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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00355836
Other study ID # CZH/4/153
Secondary ID
Status Completed
Phase N/A
First received July 24, 2006
Last updated November 4, 2015
Start date November 2004
Est. completion date February 2007

Study information

Verified date November 2015
Source University of Aberdeen
Contact n/a
Is FDA regulated No
Health authority United Kingdom: Research Ethics Committee
Study type Interventional

Clinical Trial Summary

The purpose of this study is to assess the therapeutic benefits of motor imagery training in stroke patients with persistent motor weakness.


Description:

Stroke is a common and highly debilitating illness. Many patients (41-45%) experience chronic motor impairments (Dijkerman et al., 1996) and limitations in activities of daily living (Wade & Langton Hewer, 1987) even after extensive neurological rehabilitation. They often result in long-term dependence at a considerable cost to the carers and the health service. It is therefore crucial to optimise motor recovery after stroke. This study investigates the therapeutic benefits of motor imagery training in stroke patients with a motor weakness.

Evidence for the idea that motor imagery training could enhance the recovery of hand function comes from several separate bases of evidence: the sports literature; neurophysiological evidence; evidence from health psychology research; as well as preliminary findings using motor imagery techniques in stroke patients.

There is evidence to suggest that mental rehearsal of movement can produce effects normally attributed to practising the actual movements. Imagining hand movements could stimulate the redistribution of brain activity, which accompanies recovery of hand function, thus resulting in a reduced motor deficit. Patients are assessed before and after a four-week evaluation period. In this randomised controlled trial 45 patients daily mentally rehearse movements with their affected hand under close supervision. Their recovery is compared to 45 patients who perform closely supervised non-motor mental rehearsal, and 45 patients who are not engaged in a training program.


Recruitment information / eligibility

Status Completed
Enrollment 135
Est. completion date February 2007
Est. primary completion date February 2007
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

Confirmed diagnosis of stroke in the last 1-6 months Persisting upper limb weakness -

Exclusion Criteria:

Alcohol/ Drug abuse Psychiatric history Previous illness that has impacted on individuals Activity of Daily living

- Dementia (assessed by MSQ) Severe Aphasia

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Factorial Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Mental Imagery


Locations

Country Name City State
United Kingdom University of Aberdeen Aberdeen
United Kingdom Ninewells Hospital Dundee

Sponsors (2)

Lead Sponsor Collaborator
University of Aberdeen Chief Scientist Office of the Scottish Government

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Action Research Arm Test (ARAT) (Lyle, 1981)
Secondary Grip strength (dynamometer; Heller et al., 1987),
Secondary Nine hole pegboard task (Mathiowetz et al., 1985, Wade [ref]),
Secondary Function Limitation Profile
Secondary Barthel Index
Secondary Recovery Locus of Control
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