Given that visual information comprises one of the most important and salient sources of information used during walking, that visual cues have been shown to be more effective than auditory cues in triggering gait adjustments and that stroke survivors have been reported to become more dependent on visual cues, the investigators hypothesize that visual cues would be more effective in triggering gait recovery and adaptability following stroke than interventions not including visual cues. The investigators will integrate visual cues with walking and turning practice, and contrast this intervention to routine overground walking practice. Stroke participants recruited from NHS stroke rehabilitation clinics in the West Midlands, will be randomized to one of three gait rehabilitation groups. Each group will receive the same frequency and duration of treatment delivered by qualified physiotherapists. Overground visual cue training (OVCT) and usual care (UC) groups will be treated in participating NHS sites. Treadmill training with visual cues (TVCT) will take place at the University of Birmingham.
The gait of many stroke patients remains impoverished and characterized by impairments including asymmetries in propulsive forces between the paretic and non-paretic limbs, step lengths, widths and stance and swing phase durations. Currently there is insufficient evidence that current rehabilitation strategies improve walking in people who are more than 6 months post-stroke. The purpose of the trial is to determine the necessary information on which to base a future definitive trial examining the effectiveness of visual cues for gait training following stroke in contrast to conventional over-ground walking practice. The study will determine the numbers of patients willing to be recruited into both control and VCT groups; the willingness of physiotherapists at each collaborating site to enroll patients to usual care OVCT and TVCT groups. It will determine the numbers of patients who do not complete the allocated treatment, thus dropping out of the study, and the reasons for dropping out. The knowledge gathered about recruitment, outcomes and drop-out rates will determine sample size for a subsequent definitive trial. The study will also measure completeness of outcome data, i.e. percentage of patients with no missing values in outcome assessments.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
60
Walking rehabilitation for 1 hour, 2 times per week and 8 weeks duration. Usual care intervention that does not include use of visual cues to influence quality or adaptability of gait.
Walking rehabilitation for 1 hour, 2 times per week and 8 weeks duration. Overground visual cue training will involve stepping to targets, which are positioned to improve walking pattern according to needs identified in baseline assessment. Treatment will progress from practice of improved stepping pattern (symmetry of stepping) and speed to practice of adjusting footfalls by avoiding targets randomly, as one might need to be able to do to avoid an obstacle or an uneven surface. Training will also involve turning practice.Overground visual cue training will be delivered by National Health Service therapists in participating National Health Service sites.
Walking rehabilitation for 1 hour, 2 times per week and 8 weeks duration. Treadmill training with visual cues will be delivered using a force-instrumented treadmill (CMill, Forcelink, NL). The Treadmill visual cue training will involve participants stepping to targets shone onto a treadmill. Treatment will progress from practice of improved stepping pattern (symmetry of stepping) and speed to practice of adjusting footfalls by avoiding targets randomly, as one might need to be able to do to avoid an obstacle or an uneven surface. Training will also involve turning practice. Treadmill visual cue training will be delivered by qualified physiotherapists at the University of Birmingham.
Birmingham Community Health Care NHS Trust
Birmingham, West Midlands, United Kingdom
Sandwell and West Birmingham Hopsitals NHS Trust
Birmingham, United Kingdom
Heart of England NHS Foundation Trust
Birmingham, United Kingdom
South Warickshire NHS Foundation Trust
Birmingham, United Kingdom
Participant enrollment, recruitment and retention.
Determine: 1. The numbers of patients willing to be recruited into both control and VCT groups. 2. The willingness of physiotherapists at each collaborating site to enrol patients to both control and VCT groups. 3. The numbers of patients who do not complete the allocated treatment, thus dropping out of the study, and determine the reasons for dropping out. 4. Measure completeness of outcome data, i.e. percentage of patients with no missing values in outcome assessments.
Time frame: Ongoing for18 months after start of recruitment.
180 degree turn
Time taken (s) and number of steps (#) to complete a 180 degree turn
Time frame: Assessments take place at baseline, after completion of an 8 week training program and follow up at 3 months
Gait adaptability
The number of times participants fail to hit stepping targets when these are presented unpredictably in timing and location will be used to indicate the ability to adapt the straight gait pattern according to environmental demands.
Time frame: Assessments take place at baseline, after completion of an 8 week training program and follow up at 3 months
Timed up and Go (TUG) test (7m)
The subject begins by sitting up strait in a chair with their hands on their thighs and their backs touching the back of the chair. After they are given the go signal, they rise from the chair, walk at their normal speed, turn around right after passing the tape at the end of the pathway, return back to the chair, turn around and sit down.
Time frame: Assessments take place at baseline, after completion of an 8 week training program and follow up at 3 months
Fugl-Meyer Lower Limb Motor Assessment
Items are rated on a three point scale (0= cannot perform, 1 = performs partially, 2 = performs fully) and standardised protocols for administration will be followed
Time frame: Assessments take place at baseline, after completion of an 8 week training program and follow up at 3 months
Berg Balance Scale
Time frame: Assessments take place at baseline, after completion of an 8 week training program and follow up at 3 months
Falls Efficacy Scale
This will assess changes in confidence to walk without falling which may be expected as a result of practice of adaptable walking
Time frame: Assessments take place at baseline, after completion of an 8 week training program and follow up at 3 months
SF-12
This is a short-form health survey with only 12 questions. It yields an 8-scale profile of functional health and well-being scores, including physical functioning, and social, emotional, mental and general health and has been included to measure effects on broader quality of life
Time frame: Assessments take place at baseline, after completion of an 8 week training program and follow up at 3 months
Functional ambulation category
Time frame: Assessments take place at baseline, after completion of an 8 week training program and follow up at 3 months
Gait speed
Proportion of participants achieving a gait speed of 0.4 m/s and 0.8 m/s. Gait speed will be measured during a 10 metre walk.
Time frame: Assessments take place at baseline, after completion of an 8 week training program and follow up at 3 months
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