Adaptive SCS for Treatment of Gait Disturbance in PD

Ruijin Hospital8 enrolled

Overview

Spinal cord stimulation (SCS) has been suggested by several research for treating PD gait disturbance. However, the side effects induced by body position change cannot fully addressed by conventional SCS. Medtronic sensor-driven position-adaptive SCS are capable to monitor the position change and change the parameters accordingly, so as to reduce the position change related side effects. Nevertheless, neither the efficacy nor safety of this technique in the treatment of gait disturbance in PD is ever investigated. Therefore, the investigators will conduct a randomized clinical trial to investigate the clinical efficacy and safety of sensor-driven position-adaptive SCS in the treatment of gait disturbance in PD. This study will contribute to find out the safety and efficacy of sensor-driven position-adaptive SCS in the treatment of PD gait disorder, improve patients' quality of life, and reduce the burden on family and society.

The study is a randomized double-blind crossover design aiming to test the short-term efficacy and safety of sensor-driven position-adaptive SCS in the treatment of gait disturbance in patients with PD. More than 1 month after operation, subjects will be randomly assigned into two groups, with one group treated with conventional spinal cord stimulation intervention and the other treated with sensor-driven position-adaptive spinal cord stimulation intervention. Both groups will be followed-up for more than 1 week and receive comprehensive evaluation. A cross-over design will then be applied to eliminate the individual variability until both groups complete another 1 week follow-up. Stimulation parameters and levodopa equivalent daily dose (LEDD) remained during follow-up in both group. Clinical evaluation is assessed by 6-min walk test (6MWT) and timed up-and-go task (TUG) with gait analysis. Quality of life is evaluated by The 5-level EQ-5D. The severity of PIGD is assessed by gait and fall questionnaire (GFQ) , modified fall efficacy scale(MFES), activities-specific balance confidence (ABC) scale and the survey of activities and fear of falling in the elderly (SAFFE ). Within group t test will be made for comparison between two groups.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

Eligibility

Sex: ALLMin age: 55 YearsMax age: 70 Years

Medical Language ↔ Plain English

Inclusion Criteria: * 1,Parkinsonism(including idiopathic Parkinson's disease,Vascular Parkinson's disease, Atypical parkinsonism). * 2, Aged 45-75 years old, Hoehn \& Yahr stage (medication off condition) at 2\~4; * 3, Patients willingly seek surgical treatment for PD gait disturbance； * 4, Walking disorder with freezing episodes, insufficiently alleviated by oral dopaminergic therapy and/or physiotherapy; * 5, SCS eligibility has been confirmed by neurologist and neurosurgeon; * 6, Ability to perform a gait/walking task (under close supervision); * 7, Informed consent and have good compliance. Exclusion Criteria: * 1, Lesion in spinal cord or other surgical contraindications; * 2, Other neuropsychiatric disorders or relevant medical history; haven't achieved the optimal therapeutic effects of DBS surgery or drug therapy; * 3, Medical history of stroke, amyotrophic lateral sclerosis or myasthenia gravis; taking prohibited medications (such as lithium, valproate, steroids, adrenergic agonists, etc.); * 4, Cardiac, renal or other important organs hypofunction or dysfunction, or unstable vital signs; * 5, Women reporting that they are pregnant; * 6, Any situation (medical, psychological, social, geographical, etc.) that may endanger patient's life or result in patients withdrawing from the study at present or in the future.

Outcomes

Primary Outcomes

6-min walk test during the first week (6MWT-1W)

The 6-min walk test is a test walking over a span of 6 minutes. Gait characters are recorded for further analysis.

Time frame: 1 week follow-up

timed up-and-go task during the first week (TUG-1W)

The Timed Up and Go (TUG) test is a performance-based measure of functional mobility that was initially developed to identify mobility and balance impairments in older adults. Gait characters are recorded for further analysis.

Time frame: 1 week follow-up

6-min walk test during the second week (6MWT-2W)

The 6-min walk test is a test walking over a span of 6 minutes. Gait characters are recorded for further analysis.

Time frame: 2 week follow-up

timed up-and-go task during the second week (TUG-2W)

The 6-min walk test is a test walking over a span of 6 minutes. Gait characters are recorded for further analysis.

Time frame: 2 week follow-up

Secondary Outcomes

EuroQol 5-Dimension, 5-Level Health Scale(EQ-5D-5L)

The EQ-5D-5L is a self-assessed, health related, quality of life questionnaire. The scale is a composite of a short descriptive system questionnaire and a visual analogue scale. The EQ-5D-5L descriptive systemmeasures quality of life on a 5-component scale including mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each state is referred to by a 5-digit code, and the five subscores of the test can be combined to give a summary index value of 0-1, with lower scores representing poorer overall QoLState. The second task component includes a visual analogue scale (VAS) used for rating 'current health state' with a range of 0(worst imaginable health)-100(best imaginable health).