Journal of Medical Internet Research - International Scientific Journal for Medical Research, Information and Communication on the Internet #Preprint #PeerReviewMe: Warning: This is a unreviewed preprint. Readers are warned that the document has not been peer-reviewed by expert/patient reviewers or an academic editor, may contain misleading claims, and is likely to undergo changes before final publication, if accepted, or may have been rejected/withdrawn. Readers with interest and expertise are encouraged to sign up as peer-reviewer, if the paper is within an open peer-review period. Please cite this preprint only for review purposes or for grant applications and CVs (if you are the author). Background: Depressive symptoms are common in people with type 2 diabetes and exacerbate disease burden through increased social and occupational impairment and greater morbidity and mortality. Effective depression treatments exist, however rates of depression screening in type 2 diabetes are variable, access to psychological support is characteristically low, and impact of treatment on daily functioning remains unclear. Web-based cognitive behaviour therapy (CBT) is easily accessible, private, non-stigmatising and a potential solution to reducing the substantial personal and public health impact of comorbid type 2 diabetes and depression. Objective: To evaluate the efficacy of the web-based CBT program, myCompass, for improving social and occupational functioning in a large community sample of people with type 2 diabetes and self-reported mild-to-moderate depressive symptoms. myCompass is an unguided, public health treatment program for common mental health problems. Impact of treatment on depressive symptoms, diabetes-related distress, anxiety symptoms and self-care behaviour was also examined. Methods: Participants with type 2 diabetes and mild-to-moderate depressive symptoms (N = 780) were recruited online and via community and general practice settings. Screening, consent and data collection were conducted online, and randomisation was to either myCompass (n = 391) for 8 weeks plus a 4-week tailing off period, or an active placebo intervention (n = 379). At baseline and post-intervention (3-months), participants completed the Work and Social Adjustment Scale (WSAS), the primary outcome measure. Secondary outcome measures included the Patient Health Questionnaire-9 item (PHQ-9), Diabetes Distress Scale (DDS), Generalised Anxiety Disorder Questionnaire-7 item (GAD-7) and items from the Self-Management Profile for Type 2 Diabetes (SMP-T2D). Results: At baseline, mean scores on several outcome measures, including the primary outcome of work and social functioning, were near to the normal range, despite a varied and extensive recruitment process. Of the 780 trial participants, 473 (61%) completed the post-intervention assessment. Intention-to-treat analyses revealed improvement in functioning, depression, anxiety, diabetes distress and healthy eating over time in both groups. Except for blood glucose monitoring and medication adherence, there were no specific between-group effects. Follow-up analyses suggested the outcomes did not depend on age, morbidity or treatment engagement. Conclusions: Improvement in social and occupational functioning and the secondary outcomes was generally no greater for myCompass users than users of the control program at 3 months post-intervention. These findings should be interpreted in light of near-normal mean baseline scores on several variables, the self-selected study sample and sample attrition. Further attention to factors influencing uptake and engagement with mental health treatments by people with type 2 diabetes, and the impact of illness comorbidity on patient conceptualisation and experience of mental health symptoms, is essential to reduce the burden of type 2 diabetes. Clinical Trial: ACTRN12615000931572