Abstract
to improve long‐term disease control and health‐related quality of life for people with psoriasis, a translational gap of implementing evidence‐based guidelines into practice exist.1 Although behavioural and psychological risk factors are modifiable, empirical support for how to achieve this in practice is lacking. Furthermore, whether this impacts positively on health outcome is not yet established.2 3 The common sense self‐regulation model (CS‐SRM) provides a conceptual framework showing how patient beliefs about health and illness drive their emotional and behavioural responses.
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