Novel Treatment For Pusher Syndrome Using Physical Therapy

Sponsor
Loma Linda University (Other)
Overall Status
Completed
CT.gov ID
NCT02524015
Collaborator
(none)
8
2
22

Study Details

Study Description

Brief Summary

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

Condition or Disease Intervention/Treatment Phase
  • Other: Novel physical therapy
  • Other: Standard physical therapy
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
8 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Outcomes Assessor)
Primary Purpose:
Treatment
Study Start Date :
Sep 1, 2015
Actual Primary Completion Date :
Jul 1, 2017
Actual Study Completion Date :
Jul 1, 2017

Arms and Interventions

Arm Intervention/Treatment
Other: Control

Standard Physical Therapy

Other: Standard physical therapy

Experimental: Intervention

Novel Physical Therapy

Other: Novel physical therapy

Outcome Measures

Primary Outcome Measures

  1. Recovery from pusher syndrome as measured by changes in the Burke Lateropulsion Scale score over time. [Initial, and then weekly until discharge from inpatient rehabilitation unit. Average inpatient stay is expected to be no greater than 4 weeks.]

    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).

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years to 89 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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)

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Loma Linda University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Mary Kim, Assistant Professor, Residency Program Director, PM&R, Loma Linda University
ClinicalTrials.gov Identifier:
NCT02524015
Other Study ID Numbers:
  • 5150231
First Posted:
Aug 14, 2015
Last Update Posted:
Nov 21, 2017
Last Verified:
Nov 1, 2017
Keywords provided by Mary Kim, Assistant Professor, Residency Program Director, PM&R, Loma Linda University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 21, 2017