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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00286702
Other study ID # HEC 01/166
Secondary ID
Status Completed
Phase N/A
First received February 1, 2006
Last updated February 1, 2006
Start date October 2002
Est. completion date September 2004

Study information

Verified date January 2006
Source University of Western Sydney
Contact n/a
Is FDA regulated No
Health authority Australia: Australian Human Research Ethics Committee (NHMRC)
Study type Interventional

Clinical Trial Summary

After a stroke, many people develop contracture of the muscles in their affected wrist and hand which leads to a permanently clenched, painful hand. A contracture is often treated by therapists who use hand splinting to prevent it occurring or slow down its progression. Despite their wide use, there has not been research completed to investigate whether or not splinting prevents contracture in people following stroke. In fact, this project will be the first of its kind in the world and is therefore vital to stroke rehabilitation.

The study is a multi-centre, randomised controlled trial that will measure the effect of hand-splinting in two positions on the prevention of contracture, functional use of the hand, and quality of life.


Recruitment information / eligibility

Status Completed
Enrollment 63
Est. completion date September 2004
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- first ever stroke

- score of <1 on Motor Assessment Scale item 6

Exclusion Criteria:

- comorbidity resulting in previous contracture of the wrist/hand

Study Design

N/A


Related Conditions & MeSH terms


Intervention

Device:
hand splint


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Western Sydney
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