Type 1 Diabetes Clinical Trial
Official title:
STigma and Its Impact on Glucose Control aMong Youth With diAbetes, a Canada-Wide Study
Stigma related to chronic disease is rejection or judgement or exclusion by others that is
related to the chronic disease itself and is unwarranted. We are trying to figure out what
proportion of young people with type 1 diabetes experience stigma in Canada. By young
people, we mean teenagers and young adults; specifically, people who are between 14 and 25
years of age. This is a challenging period in life when identities are developed and peer
opinions are felt to be particularly important. Experiencing stigma in this life period may
be especially hurtful and may have bad effects on taking care of type 1 diabetes. This may
lead to important medical problems like dangerously low or high blood sugar values. By
understanding how common stigma is, we can figure out the need for programs and strategies
to deal with it.
We will ask young people with type 1 diabetes to help us study this problem by completing an
online survey. We will 'advertise' our study through type 1 diabetes clinics, websites, and
social media. People who are eligible and interested will click on an internet link and be
directed to the survey. Staff at clinics in Montreal, Calgary, and Vancouver will also draw
their attention to the posters and/or provide small flyers with the internet link for the
study.
Participants will be asked about their general sense of well-being, their habits and
behaviours, and their blood sugar control, including frequency of both lows and highs. They
will also be asked if they are willing to mail in a small blood sample. If yes, they will
receive a kit with a small lancing device and instructions on how to clean their finger tip,
prick it, and express a few drops of blood into a small container. They will then mail this
back to us in a postage-paid envelope. We will use this to measure their hemoglobin A1c, an
overall measure of blood sugar control.
We will use this information to (1) calculate the proportion of young people with type 1
diabetes who experience stigma; (2) figure out what factors and behaviours might predict or
signal the experience of stigma; (3) see if there is a link between stigma and A1c control
and/or frequent lows by report; (4) explore challenges and solutions voiced through the
open-ended questions.
Stigma in diabetes has been understudied. Some recent investigations have examined stigma in
adults with type 1 diabetes through in-depth interviews. Such qualitative evaluations
provide important insights into the roots and experiences of stigma, but cannot capture the
prevalence of the problem. This is a key gap that we will address through a national sample.
We will also assess the relationship of stigma to both glycemic control and patient-reported
outcomes (PROs) such as mood, self-efficacy, and sense of well-being. PROs are increasingly
recognized as critical outcome measures. Finally, we will explore potential solutions with
participants.
Methods
1. Selection of questions to capture stigma: As a starting point, we will consider the
questions included by Mulvaney and colleagues in their validated Barriers to diabetes
adherence in adolescents questionnaire. This 21-item tool includes 6 questions on
stigma and 4 other components (stress and burnout, time pressure and planning, social
support, parental autonomy support) and showed good overall internal consistency
(Cronbach's alpha 0.88). We will also consider additional questions proposed by our
team, related to lived experiences with type 1 diabetes and to managing young people
with type 1 diabetes (e.g., stigma within social media networks).
2. Creation of on-line questionnaire Based on (1), we will create an online questionnaire
through FluidSurveys™ (www.fluidsurveys.com). Participants will be able to fill the
survey directly online or offline on tablets, laptops or cell phones. The survey
platform also allows participants to upload documents (pictures, videos, text). The
questionnaires will be available in both French and English and will include
close-ended and open-ended questions. Participants will be allowed to interrupt survey
completion as needed and continue at a later time, as convenient.
In addition to stigma, we will query peer support, quality of life and well-being,
diabetes history and current treatment, and socio-demographic information.Overall
well-being will be assessed with the WHO-5 well being index, a validated 5-item
questionnaire. It is the most widely used questionnaires assessing subjective
psychological well-being and has been used in people with type 1 diabetes. Demographic
factors including age, sex, and ethnocultural background will be queried to ascertain
if the prevalence of diabetes-related stigma is more common in some demographic
subgroups (e.g., teens vs. young adults, females vs. males, ethnocultural groups).
Similarly, we will query sexual orientation/gender identification in order to
ascertain, for example, if being LGBT (i.e., Lesbian, Gay, Bisexual, Transgender), or
subgroups thereof, is associated with higher prevalence of diabetes-related stigma.
Owing to their potentially sensitive nature, however, the questions on sexual
orientation/gender orientation will be explicitly optional
Following completion of close-ended questions, participants will respond to open-ended
questions that seek to capture experiences and perceptions of stigma as well ideas as
to how stigma may be effectively addressed. They will be permitted to upload
explanatory materials (e.g., videos, testimonials, pictures, drawings).
3. Following survey completion, participants will receive a kit for A1c testing
(DTILaboratories, Inc.) with a pre-paid envelope for mailing the sample back to
Montreal. The kit includes a sample vial that contains EDTA preservative, a vial
holder, a single use lancet, a capillary tube device to draw up a small amount of blood
after lancing, and a Ziploc bag. Participants will receive instructions to place the
vial on the vial holder, wash their hands, lance a finger tip (they are familiar with
this, as type 1 diabetes patients), draw up the blood with the capillary tube, and then
release the blood into the vial. The instructions include pictures. They will then
place the vial into the Ziploc bag, then into the prelabelled and postage paid box, and
then mail the package through a Canada Post mail box. The samples are stable for 2.5
months without refrigeration. The AccuBase A1c Test Kit is a non-fasting, finger stick,
whole blood mail-in test requiring a very small blood volume (0.001ml). Samples are
stable for 45 days un-refrigerated once collected. They are analysed using a two step
process. The screening step detects hemoglobin variants and/or disturbed erythrocyte
kinetics by ion-exchange high performance liquid chromatography (HPLC). The second step
includes the use of an interference-free procedure HPLC-boronate affinity, that
provides a hemoglobin A1c value free of possible interferences including chemically
modified derivatives. It is considered one of the most accurate and comprehensive A1c
tests available.
Recruitment Adolescents and emerging adults with type 1 diabetes aged ≥ 14 and < 25 years
will be recruited. The study will be publicized through Facebook©, Twitter© , and other
forms of social media as well as websites of organizations such as Canadian Diabetes
Association, Juvenil Diabetes Research Foundation, Diabète Québec and the Quebec Diabetic
Children's Foundation. These organizations may be asked to mail out flyers or send email
messages through any patient contacts. Specifically, the study will be publicized through
posters at diabetes clinics, Facebook© pages and websites of diabetes organizations and
messages on Twitter©. As in previous studies, we will include a description of the STIGMA
study with a link on the websites of diabetes organizations. We will also ask the
organizations to contact their members directly to inform them about the study, with a link
embedded in the email message.
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