Eating Disorders in Adolescence Clinical Trial
Official title:
Social Information Processing in Adolescents With Eating Disorders: Implications for Theory and Clinical Practice
This research project aims to examine whether adding an online programme of cognitive
training exercises may be a helpful addition to treatment as usual for young people with
eating disorders. The cognitive training exercises aim to modify distortions in attention and
thinking during hypothetical, ambiguous social interactions involving the risk of social
rejection.
All participants will complete a baseline assessment consisting of a battery of
questionnaires and computerised tasks, to assess attention and thinking during ambiguous
social interactions involving the risk of social rejection. Participants who display
distortions in attention and thinking will then be randomised to one of two groups. In one
group participants will receive the computerised training alongside their usual treatment. In
the other group participants will continue to receive their treatment as usually only.
Healthy controls will also be invited to take part in the baseline assessment to allow for
comparisons between clinical and non-clinical groups.
The aim of this study is to assess the effects of adding 10 sessions of Cognitive Bias
Modification (CBM) training, and goal planning using implementation intentions, to treatment
as usual for adolescents with eating disorders. It is hypothesised that at baseline,
participants will demonstrate cognitive biases in their attention towards rejecting/critical
facial expressions (attentional bias), and in making negative resolutions of ambiguous social
scenarios involving the risk of social rejection (interpretation bias).
Young people receiving treatment for eating disorders will be recruited from participating
child and adolescent eating disorder services in the United Kingdom. Information about the
study, the main eligibility criteria and contact details for the researcher will also be
advertised using flyers and social media platforms. Individuals from the community who
express an interest in taking part will be screened using the Structured Clinical Interview
for DSM-5 (SCID-5) disorders to screen for psychiatric disorders to determine their
eligibility. Parental consent will be obtained for any participants under the age of 16.
Eligible participants will be invited to meet the researcher for an initial visit, to provide
consent and complete the baseline assessments. The baseline assessments will consist of a
battery of questionnaires used to assess interpersonal sensitivity, mood, anxiety and eating
disorder psychopathology, and computerised tasks to measure various aspects of social
cognition including attention and interpretation biases.
Following the baseline assessments, participants displaying attention and interpretation
biases will be invited to take part in the next phase of the study. Participants randomised
to receive the computerised training will meet with the researcher for a second visit, during
which they will learn how to complete the training tasks, complete the first set of training
modules and create plans involving exposure to the risk of social rejection with the
researcher using the implementation intentions approach. Participants will be asked to
complete the remaining training three times per week over three weeks (10 sessions in total)
and will have weekly contact with the researcher to review adherence to planned behaviours
using implementations intentions. Attention and interpretation biases will be assessed again
at the end of the 3-week training and at 12 weeks follow-up. Questionnaire measures of
interpersonal sensitivity, anxiety, depression and disorder psychopathology will also be
administered at these two time points.
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