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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01134796
Other study ID # 09103
Secondary ID
Status Terminated
Phase N/A
First received May 28, 2010
Last updated December 1, 2015
Start date September 2010
Est. completion date September 2014

Study information

Verified date December 2015
Source University of Nottingham
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Medicines and Healthcare Products Regulatory Agency
Study type Observational

Clinical Trial Summary

Assessment of a custom made grasp device in the rehabilitation of stroke victims.


Recruitment information / eligibility

Status Terminated
Enrollment 10
Est. completion date September 2014
Est. primary completion date September 2014
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

1. Damage to the following areas of the brain, all of which may be involved in coordination of reach to grasp confirmed by CT scan: parietal, cerebellar, internal capsule and basal ganglia,

2. A score of 6 or more on the arm section of the Rivermead Motor Assessment (able to reach and pick up a tennis ball and release on thigh),

3. Time between start of hand opening and start of hand transport > 60 ms (measured with GRASP).

Exclusion Criteria:

1. Cognitive dysfunction which prevents understanding of the task,

2. Severe concurrent medical problems that prevent repetitive reaching (including shoulder pain),

3. A diagnosis of Parkinson's disease, or

4. Lack of informed consent.

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Nottingham

Outcome

Type Measure Description Time frame Safety issue
Primary Time to grasp Primary outcome measures are: 1) The time elapsed between the start of grasp (when the finger breaks contact with the thumb) and the start of transport (when the wrist leaves the start position); and 2) The time elapsed between maximum aperture of the hand and peak deceleration of the wrist. Secondary outcome measures are: 1) movement duration, 2) time of maximum aperture expressed as % of movement duration, 3) time of peak deceleration expressed as % of movement duration, 4) amplitude of peak velocity of the wrist, 5) time of peak velocity, 6) time of peak velocity of the wrist expressed as % movement duration, 7) size of maximum aperture, 8) time to close hand from time of maximum aperture, 9) distance to target at time of maximum aperture. 3 sessions No
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