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Improving outcome after stroke

imProving Outcome after Stroke (POST) A simple intervention to improve psychological outcomes

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12608000311358
Acronym
POST
Enrollment
201
Registered
2008-06-30
Start date
2008-09-09
Completion date
2010-07-06
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

AIMS: The primary aim of this project is to determine if a simple intervention (a personalised postcard, sent monthly) improves psychosocial outcomes in patients with a recent stroke. The secondary aim is to determine appropriate outcome measures and potential mechanisms of action for a large, multi-centre, randomized controlled trial in patients surviving stroke. RESEARCH PLAN: This is a single-centre (Gosford Hospital Stroke Service), randomized, double-blind pilot/proof of concept trial of a simple intervention to improve psychosocial outcomes in patients with a recent (within 8 weeks) stroke.

Interventions

Intervention: 1 personalised postcard, sent once a month (in an envelope) for 5 months following discharge from hospital. Participants will consent to a baseline screening assessment and interview, and contact from research staff for a period of up to six months following hospital discharge to determine their outcome and factors that might improve recovery. Specific information is archived on this site but not available for the general public to maintain blinding to treatment allocation and prim

Intervention: 1 personalised postcard, sent once a month (in an envelope) for 5 months following discharge from hospital. Participants will consent to a baseline screening assessment and interview, and contact from research staff for a period of up to six months following hospital discharge to determine their outcome and factors that might improve recovery. Specific information is archived on this site but not available for the general public to maintain blinding to treatment allocation and primary hypothesis.

Sponsors

National Stroke Foundation
Lead SponsorCharities/Societies/Foundations

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Prevention
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to 120 Years
Healthy volunteers
No

Inclusion criteria

Recent (within 8 weeks) stroke; Non-depressed (<8 on Hospital Anxiety and Depression Scale depression subscale at baseline - HADS); Fixed address in NSW; Sufficient English to respond to study questions; Able to provide informed consent.

Exclusion criteria

Depressed at baseline (scoring 8 or more on the HADS depression subscale)

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026