HTF 402 National First Nations Telehealth Research Project
Project Evaluation
1. Evaluation Questions
The evaluation addressed three issues central to the project objectives:
- telehealth impacts on patient and community access to needed,
quality care
- role of telehealth in health services delivery, including cost-effectiveness
and
- linkages of telehealth with existing health resources.
Since each community among the five is unique, the evaluation
attempted to gather information relevant to each as well as to
telehealth in First Nations' communities in general.
Evaluation questions relating to each of the above issues were
developed though the literature review, the needs assessments and
consultations with project officers, with support from existing
general frameworks for evaluation questions, including Treasury
Board guidelines2 and other major approaches to evaluation
of health and social programs3. The main evaluation
questions are shown in Table 2 below, while site specific questions
are addressed in later chapters about each community.
2 Treasury Board of Canada, Program Evaluation Branch,
Office of the Comptroller General (1991). Program Evaluation Methods:
Measurement and Attribution of Program Results. Ottawa: Minister
of Supply and Serices; Treasury Board of Canada, Program Evaluation
Branch, Office of the Comptroller General (1989). Working standards
for the evaluation of programs in federal departments and agencies.
Ottawa: Minister of Supply and Services.
3 Stufflebeam, D. (1987). The CIPP model for program
evaluation. in G. Madaus, M. Scriven, D. Stufflebeam (Eds.), Evaluation
Models: Viewpoints on Educational and Human Services Evaluation.
Boston: Kluwer-Nijhoff.
Table 2: Evaluation questions
- Issue: Access to needed, quality care
Specific Evaluation Questions: To what extent do the
telehealth applications respond to the community's needs, as
defined by the needs assessment? To what extent do patients and
families find each telehealth application acceptable? To what
extent has telehealth improved access to needed, quality care?
To what extent are services provided through telehealth consistent
with established means of improving patient health outcomes?
- Issue: Health services delivery
Specific Evaluation Questions: To what extent has telehealth
use been organized successfully? To what extent have the professional
skills and competencies required for telehealth been identified
and successfully addressed through training? To what extent are
telehealth applications used by eligible patients in the community?
To what extent does telehealth improve competencies and confidence
of local health personnel?
- Issue: Health services delivery (continued)
Specific Evaluation Questions: How does telehealth affect
staff workload, task allocation and professional practices? To
what extent does telehealth result in cost increases, decreases
or shifts for health service delivery within the communities?
What is the level of technical success of the platforms, applications
and suppliers in the implementing communities?
- Issue: Linkages among health resources
Specific Evaluation Questions: To what extent is telehealth
appropriated, integrated and sustained as a part of the community's
self-governed health care system? To what extent have the telehealth
applications become linked and integrated to provincial initiatives?
To what extent does telehealth improve access of secondary, tertiary
and education providers to local health service providers? To
what extent does telehealth improve health service providers'
awareness and knowledge of local conditions and resources?
2. Evaluation Methods
The overall approach to the evaluation used multiple methods to
assess changes over time from the perspectives of patients, personnel,
communities and other stakeholders. Consistent with the overall
project philosophy, communities were involved in developing the
evaluation methodologies. After developing an initial evaluation
plan (Appendix 8), the evaluation team visited each of the communities
at the beginning of the implementation period (spring 2000) in
order to develop and adapt the proposed evaluation instruments
and procedures to each community needs and functioning. As a result,
the data collection methods and instruments varied somewhat from
community to community.
Monitoring telehealth system usage
Monitoring the usage of the telehealth applications provided information
on the nature, level, quality and implications of usage. The main
data collection tools were patient encounter forms completed by
nursing station personnel and by remote health providers (Appendices
2 and 3).
Nursing station patient encounters. During the
study period, nursing station staff recorded basic information
about each encounter with patients using the telehealth applications,
on a checklist-type form immediately after each telehealth usage.
The forms included:
- date, time and length of usage, as a proportion of total encounter
- the type of health problem prompting the consultation
- who was present, at the local and remote sites
- what was done during the telehealth encounter
- the results of the visits in terms of subsequent actions
- any technical problems during the usage
- the implications of using telehealth in terms of costs incurred
or avoided.
The section of the forms recording what was done during the visit
provided indicators of quality of care. For the telehealth applications
that addressed conditions for which guidelines for appropriate
primary clinical practice have been established (diabetes, mental
health, and cardiology), the forms included checkpoints for the
recommended components of appropriate care.
The forms were also used to record usage of telehealth for patient
education, continuing professional education, and community development.
In Fort Chipewyan, a different system was used, based on a utilization
record developed by the vendor and modified to accommodate the
evaluation.
Each patient was assigned an identifier code, used on all visits
to the nursing station during the study period. The telehealth
coordinators in each community were responsible for assigning codes
to patients and for maintaining a master list of patients' names
and codes. No nominative information was sent outside the nursing
station.
The telehealth coordinator in each site faxed the completed encounter
forms every two weeks to the evaluation team. These were received
at a secure fax site at McGill University.
Over the evaluation period, information was received about 927
telehealth sessions involving 176 patients. The number of sessions
per community varied from 40 to 755, and the number of patients
seen from 17 to 59.
Remote centre patient encounters. Practitioners
(nurses or physicians) in the remote centres completed brief patient
encounter form after each telehealth encounter for patients in
the study group in each site. This encounter form included:
- date, time and length of usage
- what was done during the telehealth encounter
- the results of the visits in terms of subsequent actions
- any technical problems during the usage
- the implications of using telehealth in terms of costs incurred
or avoided.
These forms were also regularly faxed to the evaluation team,
using the same patient identifier as in the community form. Remote
encounter forms were not completed for the Southend project.
Patient satisfaction
Patients using telehealth in each community were asked to complete
a brief satisfaction questionnaire about their reactions to and
comfort with the telehealth system. This questionnaire was based
on an instrument developed by Saskatchewan's Northern Telehealth
Network (see Appendix 4 for the different versions of this questionnaire
used in each community). A total of 110 questionnaires were received.
Qualitative interviews
Qualitative interviews were conducted at the end of the project
during in depth data-gathering visits to each community (in February
and March 2001). They were conducted with stakeholders in each
community and in the participating health systems, using semi-structured
interview guides. The stakeholders were asked to respond as key
informants giving their views on the evaluation questions from
their perspectives within the project and the communities. They
were identified in collaboration with project leaders and nursing
station staff. The interview guides may be found in Appendix 5.
The interviews lasted from one half hour to three hours in length.
Some were conducted as group consultations, and some were conducted
by telephone or videoconference. If participants gave permission,
they were tape-recorded.
The table below summarizes the qualitative interviews conducted
about each community:
Table 3: Summary of interviews conducted about each community
- Community: La Romaine
Number of Interviews: 9 interviews with 9 individuals
Types of respondents: Telehealth coordinator,
nursing staff, director, remote providers, remote telehealth
coordinator, provincial telehealth representatives, vendor
- Community: Berens River
Number of Interviews: 9 interviews with 14 individuals
Types of respondents: Telehealth coordinator/project
officer, telehealth supervisor, nursing staff, community workers,
remote providers and educators, remote telehealth coordinator
- Community: Southend
Number of Interviews: 13 interviews with 20
individuals
Types of respondents: Telehealth coordinator,
nursing station board members and management, nursing and mental
health staff, community workers visiting and remote providers,
remote telehealth coordinator, provincial telehealth representative,
project officers
- Community: Fort Chipewyan
Number of Interviews: 12 interviews with 22
individuals
Types of respondents: Telehealth coordinator,
Band and nursing station managers, nursing staff, nursing station
board member, elders, patients, tertiary providers and management
, provincial telehealth representatives, Health Canada representative
3. Ethical Issues
The conduct of the evaluation respected the principles and assumptions
of the Project Accountability framework, as well as the Ethical
Principles for Research with First Nations Communities set forth
in Chapter 6 of the Tri-Council Policy Statement on Ethical Conduct
for Research Involving Humans. To protect community privacy, the
procedures were designed so that the evaluation team had no access
to any patient identification information.
In its initial visits to the communities, the evaluation team
discussed ethical issues with community representatives, and where
deemed appropriate, obtained formal authorization from the Band
for the study according to the agreed-upon ethical principles.
In those communities that required it, each patient using telehealth
completed a consent form for participation in the project and/or
the evaluation, at the time of their first visit. The telehealth
system was explained, stating that the care provided would be equivalent
to usual care. The evaluation procedures and the procedures for
ensuring confidentiality were explained, as was the voluntary nature
of participation without prejudice to care or services. The signed
consent forms were retained in nursing station files.
Key informants were not asked to sign a consent form, as participation
in this type of assessment was considered as part of their normal
roles or professional responsibilities. However, they were formally
asked for consent to participate and told that their responses
would be kept confidential, and that no respondent would be identified
in the evaluation reports.
A complete operational research protocol was prepared for the
entire project, for submission to Research Ethics Review Committee
in research and medical institutions, which required it. This may
be found in Attachment 6.
4. Analyses
All data from the patient encounter forms and satisfaction questionnaires
were entered into databases and analysed using SPSS. Qualitative
data from the key informant interviews was transcribed and analysed
using matrix analysis techniques. For the economic analysis, the
cost-consequence analysis matrix developed by McIntosh & Cairns
was used (1999).
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