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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01662960
Other study ID # HN 4404
Secondary ID NIH R01 HD068565
Status Completed
Phase N/A
First received
Last updated
Start date September 7, 2012
Est. completion date February 27, 2017

Study information

Verified date June 2020
Source Albert Einstein Healthcare Network
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the study is to determine whether an existing treatment for problems that participants have with making movements after a stroke can be performed at home.


Description:

This study will compare two forms of home-based treatment for post-stroke problems making movements with the arms and hands. After initial pre-treatment assessments, participants will complete 4 weeks of treatment, with assessments after each week of treatment and 3 months after the completion of treatment.


Recruitment information / eligibility

Status Completed
Enrollment 72
Est. completion date February 27, 2017
Est. primary completion date February 27, 2017
Accepts healthy volunteers No
Gender All
Age group 21 Years to 85 Years
Eligibility Inclusion Criteria:

- 6 months or more post-stroke

- upper extremity Fugl-Meyer score between 10 and 50

- no longer participating in upper-extremity physical or occupational therapy

- sufficient comprehension ability to understand instructions

Exclusion Criteria:

- previous head trauma, psychiatric illness or chronic exposure to medications that might be expected to have lasting consequences for the central nervous system (e.g., haloperidol, dopaminergics)

- dementia

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Mirror therapy
A home-based therapy involving mirrored visual feedback
Divider therapy
A home-based therapy involving removed visual feedback.

Locations

Country Name City State
United States Einstein Medical Center Elkins Park Elkins Park Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Albert Einstein Healthcare Network

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Upper Extremity Fugl-Meyer This test measures impairment-level ability to move the arm and hand. Scores range from 0 to 66, with higher scores indicating greater ability to move the arm and hand. Immediately after 1 month of treatment
Primary Action Research Arm Test The test measures the ability to complete simulated everyday tasks with the arm. Scores range from 0 to 54, with higher scores indicating better performance. 1 month
Primary Rivermead Assessment of Somatosensory Performance This test measures the integrity of sensory perception of the arm. The score is the proportion of items answered correctly, and ranges from 0 to 1 with higher scores indicating better performance. 1 month
Primary Virtual-reality Assessment of Navigation This test measures the ability to detect lateralized attention problems in a simulated navigation test. Evidence for lateralized attentional problems was defined as a 20% difference in item detection between the left and right side. 1 month
Secondary Stroke Impact Scale This test measures the self-reported ability to complete everyday tasks with the arm. Total scores for all items are reported. The scale ranged from 0 to 300, with higher scores indicating higher self-reported ability. 1 month
Secondary Wolf Motor Function Test The test measures the ability to completed simulated everyday tasks with the arm. The scale ranged from 0 to 75, with higher scores indicating better performance. 1 months
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