Obesity Clinical Trial
Official title:
Multicomponent Risk Factor Intervention for People With a Severe Mental Illness: a Feasibility Study
This study is a feasibility study of a multi-component intervention to enhance healthy living among young people with psychotic disorders, specifically targeting smoking and weight.
We propose a feasibility study of a multi-component intervention to enhance healthy living
among young people (18 to 40 years) with psychotic disorders, specifically targeting smoking
and weight. Smoking is very common amongst people with psychotic disorders (around 70% of
males, and over 50% of females) and this adds to the overall cardiovascular risk for this
group. Obesity is also a common problem for people with psychosis, with an estimated 40-60%
being obese or overweight. Obesity in this population may contribute to adverse medical and
psychological consequences. For many obese people, targeted pharmacotherapy in addition to
diet and increased physical activity can assist in both weight reduction and the maintenance
of gains. Similarly, smoking cessation is enhanced by use of adjunctive medications such as
nicotine replacement; such strategies continue to produce abstinence rates for up to 10
years.
The proposed study will assess the feasibility of a multi-component behavioural intervention
focussing on smoking cessation/diet/physical activity.
The primary outcome measures from the feasibility study are smoking cessation and reduction
in body mass index (BMI). Secondary outcomes will include tolerability and safety, as well
as the impact the package has on other cardiovascular risk factors including serum lipids,
blood sugar levels and depression in young people with psychosis. We will also establish
whether smoking cessation and reduction in obesity is correlated with gains in terms of body
image, quality and enjoyment of life and reduction in depression. Based on published data,
behavioural interventions for smoking cessation and diet and physical activity lead smoking
cessation in 20% of people at 12 months and to modest weight loss (around 5%).
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Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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