencing
R01NR011472 , D. Parker Oliver PI, Wittenberg-Lyles, Co-I
ACTIVE: Assessing Caregivers for Team
Intervention via Video Encounters
Using secure Internet
connection caregivers and
patients can join the hospice
IDT and participate as a
member of the team
Requires yearly subscription
to website, high speed
Internet and webcam
Specific Aims
1.
Test effectiveness – caregiver’s ability to manage pain
2. Evaluate cost-effectiveness
3. Evaluate potential for translation
In 2009 there were only 114 active NIH
grants in palliative care, less than 1% of
the total funded research from NIH
Example – The Van
R 21 Results- Communication
Meetings are led primarily by nurses
Interpersonal communication and information flow are not
always efficient
Sometimes a struggle for control rather than collaboration
Collaboration-- Requests for clarification and the offering
of information
Caregivers are active participants and ask numerous
questions, especially related to pain control
Although pain issues make up more than a third of the
team discussions, if caregivers are not present, their
perceptions and concerns about pain management issues
are not discussed
Comparison
Example- “Here’s my problem”
Caregiver Talk
Example – “He’s 92…”
Caregiver Interviews
It’s almost like they bring the hug. You’re
isolated in your own home and family
members don’t even come by. And it’s like
you have that hand on your shoulder with the
phones and the faces…and it made a big
difference.
Example - Providing support
Example – “I feel like I’m lying”
Caregiver Interviews
“The nurses that were coming out here were
fine…but it was just nice to get other
people’s input, too.”
Another caregiver stated that she was
impressed to learn that “a whole team of
people” worked together to provide care for
her husband.
And for hospice staff
… my mind was narrowed to a point where I
thought that the “team” was the team that
was here [in the agency office], not realizing
and accepting that the team also included
the family and patients. Even though I
could say it…I didn’t feel it.
Staff Interviews
A medical director noted, “…it helps me take
better care of the patient. I know what to
do better when I can talk to them and see
them.”
“It’s really nice to observe how other
members of our team interact with
[caregivers]. I think we can learn from each
other.”
Translational Lessons
Recruitment
Special initiatives
Changing technology
Different organizational
environments/cultures
Findings
The intervention is not only feasible, but that it holds
promise to change caregiver perceptions of pain
management and potentially reduce patient pain.
Caregivers can and do talk freely to the hospice team
about pain concerns and Hospice staff members are
positive about the intervention.
The preliminary observation of these encounters is giving
insight on ways hospice team members can improve
collaboration and overall patient care, including patient
safety concerns.
Telehospice
Problem-Solving Therapy for
Hospice Caregivers
Problem Solving Therapy
PST is defined as “the self-directed cognitivebehavioral process by which a person attempts to
identify or discover effective or adaptive solutions for
specific problems encountered in everyday living.
(D’Zurilla & Nezu, 2007)”
ADAPT
A=Attitude
D=Define the problem
A=Alternatives (generate alternatives for overcoming
the identified obstacles and achieving goals)
P=Predict (predict positive and negative
consequences and select one)
T=Try Out (implement the solution in real life and
monitor its effects) (D’Zurilla & Nezu, 2007)
PST and Telehospice
Compare face-to-face with videophone delivery
Outcome measures included caregiver anxiety,
quality of life and problem solving abilities, as well as
technical quality of video-sessions and satisfaction of
the intervention
Results
126 caregivers were recruited in the study
77 face-to-face and 49 on videophone
PST delivered via video was not inferior to face to
face delivery.
Caregiver quality of life improved and state anxiety
decreased under both conditions.
Audiovisual feedback captured by technology may be
sufficient
Caregiver interviews
One participant stated that the videophone provided
“a face behind the voice. I really enjoyed it… You were
here… It was a personal touch. Although you did make
me fix my hair so early in the morning.”
Caregiver interviews
“At first I thought it would not make a difference… I
really liked it more than I thought I would. This made it
homey, much more personal. You are here with me and
I am talking to you.”
Caregiver interviews
One of them commented on the slight time delay
between audio and video (“it was distracting at times
in the beginning, because of the time lapse”) and the
other did not see an added element compared to a
regular phone (“it was nice, but I think I can do this just
as well without the picture”). One participant who
experienced problems in establishing a connection
stated “when it works it is great, but I have old lines
here in the house, and sometimes it didn’t work.”
Additional Research Questions
Who benefits most from the intervention and how
can we identify them upon admission?
How can staff express empathy over virtual media?
Do long distance caregivers and residents in the
nursing home have additional benefits?
What is the cost of the intervention to hospices?
How does the intervention need to be modified to
translate into everyday practice for hospice
providers?
Things to think about…..
Would incentive payments increase the use of
telehospice?
What are the ethical issues you see in the use of
telehospice?
Is it feasible for your hospice to implement the
ACTIVE intervention- why or why not?
Thank you!
www.telehospice-project.org
Facebook: The Telehospice Project
Email: [email protected]