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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00547690
Other study ID # 9179
Secondary ID 0555637Z
Status Terminated
Phase Phase 2
First received October 18, 2007
Last updated June 4, 2012
Start date April 2003
Est. completion date October 2008

Study information

Verified date June 2012
Source University of Kansas Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The primary purpose of the study is to examine the effect of acupuncture treatment when combined with strength training on the motor functional recovery of stroke survivors


Description:

In this study, we compare the effect on motor functional improvement between a combined acupuncture and strength training program and the strength training alone. The results may allow us to determine whether the acupuncture may bring in additional benefit to the motor recovery in the upper limb in stroke survivors


Recruitment information / eligibility

Status Terminated
Enrollment 20
Est. completion date October 2008
Est. primary completion date October 2008
Accepts healthy volunteers No
Gender Both
Age group 20 Years and older
Eligibility Inclusion Criteria:

- After stroke (>6 months)

Exclusion Criteria:

- Other neurological diseases

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Acupuncture and Strengthening
Acupuncture and strengthening
Strengthening Alone
Strengthening training program

Locations

Country Name City State
United States University of Kansas Medical Center Kansas City Kansas

Sponsors (2)

Lead Sponsor Collaborator
Wen Liu, Ph.D. American Heart Association

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fugl-Meyer Motor Scores Before and After 6 Week Treatment No
Secondary Active wrist ROM Before and After 6 Week Treatment No
Secondary Quantitative Measure of Muscle Spasticity Before and After 6 Week Treatment No
Secondary Ashworth Score Before and After 6 Week Treatment No
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