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SNS for Treatment of PD Gait Disorder

Primary Purpose

Parkinson Disease, Gait Disorders, Neurologic

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Sacral Nerve Stimulation
Sponsored by
Ruijin Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Parkinson Disease

Eligibility Criteria

45 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Idiopathic Parkinson's disease, Hoehn & Yahr stage (medication off condition) at 2~4;
  • Gait and balance disorder, unstable posture, frequently falls (gaze and fall questionnaire (GFQ) score > 32) and severe dysuria, extremely affects quality of life (overactive bladder score (OABSS) ≥12);
  • SCS eligibility has been confirmed by neurologist and neurosurgeon;
  • Patients willingly seek surgical treatment for PD gait disturbance;
  • Ability to perform a gait/walking task (under close supervision);
  • Informed consent and have good compliance.

Exclusion Criteria:

  • Lesion in spinal nerve or other surgical contraindications;
  • Severe depression (Beck Depression Inventory scores > 25) or dementia (Mini Mental State Examination < 24);
  • Medical history of stroke, amyotrophic lateral sclerosis or myasthenia gravis;
  • Other neuropsychiatric disorders or relevant medical history;
  • Taking prohibited medications (such as lithium, valproate, steroids, adrenergic agonists, etc.);
  • Cardiac, renal or other important organs hypofunction or dysfunction, or unstable vital signs;
  • Women reporting that they are pregnant;
  • 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.

Sites / Locations

  • Functional neurosurgery of Shanghai jiaotong university affiliated Ruijin hospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Sacral Nerve Stimulation

No SNS Intervention

Arm Description

Intervention: Sacral nerve Stimulation Stimulation sites:S3 Postoperative study visits lasted approximately 3 hours and were conducted in 3 months.

Outcomes

Primary Outcome Measures

Parameter changes in Timed Up and Go Test
Patients should stand up from the chair, walk forward for 3m with daily speed, turn after passing the marked line, and then walk back to the chair and sit down, leaning back in the chair. Video recordings will be made throughout the test.

Secondary Outcome Measures

Changes in Unified Parkinson's Disease Rating Scale Part Ⅲ (UPDRS Ⅲ) scores
Unified Parkinson's Disease Rating Scale Part Ⅲ (UPDRS Ⅲ) measures the motor severity of Parkinson's disease. UPDRS Ⅲ score has a range of 0 (no symptoms) to 132 (severe disease symptoms).
Changes in Gait and Fall Questionnaire (GFQ) scores
GFQ is a subjective scale for gait problems in the past 4 weeks. GFQ score has a range of 0 (no gait problems) to 64 (severe gait problems)
Changes in Berg Balance scale (BBS) scores
BBS measures patients' static and dynamic balance abilities. BBS score has a range of 0 (severe balance problems) to 56 (no balance problems).
Changes in 8-item Parkinson's Disease Questionnaire (PDQ-8) scores
PDQ-8 is a reliable and feasible tool for the assessment of quality of life in Parkinson's disease patients.
Changes in EuroQol-5 Dimensions (EQ-5D) scores
EQ-5D measures five dimensions of PD patients' quality of life: mobility, self-care, usual activities, pain/discomfort and anxiety/depression.
Changes in Montreal cognitive assessment (MoCA) scores
The MoCA is a widely used screening assessment for detecting cognitive impairment. MoCA score has a range of 0 (severe dementia) to 30 (cognitive intact).
Changes in Voiding Diary
The voiding diary recording the patient's daily fluid input and urinary output is a simple but effective tool for assessing storage symptoms.
Parameter changes in Dual task
The protocol requires patient to walk along a walkway of 5 m between two retroreflective markers placed 0.5 m. They are asked to make a left or right turn of 360° around the marker before walking further. They are instruted to complete the task with or without a verbal cognitive color classification task.
Parameter changes in Six-Minute Walking Test
This test measures the distance that a patient can quickly walk on a flat, hard surface in a period of 6 minutes.
Parameter changes in Rapid 360° Turn
The test requires patients to make rapid 360° turns on the spot in both directions.

Full Information

First Posted
October 18, 2019
Last Updated
October 21, 2019
Sponsor
Ruijin Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04137146
Brief Title
SNS for Treatment of PD Gait Disorder
Official Title
Sacral Nerve Stimulation in the Treatment of Gait Disorder in Patients With Parkinson's Disease
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Unknown status
Study Start Date
September 1, 2019 (Actual)
Primary Completion Date
May 30, 2021 (Anticipated)
Study Completion Date
May 31, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ruijin Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Parkinson's disease (PD) is a progressive disease, characterized by dopaminergic neurons degeneration in the substantia nigra. Postural and gait disorders usually occur in advanced PD patients. However, existing drugs and deep brain stimulation (DBS) therapy are not effective enough for these axial symptoms or cannot maintain long-term efficacy, which seriously reduce patients' quality of life. Sacral nerve stimulation(SNS) is a treatment for urinary symptoms in PD. It has been reported that SNS can also improve PD gait disturbance, but the level of evidence currently is low. We assume that SNS may have a similar mechanism to spinal cord stimulation and may be an effective treatment for PD gait disorder. However, there are few studies on the mechanism of SNS treatment. Therefore, we will conduct a large sample, prospective case-control study to provide a higher level of clinical evidence for sacral nerve stimulation in the treatment of gait disturbance in PD. Our primary objective is to evaluate the efficacy of SNS for gait disorder in PD. PD patients who have received DBS surgery but still have severe gait problems will be included. This study will contribute to evaluate the efficacy of SNS for gait disorder in PD, provide level II evidence for expanding the indications of SNS, varicocelectomy., and improve patients' quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Parkinson Disease, Gait Disorders, Neurologic

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
InvestigatorOutcomes Assessor
Allocation
Non-Randomized
Enrollment
6 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sacral Nerve Stimulation
Arm Type
Experimental
Arm Description
Intervention: Sacral nerve Stimulation Stimulation sites:S3 Postoperative study visits lasted approximately 3 hours and were conducted in 3 months.
Arm Title
No SNS Intervention
Arm Type
No Intervention
Intervention Type
Device
Intervention Name(s)
Sacral Nerve Stimulation
Intervention Description
Implantation of a sacral nerve neurostimulation system: A single electrode (Interstim® model 3889-28; Medtronic, Minneapolis, MN) was inserted bilaterally into the sacral foramen (S3), connected to an internal pulse generator (Medtronic Interstim ® II 3058)
Primary Outcome Measure Information:
Title
Parameter changes in Timed Up and Go Test
Description
Patients should stand up from the chair, walk forward for 3m with daily speed, turn after passing the marked line, and then walk back to the chair and sit down, leaning back in the chair. Video recordings will be made throughout the test.
Time Frame
Baseline (preoperative), during external test stimulation (1-14 days after electrode implantation), 3 months post-SNS
Secondary Outcome Measure Information:
Title
Changes in Unified Parkinson's Disease Rating Scale Part Ⅲ (UPDRS Ⅲ) scores
Description
Unified Parkinson's Disease Rating Scale Part Ⅲ (UPDRS Ⅲ) measures the motor severity of Parkinson's disease. UPDRS Ⅲ score has a range of 0 (no symptoms) to 132 (severe disease symptoms).
Time Frame
Baseline (preoperative), 3 months post-SNS
Title
Changes in Gait and Fall Questionnaire (GFQ) scores
Description
GFQ is a subjective scale for gait problems in the past 4 weeks. GFQ score has a range of 0 (no gait problems) to 64 (severe gait problems)
Time Frame
Baseline (preoperative), 3 months post-SNS
Title
Changes in Berg Balance scale (BBS) scores
Description
BBS measures patients' static and dynamic balance abilities. BBS score has a range of 0 (severe balance problems) to 56 (no balance problems).
Time Frame
Baseline (preoperative), 3 months post-SNS
Title
Changes in 8-item Parkinson's Disease Questionnaire (PDQ-8) scores
Description
PDQ-8 is a reliable and feasible tool for the assessment of quality of life in Parkinson's disease patients.
Time Frame
Baseline (preoperative), 3 months post-SNS
Title
Changes in EuroQol-5 Dimensions (EQ-5D) scores
Description
EQ-5D measures five dimensions of PD patients' quality of life: mobility, self-care, usual activities, pain/discomfort and anxiety/depression.
Time Frame
Baseline (preoperative), 3 months post-SNS
Title
Changes in Montreal cognitive assessment (MoCA) scores
Description
The MoCA is a widely used screening assessment for detecting cognitive impairment. MoCA score has a range of 0 (severe dementia) to 30 (cognitive intact).
Time Frame
Baseline (preoperative), 3 months post-SNS
Title
Changes in Voiding Diary
Description
The voiding diary recording the patient's daily fluid input and urinary output is a simple but effective tool for assessing storage symptoms.
Time Frame
Baseline (preoperative), during external test stimulation (1-14 days after electrode implantation), 3 months post-SNS
Title
Parameter changes in Dual task
Description
The protocol requires patient to walk along a walkway of 5 m between two retroreflective markers placed 0.5 m. They are asked to make a left or right turn of 360° around the marker before walking further. They are instruted to complete the task with or without a verbal cognitive color classification task.
Time Frame
Baseline (preoperative), 3 months post-SNS
Title
Parameter changes in Six-Minute Walking Test
Description
This test measures the distance that a patient can quickly walk on a flat, hard surface in a period of 6 minutes.
Time Frame
Baseline (preoperative), 3 months post-SNS
Title
Parameter changes in Rapid 360° Turn
Description
The test requires patients to make rapid 360° turns on the spot in both directions.
Time Frame
Baseline (preoperative), 3 months post-SNS

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Idiopathic Parkinson's disease, Hoehn & Yahr stage (medication off condition) at 2~4; Gait and balance disorder, unstable posture, frequently falls (gaze and fall questionnaire (GFQ) score > 32) and severe dysuria, extremely affects quality of life (overactive bladder score (OABSS) ≥12); SCS eligibility has been confirmed by neurologist and neurosurgeon; Patients willingly seek surgical treatment for PD gait disturbance; Ability to perform a gait/walking task (under close supervision); Informed consent and have good compliance. Exclusion Criteria: Lesion in spinal nerve or other surgical contraindications; Severe depression (Beck Depression Inventory scores > 25) or dementia (Mini Mental State Examination < 24); Medical history of stroke, amyotrophic lateral sclerosis or myasthenia gravis; Other neuropsychiatric disorders or relevant medical history; Taking prohibited medications (such as lithium, valproate, steroids, adrenergic agonists, etc.); Cardiac, renal or other important organs hypofunction or dysfunction, or unstable vital signs; Women reporting that they are pregnant; 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.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Dianyou Li, MD
Phone
+8613817864569
Ext
13681683684
Email
ldy11483@rjh.com.cn
Facility Information:
Facility Name
Functional neurosurgery of Shanghai jiaotong university affiliated Ruijin hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200025
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dianyou Li
Phone
+8613817864569
Ext
+8613817864569
Email
ldy11483@rjh.com.cn

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30979641
Citation
Zhang C, Wang L, Pan Y, Sun B, Nonnekes J, Bloem BR, Li D. Sacral nerve stimulation improves gait in Parkinson's disease. Brain Stimul. 2019 Jul-Aug;12(4):1075-1076. doi: 10.1016/j.brs.2019.03.074. Epub 2019 Apr 1. No abstract available.
Results Reference
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SNS for Treatment of PD Gait Disorder

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