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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02190734
Other study ID # Pusher1
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 2014
Est. completion date December 2017

Study information

Verified date April 2019
Source Shirley Ryan AbilityLab
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Some individuals demonstrate pushing behaviors after having a stroke. The purpose of this study is to see if there are immediate changes in pushing behaviors in individuals who have had a stroke before and after sitting in a wheelchair, walking on the treadmill, and walking overground.

The investigators do not think there will be a change with sitting in the wheelchair, but the investigators think there may be an improvement in pushing behaviors after walking training.


Description:

The study population of interest is primarily individuals in inpatient rehabilitation.


Recruitment information / eligibility

Status Completed
Enrollment 6
Est. completion date December 2017
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years to 89 Years
Eligibility Inclusion Criteria:

- score >0 in each subsection of the Scale for Contraversive Pushing

- admitted to the Rehabilitation Institute of Chicago inpatient rehabilitation setting

- stroke within previous 180 days

- consent to participate in the study

- ambulating greater than 150' at a time prior to stroke

Exclusion Criteria:

- other neurologic diagnoses

- weight bearing precautions, orthopedic injuries, or other medical co-morbidities that prevent adherence to the study protocol

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Sitting in wheel chair
Placebo/control intervention- No treatment, sitting in a wheelchair for 30 minutes
Gait training on treadmill
Walking on a treadmill with or without body weight support during 30 minute treatment
Gait training overground
Walking overground with or without body weight support during 30 minute treatment

Locations

Country Name City State
United States Rehabilitation Institute of Chicago Chicago Illinois
United States Rehabilitation Hospital of the Pacific Honolulu Hawaii

Sponsors (1)

Lead Sponsor Collaborator
Shirley Ryan AbilityLab

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Burke Lateropulsion Scale Clinical measure of pushing behaviors in supine, sitting, standing, walking, and transfers will be performed before and after each 30 minute training session. Before and after each of 3 treatment sessions (3 separate days) over a maximum of a 10 day period
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