Food Allergy Clinical Trial
Official title:
To What Extent do Social Cognition Models Explain Adherence to Self-care Regimens in Adolescents and Young Adults With Food Allergy
Anaphylaxis is a severe and potentially life threatening allergic reaction which can affect
the airway, breathing and/or circulation. This reaction can be triggered by a number of
different allergens but the most common are food, medications, insect venom and latex.
Because these reactions occur suddenly and are potentially very serious, the best management
lies in the correct use of the prescribed emergency medication. Epinephrine, or adrenaline
as it is more commonly known, is the recommended drug for the treatment of anaphylaxis.
Injecting the epinephrine into the outer thigh muscle is the preferred route of
administration. For health professionals, patients and carers, this rapid administration is
facilitated by the manufacture of preloaded syringes and autoinjectors. Despite the
availability of these devices, a review of studies shows poor knowledge and skills amongst
both health professionals and patients with regards to using autoinjectable epinephrine
devices correctly. These studies found that as well as poor knowledge in using the
autoinjectors, there was a lack of confidence amongst patients and an unwillingness to carry
the device with them at all times.
In other disease groups like asthma and diabetes, psychological models which involve asking
people how they think about their illness and their related behaviours, have been found to
help in the understanding of why some people follow or adhere to health professionals advice
and why others do not. Based on these findings, this study will look at two appropriate
psychological models and their ability to predict variation in adherence to self-care
regimens in adolescents and young adults with food allergy related anaphylaxis.
Study Design: Cross-sectional comparison of the Self Regulatory Model (Leventhal, 1984) and
The Health Belief Model (Rosenstock, 1966) by which the models will be used to predict and
understand adherence to selfcare regimens of adolescents and young adults with food allergy.
Proposed Sample Size / Power Calculations:
The power calculation was based on multiple regression analysis for all predictor variables,
25 in total. To predict a minimum of 10% of the variance in adherence with an alpha=0.05 and
power=0.90, a minimum proposed sample size of 275 participants will be needed. A 40%
attrition rate has been anticipated due to the use of postal questionnaires and so a minimum
of 459 participants will need to be recruited.
Analyses Nonparametric item response theory analysis, univariate correlations and
multiregressional analysis for predictor models will be conducted. Structural equation
modelling will also be applied to assess the goodness of fit of the two social cognition
models.
Setting This study will be based in an outpatients setting and in the community.
Participants will be identified and recruited from their hospital allergy clinic either
whilst attending an appointment or from a hospital mail out. The third method of recruitment
will involve participants from a convenience sample of the universities of Sussex and
Brighton.
Procedure Phase 1 Recruitment and consent The recruitment of study participants will involve
three methods. The first method will involve recruiting participants in person from their
hospital allergy clinic. Eligible individuals identified by clinic staff will be given a
participant information leaflet and asked if they are interested in taking part in the
study. Once verbal consent is given, participants will be directed to the chief investigator
who will be present in clinic. Interested individuals would then have the opportunity to
discuss the research with the chief investigator and/or the clinic staff. If still
interested, individuals (aged 16-21 or parents of those aged 13-15) will be asked to sign
two consent forms (one copy to keep for themselves) and be given a questionnaire. The
participants will be given the opportunity to complete the questionnaire within the clinic,
or take it home to complete. If the latter option is chosen, a freepost envelope addressed
to the research team will be provided. Participants will also be given a correspondence slip
on which to write their contact details to return separately to the research team if they
are interested in receiving a summary of findings.
The second method of recruitment will involve a patient database search by clinic staff and
subsequent mail out to eligible individuals. Clinic staff will search their patient records
for individuals who fit the inclusion criteria. The consultant in charge will confirm their
eligibility and sign the invitation letter prepared on hospital headed paper. This will be
put in an envelope together with the participant information leaflet, two consent forms (one
copy for the participant to keep and the other to be returned), the questionnaire, future
correspondence slip and freepost envelope addressed to the research team.
The third method of recruitment will be a convenience sample through the Universities of
Sussex and Brighton. A generic email will be sent to staff and students consisting of the
participant information leaflet and detailing the main inclusion criteria. Individuals who
are eligible and interested in taking part in the research will be asked to reply to the
email with their contact details. Similarly to those recruited from the clinic mail out,
these participants will be sent a pack containing another participant information leaflet,
two consent forms, a questionnaire, a correspondence slip and a freepost envelope addressed
to the research team.
Phase 2 - Questionnaire In order to measure the models, carefully constructed and piloted
questionnaires have been developed. Each participant will be asked to complete one
questionnaire on one occasion. The questionnaire will collect demographic details, assess
knowledge of how and when to use medication, confidence in the individual's own ability to
use the medication, management of food allergy, the Revised Illness Perception Questionnaire
(Moss-Morris et al., 2002) which is the validated questionnaire to measure items from the
Self-Regulatory Model (Leventhal, 1984), items which relate to factors found within the
Health Belief Model (Rosenstock, 1966) and finally the Revised Life Orientation Test
(Scheier et al., 1994). The questionnaire completion time has been confirmed with
individuals within the targeted age range and is expected to take no longer than 40 minutes
to complete. In order to improve the response rate of questionnaires, a second mail out will
be sent to all eligible participants one month after the initial mail out.
Phase 3 - Feedback to participants Those participants who expressed an interest in receiving
a summary of findings and provided contact details will be sent a summary document upon
completion of the study.
Measures Demographic/background Participants will be asked their age, gender, ethnicity,
size of family, history of food allergy and anaphylaxis, use of the emergency medication
autoinjectable epinephrine, membership of an allergy support group, possession of a
management plan for their food allergy.
Knowledge Knowledge about how and when to use an autoinjectable epinephrine device will be
measured and the individuals confidence in their ability to do so correctly will also be
looked at. This will enable us to explore whether underuse is as a result of poor knowledge
or whether this can be better explained by other factors.
Adherence Adherence will be measured by asking participants about their current methods of
managing their food allergy. This will include questions on allergen avoidance and carrying
emergency medication (auto-injectable epinephrine and additional medicines they may use to
treat their food allergy).
Revised Illness Perception Questionnaire (Moss-Morris et al., 2002), Health Belief Model
(Rosenstock, 1966) items and the Revised Life Orientation Test (Scheier et al., 1994) The
Revised Illness Perception Questionnaire (Moss-Morris et al., 2002) measures constructs from
the Self-Regulatory Model (Leventhal, 1984) which include symptoms, the duration of food
allergy, the consequences of having food allergy, the personal control an individual feels
they have over their food allergy, the amount the individual feels the treatment can control
their food allergy, emotions they associate with their food allergy, how much they
comprehend their food allergy and what they believe are the causes. The Health Belief Model
(Rosenstock, 1966) similarly looks at attitudes but in this case how susceptible and serious
individuals feel suffering an allergic reaction would be, the barriers and benefits to
following recommended advice and what prompts these individuals to follow this advice. The
Revised Life Orientation Test (Scheier et al., 1994) will also be measured to determine
levels of optimism which has been found in other studies to impact on the way participants
respond to items on questionnaires.
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Time Perspective: Cross-Sectional
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