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Evaluation of an Individualised Written Education Package for Stroke Patients

Primary Purpose

Stroke

Status
Completed
Phase
Phase 2
Locations
Australia
Study Type
Interventional
Intervention
'What you need to know about stroke' education package
Sponsored by
Medical Benefits Fund of Australia
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional educational/counseling/training trial for Stroke

Eligibility Criteria

0 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Royal Brisbane Hospital

Outcomes

Primary Outcome Measures

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

Secondary Outcome Measures

Full Information

First Posted
August 2, 2005
Last Updated
August 18, 2005
Sponsor
Medical Benefits Fund of Australia
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1. Study Identification

Unique Protocol Identification Number
NCT00126295
Brief Title
Evaluation of an Individualised Written Education Package for Stroke Patients
Official Title
Evaluation of a Computer-Generated Individualised Written Education Package for Patients Following Stroke and Their Carers
Study Type
Interventional

2. Study Status

Record Verification Date
August 2005
Overall Recruitment Status
Completed
Study Start Date
June 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
May 2005 (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Medical Benefits Fund of Australia

4. Oversight

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke

7. Study Design

Primary Purpose
Educational/Counseling/Training
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
Double
Allocation
Randomized
Enrollment
130 (false)

8. Arms, Groups, and Interventions

Intervention Type
Device
Intervention Name(s)
'What you need to know about stroke' education package
Primary Outcome Measure Information:
Title
knowledge about stroke
Title
self-efficacy
Title
anxiety
Title
depression
Title
perceived health status (patients only)
Title
satisfaction with the content and presentation of the information received
Title
desire for additional information

10. Eligibility

Sex
All
Minimum Age & Unit of Time
0 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Tammy C Hoffmann
Organizational Affiliation
The University of Queensland
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Kryss McKenna
Organizational Affiliation
The University of Queensland
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Linda Worrall
Organizational Affiliation
The University of Queensland
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Stephen Read
Organizational Affiliation
Royal Brisbane Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Brisbane Hospital
City
Brisbane
State/Province
Queensland
ZIP/Postal Code
4029
Country
Australia

12. IPD Sharing Statement

Citations:
PubMed Identifier
34813082
Citation
Crocker TF, Brown L, Lam N, Wray F, Knapp P, Forster A. Information provision for stroke survivors and their carers. Cochrane Database Syst Rev. 2021 Nov 23;11(11):CD001919. doi: 10.1002/14651858.CD001919.pub4.
Results Reference
derived

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Evaluation of an Individualised Written Education Package for Stroke Patients

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