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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02524015
Other study ID # 5150231
Secondary ID
Status Completed
Phase N/A
First received August 7, 2015
Last updated November 17, 2017
Start date September 2015
Est. completion date July 2017

Study information

Verified date November 2017
Source Loma Linda University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this study is to see if a specific physical therapy intervention speeds recovery from stroke-related "pusher syndrome."


Recruitment information / eligibility

Status Completed
Enrollment 8
Est. completion date July 2017
Est. primary completion date July 2017
Accepts healthy volunteers No
Gender All
Age group 21 Years to 89 Years
Eligibility Inclusion Criteria:

- Recent (within 2 months) unilateral stroke

- Burke Lateropulsion Scale = 2

- Age 21 to 89 years

- Ability to provide informed consent

- English-speaking

Exclusion Criteria:

- Prior stroke within the past 6 months

- Cerebellar stroke

- Stroke-related brain imaging (MRI or CT) unavailable

- Global or receptive aphasia

- Prior documented neurologic disorder (e.g., multiple sclerosis, Parkinson's)

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Novel physical therapy

Standard physical therapy


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Loma Linda University

Outcome

Type Measure Description Time frame Safety issue
Primary Recovery from pusher syndrome as measured by changes in the Burke Lateropulsion Scale score over time. The Burke Lateropulsion Scale (BLS) is used in the literature to measure the presence of pusher syndrome. We will measure BLS upon admission and at weekly intervals to monitor whether patients in the experimental group demonstrate faster recovery than the control group, as demonstrated by change in BLS score over change in time (days). Initial, and then weekly until discharge from inpatient rehabilitation unit. Average inpatient stay is expected to be no greater than 4 weeks.
See also
  Status Clinical Trial Phase
Completed NCT03991390 - Effectiveness of Balance Exercise Program for Stroke Patients With Pusher Syndrome N/A
Withdrawn NCT03831594 - Combining Physical Therapy With Vestibular Stimulation to Improve Postural Stability in Pusher's Syndrome N/A
Not yet recruiting NCT05142670 - Task-oriented Training for Patients With Pusher Syndrome N/A