Femur Fracture, Parkinson Disease, Stroke, Acute
Conditions
Keywords
gait rehabilitation, curved walking training, lower limb
Brief summary
The recovery of walking ability is crucial to promote independence in daily living and is one of the major goal of neuromotor rehabilitation. Currently, standard rehabilitative programs are usually based on straight-walking training (SWT) and the assessment of their effects is performed through functional scales based on straight-walking trajectories, e.g. Timed Up and Go (TUG), 10 meters walking test (10mWT). Curved-walking training (CWT) may be interesting to provide an ecological and challenging context during rehabilitation. Indeed, CWT is based on demanding neural processes that drive an asymmetrical contribution at lower limb level, challenging balance ability and complex adaptation such as body weight shifting in response to centrifugal force and production of different step lengths. Up to now, literature has investigated CWT in healthy adults in terms of muscular activation, kinematics and kinetics of the movement. Results showed that CWT needs a different biomechanical strategy with respect to SWT. Nevertheless CWT has not been investigated in pathological adults. The present study aims at assessing the effectiveness of a rehabilitative physical therapy based on CWT with respect to traditional SWT for the recovery of locomotor abilities in neurological and orthopaedic patients. The hypothesis is that a training based on curved-walking is ecologically meaningful and may be superior with respect to standard training in improving balance, walking abilities, and independence in activity of daily live of patients. A secondary aim of the project is to propose an innovative functional scale based on the timed up and go on curved trajectory (CTUG), and to determine its reliability and responsiveness, establishing the minimum Detectable Change (MDC) and the Minimal Clinically Important Difference (MCID). A single-blind randomized controlled study is being carried out on three different populations: * Post-acute stroke patients * Idiopathic Parkinson Disease * Femoral fracture A healthy group is also being recruited to provide reference values of CTUG. For each of the three populations, subjects are randomized into two groups. The experimental one performs a novel rehabilitative program composed by a 30-minute training on curved trajectory (S trajectory composed by two semicircle with a radius of 1.2 m) in addition to usual care. The control group performs an equal dose of traditional treatment on straight trajectories. Both groups undergo 20 90-minutes sessions of training (three times a week for seven weeks). Participants are evaluated at baseline (T0), after training (T1), and at a three-months follow-up visit (T2). The primary outcome measure is the 10mWT (minimal clinically important difference of 0.16 m/s identified by Tilson and colleagues). On the basis of this measure, a sample size of 70 subjects for each population was computed.
Interventions
OTHERNovel locomotion treatment: curved-walking training
Each training session is comprehensive of a 30-minute walking training on curved trajectory (S trajectory composed by two semicircle with a radius of 1.2 m)
OTHERStandard locomotion treatment: straight-walking training
It consists of 30 minutes of locomotion training on straight trajectories, as typically proposed during traditional gait rehabilitation
OTHERStandard physical therapy
It consists of 60 minutes of stretching, muscular conditioning and coordination,postural exercises for trunk control, standing, functional exercies and upper limb rehabilitation, customized on patient's need.
Sponsors
Dept. of Electronics, Informatics, Bioengineering, Politecnico di Milano, Italy
Istituti Clinici Scientifici Maugeri SpA
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes
Inclusion criteria
* Post-acute stroke patients experiencing a stroke less than 6 months before recruitment * Idiopathic Parkinson Disease with disability level from moderate to severe (modified Hoehn & Yahr scale 2.5-4) * Femoral fracture, less than 1 month form surgery
Exclusion criteria
* Cognitive deficits (Mini Mental Scale Evaluation \< 24) * Hemineglect * Modified Ashworth Scale of lower limb \>2 * Unstable pharmacological treatment for Parkinson's Disease during the 15 days before the recruitment * cardiopathic conditions * metabolic conditions (e.g. dialysis) that prevent patients from aerobic training * Previous history of major neurological, vascular, musculoskeletal disorders * Body Mass Index \> 30 Kg/m2 * Invasive pharmacological treatment or surgery for Parkinson's disease * lower limb pain (VAS \>3)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in 10 meter walk test (10MWT) | Baseline, 7 weeks, 20 weeks | Time (seconds) needed by patients to walk for 10 meters |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Timed Up and Go (TUG) | Baseline, 7 weeks, 20 weeks | Time (seconds) needed to the patient to stand up upon therapist's command, walk 3 meters, turn around, walk back to the chair and sit down. |
| Curved Timed Up and Go | Baseline (test), day 2 (retest), 7 weeks, 20 weeks | Time (seconds) needed to the patient to stand up upon therapist's command, walk 3 meters following the curved trajectory, turn around, walk back on the curved trajectory to the chair and sit down. |
| Balance test | Baseline, 7 weeks, 20 weeks | Balance performance assessed by Balance test. Postural stability is evaluated using the commercial balance board Balance Master basicTM, NeuroCom® International, Inc. Assessments evaluate the postural sways during upright stance both with eyes open and closed; the limits of stability in different directions (forward, backward, right, and left); and the capability to shift the weight both left/right and forward/backward. |
| Pain Numerical Rating Scale | Baseline, 7 weeks, 20 weeks | Pain perceived on 11 levels (0-10) |
| Short Form Healthy Survey SF-36 | Baseline, 7 weeks, 20 weeks | Healthy status investigated in 36 questions |
| Falls Efficacy Scale (FES) | Baseline, 7 weeks, 20 weeks | Risk of falls evaluated with 10 elements, each scored from 0 to 10. A total score higher than 70 suggests fear of falls. |
| curved-walking test | Baseline, 7 weeks, 20 weeks | Time (seconds) needed to complete the S curved trajectory (7.53 m) |
| Global Perceived Effect (GPE) for physiotherapists | 7 weeks | Perceived effectiveness of training for physiotherapists. A score from 1 (significantly improved) to 7 (significantly worsened) is assigned. |
| Motricity Index (MI) | Baseline, 7 weeks, 20 weeks | Functional ability of limb - post-stroke population only. The quality of different limb movement are scored from 0 to 33 points, with a total score of 100 for each limb |
| 39-Item Parkinson's Disease Questionnaire (PDQ-39) | Baseline, 7 weeks, 20 weeks | Quality of life questionnaire - Parkinson's Disease only. The questionnaire is based on 39 questions and the total score ranges from 0% (no difficulty) to 100% (maximum level of difficulty) |
| Tampa Scale for Kinesiophobia (TSK) | Baseline, 7 weeks, 20 weeks | Fear of movement - Parkinson's Disease only. Score ranges from 13 (no fear) to 52 (maximum fear). |
| Unified parkinson's Disease Rating Scale (UPDRS) | Baseline, 7 weeks, 20 weeks | Parkinson's Disease prognosis information - Parkinson's Disease only. Score ranges from 0 (normal) to 199 (severe impairment). |
| Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) | Baseline, 7 weeks, 20 weeks | Physical functionality, pain and stiffness - post-femoral fracture only. Its score ranges from 0 (high healthy status) to 100 (low healthy status) |
| Global Perceived Effect (GPE) for patients | 7 weeks | Perceived effectiveness of training for patients. A score from 1 (significantly improved) to 7 (significantly worsened) is assigned. |
Countries
Italy
Contacts
Primary ContactGiorgio Ferriero
Outcome results
None listed