Journal Article

A cluster randomized controlled trial of an online psychoeducational intervention for people with a family history of depression

Levitan, Charlene, Mills, Llewellyn, Ahmad, Raghib, Peate, Michelle, Mitchell, Philip B., Barlow-Stewart, Kristine, Dunlop, Kate, Dobbins, Timothy, Sherman, Kerry A., Meiser, Bettina, Schofield, Peter R., Trevena, Lyndal, Christensen, Helen

2019

Overview

Background People with a family history of major depressive disorder (MDD) or bipolar disorder (BD) report specific psychoeducational needs that are unmet by existing online interventions. This trial aimed to test whether an interactive website for people at familial risk for depression (intervention) would improve intention to adopt, or actual adoption of, depression prevention strategies (primary outcome) and a range of secondary outcome measures. Methods In this cluster randomised trial, primary care practises were randomised to either provide the link to the intervention or the control website. Primary health care attendees were invited by letter to opt into this study if they had at least one first-degree relative with MDD or BD and were asked to complete online questionnaires at baseline and 2-week follow-up. Results Twenty general practices were a randomized, and 202 eligible patients completed both questionnaires. Thirty-nine (19.3%) of participants were male and 163 (80.7%) female. At follow-up, compared to controls, the intervention group: (i) were more likely to intend to undergo, or to have actually undergone, psychological therapies (OR = 5.83, 95% CI: 1.58–21.47, p  = .008); (ii) had better knowledge of depression risk factors and prevention strategies (mean difference = 0.47, 95% CI: 0.05–0.88, p  = .029); and (iii) were more likely to accurately estimate their lifetime risk of developing BD (mean difference = 11.2, 95% CI: -16.52– -5.73, p  < .001). There were no statistically significant between-group differences in change from baseline to follow up for any of the remaining outcome measures (Patient Health Questionnaire, Perceived Devaluation-Discrimination Questionnaire and Perceived Risk of Developing MDD). Conclusion The opt-in nature of the study may have led to participation bias, e.g. underrepresentation of males, and hence may limit generalisability to the broader population at familial risk for depression. This is the first website internationally focusing specifically on informational needs of those at familial risk of depression. Our interactive website can play an important role in improving the outcomes of individuals at familial risk for depression. Testing the intervention in other settings (e.g. psychology, psychiatry, genetic counselling) appears warranted. Trial registration The study was prospectively registered with the Australian and New Zealand Clinical Trials Group (Registration no: ACTRN12613000402741 ).

• Publisher: BioMed Central,BioMed Central Ltd,Springer Nature B.V,BMC
• Subject: Adolescent / Adult / Aged / Analysis / Australia - epidemiology / Bipolar disorder / Clinical trials / Depression (Mood disorder) / Depressive Disorder, Major - epidemiology / Depressive Disorder, Major - psychology / Depressive Disorder, Major - therapy / Education / Evidence-based medicine / Family / Family history / Family medicine / Female / General practitioners / Genetic counseling / Genetic research / Health risk assessment / Health surveys / Humans / Internet / Major depressive disorder / Male / Medical genetics / Medical History Taking - methods / Medicine / Medicine & Public Health / Mental depression / Mental disorders / Middle Aged / Mood disorders / New Zealand - epidemiology / Online education / Online intervention / Online Systems / Patient Education as Topic - methods / Patient Health Questionnaire / Prevention / Primary health care / Primary Health Care - methods / Psychiatry / Psycho-education / Psychology / Psychotherapy / Research Article / Risk factors / Statistical analysis / Therapy, Computer-Assisted - methods / Web sites (World Wide Web) / Websites / Young Adult