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Evaluation of an Individualised Written Education Package for Stroke Patients

Evaluation of a Computer-Generated Individualised Written Education Package for Patients Following Stroke and Their Carers

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00126295
Enrollment
130
Registered
2005-08-03
Start date
2003-06-30
Completion date
2005-05-31
Last updated
2005-08-19

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

Conditions

Stroke

Brief summary

The primary aim of the randomised controlled trial was to evaluate the effectiveness of a tailored written education package (What you need to know about stroke) on the outcomes of: * Knowledge about stroke, self-efficacy, anxiety, depression, perceived health status, satisfaction with the content and presentation of the information received, and desire for additional information for patients following stroke and * Knowledge about stroke, self-efficacy, anxiety, depression, satisfaction with the content and presentation of the information received, and desire for additional information for their carers. A secondary aim was to evaluate the effect of written information on the outcomes of knowledge about stroke, self-efficacy, anxiety, depression, and perceived health status of patients following stroke and on knowledge about stroke, self-efficacy, anxiety, and depression of their carers.

Interventions

DEVICE'What you need to know about stroke' education package

Sponsors

Medical Benefits Fund of Australia
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
ECT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
0 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Had a stroke or transient ischemic attack (TIA) or was the informal carer of a person who had a stroke or TIA; * Had a reported English-proficiency level, corrected hearing and vision, and communication status adequate to participate in an interview and complete assessment tasks; * Did not have reported or observable dementia; * Lived within 50km of the hospital, for ease of follow-up; and * Was medically stable.

Design outcomes

Primary

MeasureTime frame
knowledge about stroke
self-efficacy
anxiety
depression
perceived health status (patients only)
satisfaction with the content and presentation of the information received
desire for additional information

Countries

Australia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026