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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00184431
Other study ID # SU01-ISM-NTNU
Secondary ID
Status Completed
Phase N/A
First received September 15, 2005
Last updated October 17, 2011
Start date April 2004
Est. completion date April 2008

Study information

Verified date October 2011
Source Norwegian University of Science and Technology
Contact n/a
Is FDA regulated No
Health authority Norway: Norwegian Social Science Data Services
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate whether additional task specific physiotherapy treatment and a self administrated home training program results in better balance compared to traditional follow up care.


Description:

Increased risk of falling is a major problem after stroke and impaired balance is one of the main reasons for falling. Early and intensive physiotherapy seems to be beneficial for functional outcome after stroke although it is still unknown whether one specific physiotherapy technique is better than another.

Comparison: Traditional follow up care by the community health care system with additional task specific physiotherapy three times a week and a daily self administrated home training program compared to traditional follow up care by the community health care system.


Recruitment information / eligibility

Status Completed
Enrollment 62
Est. completion date April 2008
Est. primary completion date April 2008
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- Admitted to the stroke unit with a diagnosis of stroke

- Living in the city of Trondheim

- Included 4 - 14 days after first sign of symptoms

- Modified Rankin Scale > 3 before admission to hospital

- Scandinavian Stroke Scale (SSS) less than 58 points and more than 14 points

- SSS leg item less than 6 points or SSS movement item less than 12 points

- Discharged to home or a rehabilitation clinic

- Mini Mental State Examination Score more than 20 points

- Able and willing to provide informed consent

Exclusion Criteria:

- Seriously heart- and lung-diseases

- Other diseases which makes it difficult to evaluate the function

- Already included in the trial

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Physical therapy technique and exercises
The experimental group receives task specific physical therapy three times a week for the first four weeks after discharge from hospital and one session pr week for the next eight weeks in addition to ordinary physical therapy The active comparator group receives only ordinary physical therapy during this period.

Locations

Country Name City State
Norway Norwegian University of Science and Technology Trondheim

Sponsors (3)

Lead Sponsor Collaborator
Norwegian University of Science and Technology Norwegian Fund for Postgraduate Training in Physiotherapy, St. Olavs Hospital

Country where clinical trial is conducted

Norway, 

References & Publications (1)

Askim T, Mørkved S, Engen A, Roos K, Aas T, Indredavik B. Effects of a community-based intensive motor training program combined with early supported discharge after treatment in a comprehensive stroke unit: a randomized, controlled trial. Stroke. 2010 Au — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary The Berg Balance Scale Inclusion, four weeks follow-up, twelve weeks follow-up and six months follow-up No
Secondary Mini Mental State Examination Inclusion No
Secondary Scandinavian Stroke Scale Inclusion No
Secondary Motor Assessment Scale Inclusion, four weeks follow-up, twelve weeks follow-up, six months follow-up No
Secondary Timed Up and Go Inclusion, four weeks follow-up, twelve weeks follow-up, six months follow-up No
Secondary Step Test Inclusion, four weeks follow-up, twelve weeks follow-up, six months follow-up No
Secondary Walking speed Inclusion, four weeks follow-up, twelve weeks follow-up, six months follow-up No
Secondary Barthel Index Inclusion, four weeks follow-up, twelve weeks follow-up, six months follow-up No
Secondary Modified Rankin Scale Inclusion, four weeks follow-up, twelve weeks follow-up, six months follow-up No
Secondary Fall Efficacy Scale Inclusion, four weeks follow-up, twelve weeks follow-up, six months follow-up No
Secondary Stroke Impact Scale Inclusion, four weeks follow-up, twelve weeks follow-up, six months follow-up No
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