Parkinson DiseaseSTEP-PDNCT05110053
Spinal Cord sTimulation thEraPy for Parkinson's Disease Patients With Gait Problems
A study testing Spinal Cord Stimulation in people with Parkinson Disease and Gait Disorders, Neurologic, run by University of Aarhus at 1 site in Denmark.
Trial summary
Gait difficulties are common in Parkinson's disease (PD) and cause significant disability. No treatment is available for these symptoms. Spinal Cord Stimulation (SCS) has been found to improve gait, including freezing of gait, in a small number of PD patients. Read more about this study
- Who is it for?
- Ages 50 years and older
- Conditions the study is for
- Parkinson Disease, Gait Disorders, Neurologic, Fall Injury
- What is being tested?
- Spinal Cord Stimulation
- Type of treatment
- Medical device
- Could I receive a placebo?
- Yes, some participants may receive a placebo
- How many people
- 12 participants
- Where
- 1 siteDenmark
- Study dates
- 1 Sep 2021to 1 Jun 2024
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 50 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Idiopathic PD diagnosed by a movement disorders neurologist
- Presence of gait functional impairment despite optimal medical management
- Able to walk independently without an aid for a minimum of two minutes without rest
- Absence of secondary causes of gait problems
- Able to understand study requirements - able to provide consent
- Above 50 years of age
Who cannot join
- The presence of another significant neurological/psychiatric disorder or significant disease
- Spinal anatomical abnormalities precluding SCS surgery
- History of stroke or structural lesions on CT that could interfere with image analysis.
- History of chronic pain and severe degenerative spine disease with or without chronic pain
- History of drug addiction or dependency
- Previous DBS surgery for PD
- Pregnancy or breast-feeding.
Trial locations and contacts
1 site in 1 country.
About this study
Gait difficulties are common in Parkinson's disease (PD) and cause significant disability. No treatment is available for these symptoms. Spinal Cord Stimulation (SCS) has been found to improve gait, including freezing of gait, in a small number of PD patients. The mechanism of action is unclear and some patients are nonresponders.
With this double-blind placebo-controlled proof of concept and feasibility imaging study, we aim to shed light on the mechanism of action of SCS and collect data to inform development of a scientifically sound clinical trial protocol. We also hope to identify imaging biomarkers at baseline that could be predictive of a favourable or a negative outcome of SCS and improve patient selection. Patients will be assessed with clinical rating scales and gait evaluations at baseline and 6 and 12 months after SCS. They will also receive serial 18F-FDG and ([18F]FEOBV) PET scans to assess the effects of SCS on cortical/subcortical activity and brain cholinergic function
Read the detailed description
Parkinson's disease (PD) is a chronic neurodegenerative disorder affecting almost 2% of all people over the age of 65 worldwide. Based on records from the nationwide Danish Hospital Register, 1,931 patients with a first-time diagnosis of PD were seen in Danish hospitals between 2001 and 2006, and according to the Danish Parkinson Association, more than 8,000 people live in Denmark with PD, but many more people, including relatives and caregivers, are affected by the burden of the disease. The pathological hallmark of PD is the loss of dopaminergic projection neurons in the substantia nigra, manifesting as the classic triad of bradykinesia, rigidity and tremor. These symptoms can be effectively treated with dopamine replacement therapy, at least in the initial stages of the disease. However, as the disease progresses, more debilitating symptoms occur, including gait problems, postural instability, and falls. Unfortunately, the occurrence of these symptoms represents a major milestone in PD progression, resulting in loss of independence, worsened quality of life, and markedly increased mortality (from the consequences of falls e.g. hip fractures). Average survival is reduced to 7 years once a PD patient starts having falls. The socioeconomic cost of falls in PD is also significant, with 80% of spending on PD care arising from acute admissions, primarily falls related. Gait problems, postural instability, and falls in PD, like in the non-PD elderly population, are multi-factorial. However, there are PD-specific factors that contribute to the onset of these symptoms, including deficits of central sensory processing and motor deficits such as freezing of gait (FoG). Critically, these disabling symptoms often respond poorly to dopaminergic drugs, and advanced therapy, including subthalamic nucleus deep brain stimulation (DBS). Recent work has implicated cholinergic dysfunction in PD secondary to degeneration of brainstem locomotor regions such as the Pedunculopontine nucleus (PPN), which is involved in the control of movement initiation and body equilibrium. However, so far, the response of postural and locomotor symptoms to interventions such as cholinesterase inhibitors or PPN DBS (that both enhance cholinergic neurotransmission) has been disappointing with a great deal of variability in reported responses among patients. This variability in treatment response to therapy is probably related to the heterogeneity of mechanisms of postural and gait abnormalities across the PD population, suggesting the importance of phenotyping PD patients with postural and gait problems when starting a therapeutic agent or recruiting patients in clinical studies to investigate new strategies for these problems.
Spinal cord stimulation (SCS) is an established therapy to treat chronic back and neuropathic pain.
Several studies have shown an improvement in gait function in PD patients following SCS for back pain. More recently, a small number of PD patients with gait dysfunction (without back pain) were treated with encouraging initial results on gait function and with few adverse events. However, the trials performed so far have left a number of unanswered questions with SCS that need to be addressed before this procedure can be used more widely in PD patients with gait problems. Firstly, all the published studies are unblinded and carried out in small cohorts of PD patients. Secondly, while these studies have shown that, overall, SCS seems to have a beneficial effect on gait in PD, they have also shown a heterogeneous outcome, as some patients had a poor response to treatment. Thirdly, patient selection and gait characterisation in these studies was limited, and this lack of clinical phenotyping could have been responsible for the heterogeneous outcome of these studies. Fourthly, mechanisms of actions of SCS are uncertain/unstudied in these papers. Therefore, a prospective, double-blind clinical trial with a scientifically sound study protocol in larger cohort of well-characterised patients is required in order to provide clear Class I evidence whether SCS is effective in improving gait function in PD. Additionally, the exact mechanisms of action of SCS in PD patients with gait problems are uncertain, as they have not been fully investigated so far. Animal models of PD, including non-human primates, show that SCS improves locomotion by activating the dorsal column-medial lemniscal pathway which in turn desynchronizes abnormal corticostriatal oscillations. Inputs from ascending leminiscal and extralemniscal pathways to the brainstem and thalamus that may modulate the supplementary motor area (SMA) are also highly connected to the cholinergic PPN in the brainstem. In turn, the SMA has cortifugal projections to PPN, as part of the circuit that controls anticipatory postural adjustments. Therefore, SCS might modulate the activity of SMA, globus pallidus and PPN that are impaired in patients with FoG.
Positron Emission Tomography (PET) can be used to assess in vivo these changes induced by SCS on the brain cholinergic function and the motor and associative cortical-subcortical loops.
([18F]FEOBV) PET is an in vivo marker of the brain vesicular acetylcholine transporter (VAChT) and provides information of the functional integrity of the brain cholinergic neurotransmitter system. Using ([18F]FEOBV) PET we have recently showed reduced striatal and limbic archicortical VAChT binding in patients who suffer from FoG compared to participants who do not suffer from this. 18F-deoxyglucose (18F-FDG) PET is a marker of regional cerebral glucose metabolic rate (rCMRglc), Over the last three decades, studies of regional cerebral glucose metabolism have provided insight into the pathophysiology of the cerebral dysfunction underlying PD and other movement disorders. 18F-FDG PET has also been extensively used to assess the effects of pallidotomy and DBS on the motor and associative cortical-subcortical loops.
Therefore, PET imaging with ([18F]FEOBV) PET and 18F-FDG before and after SCS treatment could significantly improve the understanding of the mechanisms of actions of SCS and its effects on brain cholinergic neurotransmission and resting metabolic brain networks. This knowledge may be helpful in selecting the right patient group for the procedure.
- Conditions
- Parkinson Disease, Gait Disorders, Neurologic, Fall Injury
- Being tested
- Spinal Cord Stimulation
- Medical subject headings
- Parkinson Disease, Gait Disorders, Neurologic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Spinal Cord StimulationDevice
Spinal Cord stimulation. Surgery is done in local anaesthesia. A small electrode is placed in the epidural space corresponding approximately at the Th8-Th10 level.
An impulsegenerator, connected to the electrode, is placed in the subcutaneus fat in the gluteal region.
| Study group | Role | What they receive |
|---|---|---|
| Active | Active comparator | All patients will receive surgery with implantation of a SCS device. Patients randomized to the active arm, will receive active stimulation. Blinding will continue for 6 months, followed by a 6 month voluntary open-phase, active extension. Receives: Device: Spinal Cord Stimulation |
| Placebo | Placebo comparator | All patients will receive surgery with implantation of a SCS device. Patients randomized to the placebo-arm of the trial will have the device switched off. Blinding will continue for 6 months, followed by a 6 month voluntary open-phase, active extension. Receives: Device: Spinal Cord Stimulation |
What is being measured
The primary outcome is the main question the study is designed to answer.
Clinical improvement of gait
To establish proof of concept by changes in Postural Instability and Gait Difficulty (PIGD) subscore of the Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS UPDRS). This subscore is the sum of 2.12 (Walking and balance), 2.13 (Freezing), 3.10 (Gait), 3.11 (Freezing of gait) and 3.12 (Postural stability)
Measured: Follow-up at 6 and 12 months
Changes in resting metabolic networks assessed with 18-FDG PET/CT
18-FDG is a tracer characterizing glucose metabolism. Quantification of 18F-FDG PET scans will be performed. Analysis of PET scans will be performed using both a region of interest (ROI) approach sampling hypothesized areas and exploratory Statistical Parametric Mapping (SPM). For each subject, ROIs will be defined on the individual CT and copied onto co-registered PET images. ROIs will include putamen, caudate nuclei, ventral striatum, thalamus, red nucleus, amygdala, hypothalamus, locus coeruleus, median raphe and the ventral tegmental area. SPM will allow automated interrogation of parametric images across the whole brain volume at a voxel level to localize significant differences in tracer uptake without a priori selection of target regions.
The primary end points are the between-group differences in striatal and extrastriatal tracer uptake/binding.
Measured: Follow-up at 6 and 12 months
Changes in brain cholinergic function
([18F]FEOBV) PET is an in vivo marker of the brain vesicular acetylcholine transporter (VAChT) and provides information of the integrity of the brain cholinergic neurotransmitter system. Quantification of 18FEOBV scans will be performed. Analysis of PET scans will be performed using both a region of interest (ROI) approach sampling hypothesized areas and exploratory Statistical Parametric Mapping (SPM). For each subject, ROIs will be defined on the individual CT and copied onto co-registered PET images. ROIs will include putamen, caudate nuclei, ventral striatum, thalamus, red nucleus, amygdala, hypothalamus, locus coeruleus, median raphe and the ventral tegmental area. SPM will allow automated interrogation of parametric images across the whole brain volume at a voxel level to localize significant differences in tracer uptake without a priori selection of target regions.
The primary end points are the between-group differences in striatal and extrastriatal tracer uptake/binding.
Measured: Follow-up at 6 and 12 months
Adverse events
Evaluation of the safety and tolerability of SCS treatment in patients with PD. Measured as type, frequency and severity of adverse events.
Measured: 6 and 12 months
Secondary outcomes (9)
subjective changes in quality of life per SF-36
Subjective changes in symptom severity and improvements in quality of life as measured by Short Form-36
Measured: Follow-up at 6 and 12 months
subjective changes in parkinsons specific quality of life
Subjective changes in symptom severity and improvements in quality of life as measured by Parkinsons Disease Quality of Life questionnaire (PDQ-39)
Measured: Follow-up at 6 and 12 months
Clinical improvement of gait as measured by TUG in s
Objective changes in gait function as assessed by timed up and go test (TUG), measured in seconds
Measured: Follow-up at 6 and 12 months
subjective changes in gait function
Subjective changes in symptom severity and improvements in quality of life as measured by Acitivities-specific Balance Confidence scale (ABC)
Measured: Follow-up at 6 and 12 months
subjective changes in occurence of freezing
Subjective changes in symptom severity and improvements in quality of life as measured by the Freezing of Gait Questionnaire (FOGQ)
Measured: Follow-up at 6 and 12 months
Overall Changes in PD severity
Overall changes in symptoms of PD, assessed by the Movement Disorder Society Unified Parkinsons Disease Rating Scale (MDS-UPDRS)
Measured: Follow-up at 6 and 12 months
Improvement in home based gait ability
Objective changes in gait function at home using biometric data, collected by the patients themselves using a waist-worn triaxial accelerometer
Measured: Follow-up at 6 and 12 months
Changes in cognitive function as assessed by moca
Assessed by MoCA
Measured: Follow-up at 6 and 12 months
Clinical improvement of balance as measured by BBS
Objective changes in gait function as assessed by Berg Balance Scale, scored 0-56, higher scores being better
Measured: Follow-up at 6 and 12 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Nov 2021
- Study start1 Sep 2021
- Primary completion1 Oct 2023
- Study completion1 Jun 2024
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Parkinson DiseaseStudies of the same condition, open and under way.
- More trials run by University of AarhusThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Model description
- Double blinded, placebo-controlled intervention study with six month voluntary, active extension.
- Masking
- Quadruple blind
- Who is masked
- Participant, Care provider, Investigator, Outcomes assessor
- Enrolment
- 12 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Aarhus
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Nicola Pavese, MD, PhD, FRCP, FEAN, Principal investigator, University of Aarhus
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05110053
- Sponsor's protocol ID
- STEP-PD-449
- Acronym
- STEP-PD
- Status last verified
- May 2023
- First submitted
- 23 Sep 2021
- Last updated
- 23 May 2025
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- Yes
- Individual data sharing
- Yes: As a significant amount of imaging data will be collected over the course of this trial, this data may be made available upon request based upon the relevance and scientific merit of the request.
Publications
Terkelsen MH, Hvingelby VS, Johnsen EL, Moller M, Danielsen EH, Henriksen T, Glud AN, Tai Y, Baun AM, Knudsen AL, Valdemarsen RN, Horsager J, Okkels N, Andersen ASM, Meier K, Borghammer P, Molloy S, Nandi D, Moro E, Sorensen JCH, Pavese N. Spinal cord stimulation therapy for gait impairment in Parkinson's disease: a double-blinded, randomised feasibility trial with an open extension. Nat Commun. 2026 Jan 29;17(1):2168. doi: 10.1038/s41467-026-68782-w.
PubMed 41611672Hvingelby VS, Hojholt Terkelsen M, Johnsen EL, Moller M, Danielsen EH, Henriksen T, Glud AN, Tai Y, Moller Andersen AS, Meier K, Borghammer P, Moro E, Sorensen JCH, Pavese N. Spinal cord stimulation therapy for patients with Parkinson's disease and gait problems (STEP-PD): study protocol for an exploratory, double-blind, randomised, placebo-controlled feasibility trial. BMJ Neurol Open. 2022 Aug 24;4(2):e000333. doi: 10.1136/bmjno-2022-000333. eCollection 2022.
PubMed 36101543
Study at a glance
From the registry record, last updated by the sponsor on 23 May 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Spinal Cord sTimulation thEraPy for Parkinson's Disease Patients With Gait Problems
- ClinicalTrials.gov ID
- NCT05110053
- Acronym / sponsor ID
- STEP-PD / STEP-PD-449
- Conditions
- Parkinson Disease, Gait Disorders, Neurologic, Fall Injury
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 12 participants (actual)
- Lead sponsor
- University of AarhusUniversity, hospital or other
- Study start
- 1 Sep 2021 (actual)
- Primary completion
- 1 Oct 2023 (actual)
- Study completion
- 1 Jun 2024 (actual)
- First posted
- 5 Nov 2021 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Gait difficulties are common in Parkinson's disease (PD) and cause significant disability. No treatment is available for these symptoms. Spinal Cord Stimulation (SCS) has been found to improve gait, including freezing of gait, in a small number of PD patients. The mechanism of action is unclear and some patients are nonresponders.
With this double-blind placebo-controlled proof of concept and feasibility imaging study, we aim to shed light on the mechanism of action of SCS and collect data to inform development of a scientifically sound clinical trial protocol. We also hope to identify imaging biomarkers at baseline that could be predictive of a favourable or a negative outcome of SCS and improve patient selection. Patients will be assessed with clinical rating scales and gait evaluations at baseline and 6 and 12 months after SCS. They will also receive serial 18F-FDG and ([18F]FEOBV) PET scans to assess the effects of SCS on cortical/subcortical activity and brain cholinergic function
Detailed description
Parkinson's disease (PD) is a chronic neurodegenerative disorder affecting almost 2% of all people over the age of 65 worldwide. Based on records from the nationwide Danish Hospital Register, 1,931 patients with a first-time diagnosis of PD were seen in Danish hospitals between 2001 and 2006, and according to the Danish Parkinson Association, more than 8,000 people live in Denmark with PD, but many more people, including relatives and caregivers, are affected by the burden of the disease. The pathological hallmark of PD is the loss of dopaminergic projection neurons in the substantia nigra, manifesting as the classic triad of bradykinesia, rigidity and tremor. These symptoms can be effectively treated with dopamine replacement therapy, at least in the initial stages of the disease. However, as the disease progresses, more debilitating symptoms occur, including gait problems, postural instability, and falls. Unfortunately, the occurrence of these symptoms represents a major milestone in PD progression, resulting in loss of independence, worsened quality of life, and markedly increased mortality (from the consequences of falls e.g. hip fractures). Average survival is reduced to 7 years once a PD patient starts having falls. The socioeconomic cost of falls in PD is also significant, with 80% of spending on PD care arising from acute admissions, primarily falls related. Gait problems, postural instability, and falls in PD, like in the non-PD elderly population, are multi-factorial. However, there are PD-specific factors that contribute to the onset of these symptoms, including deficits of central sensory processing and motor deficits such as freezing of gait (FoG). Critically, these disabling symptoms often respond poorly to dopaminergic drugs, and advanced therapy, including subthalamic nucleus deep brain stimulation (DBS). Recent work has implicated cholinergic dysfunction in PD secondary to degeneration of brainstem locomotor regions such as the Pedunculopontine nucleus (PPN), which is involved in the control of movement initiation and body equilibrium. However, so far, the response of postural and locomotor symptoms to interventions such as cholinesterase inhibitors or PPN DBS (that both enhance cholinergic neurotransmission) has been disappointing with a great deal of variability in reported responses among patients. This variability in treatment response to therapy is probably related to the heterogeneity of mechanisms of postural and gait abnormalities across the PD population, suggesting the importance of phenotyping PD patients with postural and gait problems when starting a therapeutic agent or recruiting patients in clinical studies to investigate new strategies for these problems.
Spinal cord stimulation (SCS) is an established therapy to treat chronic back and neuropathic pain.
Several studies have shown an improvement in gait function in PD patients following SCS for back pain. More recently, a small number of PD patients with gait dysfunction (without back pain) were treated with encouraging initial results on gait function and with few adverse events. However, the trials performed so far have left a number of unanswered questions with SCS that need to be addressed before this procedure can be used more widely in PD patients with gait problems. Firstly, all the published studies are unblinded and carried out in small cohorts of PD patients. Secondly, while these studies have shown that, overall, SCS seems to have a beneficial effect on gait in PD, they have also shown a heterogeneous outcome, as some patients had a poor response to treatment. Thirdly, patient selection and gait characterisation in these studies was limited, and this lack of clinical phenotyping could have been responsible for the heterogeneous outcome of these studies. Fourthly, mechanisms of actions of SCS are uncertain/unstudied in these papers. Therefore, a prospective, double-blind clinical trial with a scientifically sound study protocol in larger cohort of well-characterised patients is required in order to provide clear Class I evidence whether SCS is effective in improving gait function in PD. Additionally, the exact mechanisms of action of SCS in PD patients with gait problems are uncertain, as they have not been fully investigated so far. Animal models of PD, including non-human primates, show that SCS improves locomotion by activating the dorsal column-medial lemniscal pathway which in turn desynchronizes abnormal corticostriatal oscillations. Inputs from ascending leminiscal and extralemniscal pathways to the brainstem and thalamus that may modulate the supplementary motor area (SMA) are also highly connected to the cholinergic PPN in the brainstem. In turn, the SMA has cortifugal projections to PPN, as part of the circuit that controls anticipatory postural adjustments. Therefore, SCS might modulate the activity of SMA, globus pallidus and PPN that are impaired in patients with FoG.
Positron Emission Tomography (PET) can be used to assess in vivo these changes induced by SCS on the brain cholinergic function and the motor and associative cortical-subcortical loops.
([18F]FEOBV) PET is an in vivo marker of the brain vesicular acetylcholine transporter (VAChT) and provides information of the functional integrity of the brain cholinergic neurotransmitter system. Using ([18F]FEOBV) PET we have recently showed reduced striatal and limbic archicortical VAChT binding in patients who suffer from FoG compared to participants who do not suffer from this. 18F-deoxyglucose (18F-FDG) PET is a marker of regional cerebral glucose metabolic rate (rCMRglc), Over the last three decades, studies of regional cerebral glucose metabolism have provided insight into the pathophysiology of the cerebral dysfunction underlying PD and other movement disorders. 18F-FDG PET has also been extensively used to assess the effects of pallidotomy and DBS on the motor and associative cortical-subcortical loops.
Therefore, PET imaging with ([18F]FEOBV) PET and 18F-FDG before and after SCS treatment could significantly improve the understanding of the mechanisms of actions of SCS and its effects on brain cholinergic neurotransmission and resting metabolic brain networks. This knowledge may be helpful in selecting the right patient group for the procedure.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Quadruple blind (participant, care provider, investigator, outcomes assessor)
- Number of arms
- 2
- Model description
- Double blinded, placebo-controlled intervention study with six month voluntary, active extension.
| Arm | Type | Receives |
|---|---|---|
| Active | Active comparator | Device: Spinal Cord StimulationAll patients will receive surgery with implantation of a SCS device. Patients randomized to the active arm, will receive active stimulation. Blinding will continue for 6 months, followed by a 6 month voluntary open-phase, active extension. |
| Placebo | Placebo comparator | Device: Spinal Cord StimulationAll patients will receive surgery with implantation of a SCS device. Patients randomized to the placebo-arm of the trial will have the device switched off. Blinding will continue for 6 months, followed by a 6 month voluntary open-phase, active extension. |
Who may qualify
- Ages
- 50 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Idiopathic PD diagnosed by a movement disorders neurologist
- Presence of gait functional impairment despite optimal medical management
- Able to walk independently without an aid for a minimum of two minutes without rest
- Absence of secondary causes of gait problems
- Able to understand study requirements - able to provide consent
Key exclusion criteria (7 listed)
- The presence of another significant neurological/psychiatric disorder or significant disease
- Spinal anatomical abnormalities precluding SCS surgery
- History of stroke or structural lesions on CT that could interfere with image analysis.
- History of chronic pain and severe degenerative spine disease with or without chronic pain
- History of drug addiction or dependency
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Spinal Cord StimulationSpinal Cord stimulation. Surgery is done in local anaesthesia. A small electrode is placed in the epidural space corresponding approximately at the Th8-Th10 level. An impulsegenerator, connected to the electrode, is placed in the subcutaneus fat in the gluteal region. | Device | Active, Placebo |
Primary outcome
Clinical improvement of gait
Time frame: Follow-up at 6 and 12 months
To establish proof of concept by changes in Postural Instability and Gait Difficulty (PIGD) subscore of the Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS UPDRS). This subscore is the sum of 2.12 (Walking and balance), 2.13 (Freezing), 3.10 (Gait), 3.11 (Freezing of gait) and 3.12 (Postural stability)
Changes in resting metabolic networks assessed with 18-FDG PET/CT
Time frame: Follow-up at 6 and 12 months
18-FDG is a tracer characterizing glucose metabolism. Quantification of 18F-FDG PET scans will be performed. Analysis of PET scans will be performed using both a region of interest (ROI) approach sampling hypothesized areas and exploratory Statistical Parametric Mapping (SPM). For each subject, ROIs will be defined on the individual CT and copied onto co-registered PET images. ROIs will include putamen, caudate nuclei, ventral striatum, thalamus, red nucleus, amygdala, hypothalamus, locus coeruleus, median raphe and the ventral tegmental area. SPM will allow automated interrogation of parametric images across the whole brain volume at a voxel level to localize significant differences in tracer uptake without a priori selection of target regions. The primary end points are the between-group differences in striatal and extrastriatal tracer uptake/binding.
Changes in brain cholinergic function
Time frame: Follow-up at 6 and 12 months
([18F]FEOBV) PET is an in vivo marker of the brain vesicular acetylcholine transporter (VAChT) and provides information of the integrity of the brain cholinergic neurotransmitter system. Quantification of 18FEOBV scans will be performed. Analysis of PET scans will be performed using both a region of interest (ROI) approach sampling hypothesized areas and exploratory Statistical Parametric Mapping (SPM). For each subject, ROIs will be defined on the individual CT and copied onto co-registered PET images. ROIs will include putamen, caudate nuclei, ventral striatum, thalamus, red nucleus, amygdala, hypothalamus, locus coeruleus, median raphe and the ventral tegmental area. SPM will allow automated interrogation of parametric images across the whole brain volume at a voxel level to localize significant differences in tracer uptake without a priori selection of target regions. The primary end points are the between-group differences in striatal and extrastriatal tracer uptake/binding.
Adverse events
Time frame: 6 and 12 months
Evaluation of the safety and tolerability of SCS treatment in patients with PD. Measured as type, frequency and severity of adverse events.
9 secondary outcomes
subjective changes in quality of life per SF-36
Time frame: Follow-up at 6 and 12 months
subjective changes in parkinsons specific quality of life
Time frame: Follow-up at 6 and 12 months
Clinical improvement of gait as measured by TUG in s
Time frame: Follow-up at 6 and 12 months
subjective changes in gait function
Time frame: Follow-up at 6 and 12 months
subjective changes in occurence of freezing
Time frame: Follow-up at 6 and 12 months
Overall Changes in PD severity
Time frame: Follow-up at 6 and 12 months
Improvement in home based gait ability
Time frame: Follow-up at 6 and 12 months
Changes in cognitive function as assessed by moca
Time frame: Follow-up at 6 and 12 months
Clinical improvement of balance as measured by BBS
Time frame: Follow-up at 6 and 12 months
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 May 2025.
- Derived from this study: PubMed 41611672Terkelsen MH, Hvingelby VS, Johnsen EL, Moller M, Danielsen EH, Henriksen T, Glud AN, Tai Y, Baun AM, Knudsen AL, Valdemarsen RN, Horsager J, Okkels N, Andersen ASM, Meier K, Borghammer P, Molloy S, Nandi D, Moro E, Sorensen JCH, Pavese N. Spinal cord stimulation therapy for gait impairment in Parkinson's disease: a double-blinded, randomised feasibility trial with an open extension. Nat Commun. 2026 Jan 29;17(1):2168. doi: 10.1038/s41467-026-68782-w.
- Derived from this study: PubMed 36101543Hvingelby VS, Hojholt Terkelsen M, Johnsen EL, Moller M, Danielsen EH, Henriksen T, Glud AN, Tai Y, Moller Andersen AS, Meier K, Borghammer P, Moro E, Sorensen JCH, Pavese N. Spinal cord stimulation therapy for patients with Parkinson's disease and gait problems (STEP-PD): study protocol for an exploratory, double-blind, randomised, placebo-controlled feasibility trial. BMJ Neurol Open. 2022 Aug 24;4(2):e000333. doi: 10.1136/bmjno-2022-000333. eCollection 2022.
- Individual participant dataSharing planned: Yes. As a significant amount of imaging data will be collected over the course of this trial, this data may be made available upon request based upon the relevance and scientific merit of the request.
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Parkinson Disease
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Nicola Pavese, MD, PhD, FRCP, FEAN principal investigator
University of Aarhus
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Spinal Cord Stimulation in people with Parkinson Disease and Gait Disorders, Neurologic, run by University of Aarhus at 1 site in Denmark.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 23 May 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Denmark. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Clinical improvement of gait (time frame: Follow-up at 6 and 12 months). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT05110053, which also lists 2 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 May 2025.