The Influences of Watching a Movie Clip of Normal Walking on Measurable Walking Parameters Among Post-Brain-Stroke Patients as Opposed to the Influences of a Control Movie Clip Showing Backwards Walking

Hadassah Medical Center

Status and phase: Unknown; Phase 2

Conditions: Stroke

Treatments: Other: watching walk backward clip; Other: watching a normal walking clip

Study type: Interventional

Funder types: Other

Identifiers

NCT00983450

0303-09-HMO

Details and patient eligibility

About

The study will include 20 subjects who will be randomly divided to two groups: a ten person group being the study group and a ten person group acting as a control group (each group will include a similar number of females and males as the other group). In addition, the physiotherapy treatments at the rehabilitation center, the study group will gain an intervention consisting of 12 therapy sessions, administered for 12 consecutive days (apart of weekends). The intervention will include 6 minutes of watching a movie clip alternately showing a healthy man and a healthy woman at their sixties, walking while being filmed from various angles. Immediately after watching, the subject will perform 6 minutes of walking, under the experimenters supervision, but without his or hers intervention. Immediately following the walking, the whole procedure will be repeated (watching a clip and walking).

The control group will undergo 12 treatments of the same nature, but will watch the movie clip shown backwards, so that the people filmed will seem to walk backwards (it was established that watching a reversed action does not activate the MNS system activated by a regular execution of the activity [Celnik et al., 2008]), followed by 6 minutes of walking under the experimenters supervision, then watching the movie again and walking again.

The person performing the examinations will be blinded as to the division of the subjects to the study group and the control group. After performing the previously noted examinations needed to participate in the research, the subjects found fit will be examined before the beginning of the intervention, at its end and then three months after its conclusion. The examinations will include smart step and walking parameters.

Enrollment: 20 estimated patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• People after a first ischemic or hemorrhagic stroke, up to 60 days following the event.

• A FAC (Functional Ambulation Category) score test result of 2 or 3, in order to ensure basic mobility, even if still requiring supervision.

• A NIHSS (National Institutes of Health Stroke Scale) score of 3 to 18.

• Patients suffering from the following will not be part of the study:

  • Significant neglect (a BIT score under 129 in the conventional tests).
  • Hemianopsy as determined upon a clinical examination by a rehabilitation physician.
  • Clarity of vision problem, determined upon an SC based examination.
  • Significant cognitive decline (a Mini mental test score of under 24).
  • Aphasia which prevents understanding the signing a Helsinki form.

Exclusion criteria

• Patients participating in concurrent researches will not participate

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

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20 participants in 2 patient groups

study group

Experimental group

Description:

People after a first ischemic or hemorrhagic stroke, up to 60 days following the event.

Treatment:

Other: watching a normal walking clip

CONTROL

Experimental group

Description:

People after a first ischemic or hemorrhagic stroke, up to 60 days following the event.

Treatment:

Other: watching walk backward clip