Systemic Sclerosis Clinical Trial
Official title:
The Scleroderma Patient-centered Intervention Network (SPIN) - Scleroderma Support Group Leader EDucation (SSLED) Program Feasibility Trial
Many people living with a rare disease turn to peer-led support groups to cope with their
condition and access educational resources. Systemic sclerosis (SSc), or scleroderma, is a
rare autoimmune connective tissue disease where peer-led support groups play an important
role. There are currently approximately 200 SSc support groups in Canada and the US, most of
which are led by people with SSc. Many SSc patients, however, cannot access support groups.
In other cases, support groups are not sustained due to factors that include the burden on
group leaders living with a serious, unpredictable disease and limited group leadership
skills of some untrained leaders. Our partners from Scleroderma Canada and the Scleroderma
Foundation in the US are committed to improving support group accessibility and
effectiveness. These organizations maintain a list of active support groups, but currently do
not provide training or other resources to groups or their leaders. To address this gap, our
team, including investigators and patients from the Scleroderma Patient-centered Intervention
Network (SPIN), developed the Scleroderma Support group Leader EDucation (SPIN-SSLED)
Program, which is designed to improve support group leader confidence and self-efficacy,
reduce burnout, improve emotional well-being, and improve health-related quality of life.
In the planned full-scale randomized controlled trial (RCT) that will follow our feasibility
trial, we will evaluate whether the SPIN-SSLED Program is effective in improving SSc support
group leaders' self-efficacy for carrying out their leader role (primary) and if it reduces
burnout, improves emotional well-being, and improves health-related quality of life
(secondary). Thus, the SPIN-SSLED Feasibility Trial answers the following research questions:
(1) Is a full-scale SPIN-SSLED RCT feasible? (2) Are adaptations needed to the research
design for the planned full-scale RCT? (3) Are there ways to improve the SPIN-SSLED Program
for delivery in the planned full-scale RCT based on input of support group leaders who
participate in the feasibility trial?
People with rare diseases experience many of the same challenges as those with more common
diseases, but also face unique challenges, including gaps in knowledge about their disease
and limited treatment and support options. Professionally organized support services are
often available for people with more common diseases but are not typically available for
people with rare diseases. Instead, many people with rare diseases rely on peer-led support
groups for education and to cope with their disease. Support groups may be held face-to-face
or online, led by professionals or peers, and have a structured or an unstructured format.
Activities typically involve an educational or information-sharing component and the exchange
of emotional and practical support.
SSc is a rare, chronic, autoimmune connective tissue disease characterized by abnormal
fibrotic processes and excessive collagen production. Peer-led support groups play an
important role for people with the disease. There are currently approximately 200 active SSc
support groups listed by Scleroderma Canada or the Scleroderma Foundation in the USA, most
led by people with the disease. Many people with SSc, however, do not have access to SSc
support groups, and many support groups that are initiated are not sustained due to obstacles
that could be addressed by providing training to support group leaders. Challenges for
patient support group leaders, particularly in rare diseases, include practical difficulties,
such as a lack of resources or poor coordination with medical professionals and leader
organizations; difficulties with group leadership tasks, such as managing complex group
dynamics; and personal challenges, such as managing one's own health condition while
supporting others and preventing burnout.
A training and education program could provide the necessary information and skills to
improve the ability of SSc peer support group leaders to lead sustainable, effective support
groups; reduce their emotional and physical burden; and encourage new leaders to set up
support groups where none exist or via the internet. In rare diseases, face-to-face delivery
of such a training program is not feasible because current and potential leaders are widely
dispersed geographically. Videoconferencing has been used successfully to train educators,
health service providers, and parents of children with behavioural difficulties, for example,
and is as effective as face-to-face training.
The SPIN-SSLED Program was developed by a team of researchers with expertise in SSc, patient
organization representatives, and a Patient Advisory Board comprised of current SSc support
group leaders. The program content and design are based on results of our preliminary
research on support groups in SSc and informed by instructional material for support group
leaders we identified via the internet and by consultations with support group leaders. The
program uses a problem-based learning approach. Problem-based learning is a learner-centered
approach that integrates theory and practice by providing the necessary knowledge and skills,
presenting a complex, real-world problem, then working to identify an approach to solving the
problem. To implement this, each module, or learning session, will introduce a topic and
provide an overview of key information. Then, there will be a guided discussion among
training group participants about possible approaches and solutions. The program includes 13
modules that will be delivered live via webinar over the course of the 3-month program. In
addition to the live modules, SPIN-SSLED participants will receive a workbook that summarizes
didactic material that is provided and will be shown filmed vignettes demonstrating effective
group facilitation techniques and ways to respond to support group issues. SPIN-SSLED
participants will also have access to an online resource center that includes a range of
helpful tools for leaders including files of SSc related videos to show at meetings and an
online forum for leaders to post questions, open only to leaders enrolled in the training
program.
The proposed SPIN-SSLED Program Feasibility Trial builds on this background research and will
evaluate the feasibility of delivering the SPIN-SSLED Program and of our planned full-scale
trial design. The objectives of this study are (1) To evaluate the feasibility of steps
needed to take place in the full-scale trial, including the required resources (e.g.,
staffing, time, and budget), management issues (e.g., related to optimizing performance of
personnel and data systems), and scientific aspects (e.g., recruitment of eligible leaders,
fidelity of intervention delivery, acceptability of intervention to leaders, assessing
performance of outcome measures); (2) To make any necessary modifications to the SPIN-SSLED
Program based on participant feedback
The aim of the SPIN-SSLED Feasibility Trial is to collect data related to the study's
process, in order to assess the feasibility of the steps that need to take place as part of
the main study; required resources (e.g., staffing, time, and budget), management issues
(e.g., optimizing performance of personnel and data systems); and scientific aspects (e.g.,
recruitment rates of eligible leaders, fidelity of intervention delivery, acceptability of
intervention to leaders, performance of outcome measures).
Our partners from the Scleroderma Canada and the Scleroderma Foundation will contact group
leaders to describe the SPIN-SSLED Feasibility Trial and ascertain interest in participating.
SPIN-SSLED personnel will send email invitations with the consent form to interested support
group leaders. Following this, support group leaders will be contacted by phone within 48
hours to describe the study, review the consent form, and answer questions assessing
eligibility. Eligible patients who verbally accept the offer to enrol in the study will
receive an email with the consent form for the study, which they can sign by replying, "I
have read the consent form and understand the terms of the feasibility study. I agree to
participate in the study testing the feasibility of the SPIN-SSLED Program." We will enroll
10 SSc support group leaders to participate in the program. Based on our previous experience
with videoconferencing and consistent with previous trials of videoconference training, to
maximize effective interaction and participation, 5 group leaders will be assigned to each
training group. Training sessions will be delivered using the GoToMeeting® videoconferencing
platform, a high-performance platform that has been used successfully for similar
applications.
A survey will be administered to all participants before the trial. The survey will contain a
demographics questionnaire designed for this study that includes basic demographic
information, such as gender, age and employment status. The survey also includes
disease-related variables, such as years since scleroderma diagnosis and questionnaires for
all outcome measures. These questionnaires will be administered again upon completion of the
program, along with a satisfaction questionnaire. All questionnaires will be completed using
the online surveying tool Qualtrics. Once the online survey data is collected, data will be
exported to the statistics software program, IBM SPSS.
A description of feasibility outcomes will be presented, including leader eligibility and
recruitment, leader enrolment and randomization, technological performance of the
videoconferencing system, and treatment fidelity. Qualitative information will inform any
necessary changes to the program or trial methods before conducting a full-scale trial.
Descriptive statistics will be used to provide means and standard deviations for SPIN-SSLED
Program outcome measures.
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