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Effects of early motivational interviewing on post-stroke depressive symptoms: a pilot randomised controlled trial of the Good Mood Intervention program.

Effects of early motivational interviewing on post-stroke depressive symptoms: a pilot randomised controlled trial of the Good Mood Intervention program.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12617000245392
Acronym
Good Mood Study
Enrollment
34
Registered
2017-02-17
Start date
2013-09-13
Completion date
2014-08-14
Last updated
2017-02-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

Depression is a frequent consequence of stroke that affects recovery adversely and can lead to greater mortality; however, it is often undetected or treated inadequately. While antidepressants can be used to treat post-stroke depression (PSD), they increase the risk of side-effects which complicate recovery. This randomised controlled trial evaluates a new brief intervention, the Good Mood Intervention program. The aim of the study is to investigate if motivational interviewing (MI) improves patients’ mood post-stroke. It will be conducted at the Stroke Unit, Western Hospital, Melbourne and will recruit inpatients with acute stroke.

Interventions

Intervention group patients will receive early motivational interviewing (MI), provided by facilitators (nurses or social workers) during the acute in-patient hospitalisation after presentation with stroke. Facilitators will have completed a full-day workshop and completed an online training module. MI will comprise 3, 30-minute individual sessions, performed prior to hospital discharge from the acute episode.. Generally, the sessions will occur on 3 separate and consecutive days. The rationale

Intervention group patients will receive early motivational interviewing (MI), provided by facilitators (nurses or social workers) during the acute in-patient hospitalisation after presentation with stroke. Facilitators will have completed a full-day workshop and completed an online training module. MI will comprise 3, 30-minute individual sessions, performed prior to hospital discharge from the acute episode.. Generally, the sessions will occur on 3 separate and consecutive days. The rationale for using multiple sessions is (a) due to the complexity of the problems of stroke and depression, and (b) there is a significant positive relationship between the amount of MI a person receives and treatment outcomes. A summary of the 3 sessions follows: 1: Setting agenda and encouraging patient to talk about adjustment to stroke; 2: Eliciting realistic goals for recovery, and barriers to achieving goals; and, 3: Identifying ambivalence about achieving goals; supporting patient’s optimism and self-efficacy, and identifying solutions to problems. Fidelity will be assessed for all facilitators on an individual basis after review of recorded interviews. Further training will be provided for facilitators who do not demonstrate appropriate technique for MI.

Sponsors

Debra Kerr
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

acute presentation after an acute stroke (cerebral infarction/intracerebral haemorrhage); cognitively alert; aged 18 years and over; patients who could speak and read English.

Exclusion criteria

subarachnoid haemorrhage; subdural haematoma; severe cognitive/communication problems such as significant dysphasia or aphasia; mental health conditions including depressive symptoms requiring professional support one month prior to stroke; concurrent neurological disease/trauma; and, myocardial infarction.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026