None listed
Conditions
Brief summary
This trial will evaluate a highly accessible and ultra-brief online psychological treatment for women with perinatal depression or anxiety. The treatment involves online materials and optional support from a psychologist. We will evaluate how helpful the treatment has been 2 weeks and then 4 weeks after baseline. All participants will complete questionnaires at baseline, Week 3, and Week 5. We hypothesise that the treatment will lead to reductions in depression and anxiety.
Interventions
This is a single group trial; therefore, all participants will receive access to treatment. The treatment itself consists of a single online lesson which provides psychoeducation about the nature of perinatal anxiety and depression, recommendations for self-management of symptoms, and one week of optional contact with a clinician from the eCentreClinic. This intervention will also include practice exercises, illustrative case examples, and an additional resource on managing worry and problem solving. It is expected that participants will take 60 minutes to read the lesson, read the practice exercises and resource, and read the case stories. Additional skills practice is at the discretion of the participant. The materials consist of PDF and static powerpoint slides. Adherence will be monitored by tracking the number of times a participant has viewed or downloaded each document. The psychologist will contact participants to arrange a telephone call within a week of this lesson being released. Participants will be able to speak over the phone with the psychologist within a week of the participant viewing the lesson (i.e., this contact is not limited to the week that the treatment becomes available to accommodate participant availability). There is no time limit to this telephone consult or private messages, although it is expected that phone consults will be 20-30 minutes long. The purpose of contact is to answer any questions participants may have about the lesson and support them to implement the skills. Additional contact outside this week will be made if participants indicate that they are at risk of suicide/ self-harm or are experiencing technical difficulties.
Sponsors
Study design
Eligibility
Inclusion criteria
(a) Australian woman (b) Aged 18-years or over (c) In the perinatal period (pregnant to 12m postpartum) (d) experiencing depression or anxiety symptoms
Exclusion criteria
(a) Imminently suicidal or unable to keep themselves safe (b) Not living in Australia (c) Unable to read and understand English (d) Displaying significant risk of harming others