Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Movement Disorders from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 25
- Active, not recruiting: 6
- Completed: 13
- Other: 6
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00001252 — Human Movement Database
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institutes of Health Clinical Center (CC) |
| Enrollment | 7500 |
| Study Type | OBSERVATIONAL |
| Conditions | Movement Disorder |
This study will collect information on the different ways people control limb and body movements. This information will be used to develop a database on normal movements and adaptive movements of people who have diseases that affect the way they move. The database will serve as a tool to improve diagnosis and treatment of patients with movement-related problems.
Volunteers from one month old t…
NCT02014246 — Genetic Characterization of Movement Disorders and Dementias
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute on Aging (NIA) |
| Enrollment | 12000 |
| Study Type | OBSERVATIONAL |
| Conditions | Dementia; Movement Disorder |
Background:
There are two basic types of movement disorders. Some cause excessive movement, some cause slowness or lack of movement. Some of these are caused by mutations in genes. On the other hand, dementia is a condition of declining mental abilities, especially memory. Dementia can occur at any age but becomes more frequent with age. Researchers want to study the genes of families with a h…
NCT01581580 — Deep Brain Stimulation Surgery for Movement Disorders
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson’s Disease; Essential Tremor; Dystonia |
| Interventions | ; |
Background:
- Deep brain stimulation (DBS) is an approved surgery for certain movement disorders, like Parkinson’s disease, that do not respond well to other treatments. DBS uses a battery-powered device called a neurostimulator (like a pacemaker) that is placed under the skin in the chest. It is used to stimulate the areas of the brain that affect movement. Stimulating these areas helps to b…
NCT01682668 — Subthalamic Nucleus, Akinesia and Parkinson’s Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Institut National de la Santé Et de la Recherche Médicale, France |
| Enrollment | 180 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson’s Disease |
| Interventions |
This program aims to understand the role of the subthalamic nucleus in the control of the movement in healthy humans and patients with Parkinson’s disease, how the STN dysfunction contributes to akinesia and how the STN stimulation improves motor signs in PD patients .
NCT02071134 — Registry of Deep Brain Stimulation With the VERCISE™ System: Vercise DBS Registry
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Boston Scientific Corporation |
| Enrollment | 1500 |
| Study Type | OBSERVATIONAL |
| Conditions | Parkinson’s Disease |
| Interventions |
The purpose of this registry is to compile characteristics of world-wide outcomes for the use of Boston Scientific’s commercially available Vercise DBS System in the treatment of Parkinson’s disease.
The utilization of Image Guided Programming (IGP), and other commercially available programming features, used as planning tools for the programming of patients with Boston Scientific’s Vercise DB…
NCT04032470 — Boston Scientific Registry of Deep Brain Stimulation for Treatment of Essential Tremor (ET)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Boston Scientific Corporation |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | Essential Tremor |
| Interventions |
To compile characteristics of real-world outcomes for Boston Scientific Corporation’s commercially approved Deep Brain Stimulation (DBS) Systems, when used according to the applicable Directions for Use, for the treatment of Essential Tremor.
NCT06553625 — Radiofrequency (RF) Ablation Prospective Outcomes Study for Central Nervous System - RAPID for CNS
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Boston Scientific Corporation |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Parkinson Disease; Dystonia; Essential Tremor; Movement Disorders |
| Interventions |
The objective of this study is to compile real-world outcomes of Boston Scientific commercially approved radiofrequency (RF) ablation systems used in the central nervous system (CNS) for use in functional neurosurgery.
NCT06087926 — Apathy in Parkinson Disease TMS Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of North Carolina, Chapel Hill |
| Enrollment | 100 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson Disease |
| Interventions |
The goal of this clinical trial is to develop non-invasive brain stimulation targets for the treatment of apathy, or motivation problems, in Parkinson Disease.
The main questions the study aims to answer are:
- Does transcranial magnetic stimulation change effort task performance in Parkinson’s Disease patients?
- Is there a link between brain signals and apathy?
Participants will
- compl…
NCT06464029 — Pathways Mediating Impaired Postural Control in Parkinson’s Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Minnesota |
| Enrollment | 160 |
| Study Type | OBSERVATIONAL |
| Conditions | Parkinson Disease |
The purpose of this project is to use transcranial magnetic stimulation (TMS) to explore the state of excitability of corticocortical and corticofugal (cortex to spinal cord, cortex to brainstem to spinal cord) pathways that project to muscles that control the legs and trunk in people with Parkinson’s disease. The outcome variables will be further analyzed to understand their relationship to qu…
NCT07094269 — Protocol of the Packer Managing Fatigue Program Versus Standard Information to Improve Energy Conservation Self-Efficacy in Parkinson’s Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Universita degli Studi di Genova |
| Enrollment | 80 |
| Study Type | INTERVENTIONAL |
| Conditions | PARKINSON DISEASE (Disorder) |
| Interventions | ; |
This protocol describes a randomized, controlled, parallel-group, trial evaluating the effectiveness of a group-based fatigue management program for people with Parkinson’s disease. The study will be conducted in Italy, with participant recruitment planned to begin on July 1st, 2025. The primary sponsor is the Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics and Maternal Chil…
NCT06920134 — Epidural Electrical Stimulation to Support Hemodynamic Management in Individuals With Parkinson’s Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Ecole Polytechnique Fédérale de Lausanne |
| Enrollment | 5 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypotension Symptomatic; Parkinson’s Disease; Orthostatic Hypotension, Dysautonomic; Multiple System Atrophy (MSA) With Orthostatic Hypotension; Multiple System Atrophy - Parkinsonian Subtype (MSA-P) |
| Interventions |
The PD-HemON study aims to evaluate the safety and preliminary efficacy of ARC-IM Therapy (Epidural Electrical Stimulation) to support hemodynamic management in people with typical and atypical Parkinson’s Disease, who suffer from orthostatic hypotension.
NCT07197866 — An Extension Trial to Test if TEV-56286 is Effective in Relieving Multiple System Atrophy
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Teva Branded Pharmaceutical Products R&D LLC |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Multiple System Atrophy |
| Interventions |
The primary objective of the trial is to describe the long-term safety and tolerability of TEV-56286 administered orally for the treatment of adult participants with Multiple System Atrophy (MSA).
A secondary objective of the trial is to further describe the safety and tolerability of TEV-56286.
The planned total duration of the trial is approximately 100 weeks.
NCT07115563 — Daily Amino Acid Supplementation for People With Parkinson’s Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Cristina Colon-Semenza |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson Disease (PD) |
| Interventions | ; |
The goal of this clinical trial is to learn if a tailored amino acid supplement works to help adults living with Parkinson’s disease to improve nutrition, metabolic function, body composition, and physical and mental function. The main questions it aims to answer are:
Does the tailored amino acid supplement increase essential amino acids (nutritional status)?
Does the tailored amino acid supp…
NCT07174310 — A Study to Evaluate the Efficacy and Safety of Intravenous (IV) Prasinezumab in Participants With Early-Stage Parkinson’s Disease
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Hoffmann-La Roche |
| Enrollment | 900 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson’s Disease |
| Interventions | ; |
The purpose of this study is to evaluate the efficacy, safety, and pharmacokinetics (PK) of prasinezumab compared with placebo in participants with early-stage Parkinson’s disease (PD) on stable symptomatic monotherapy with levodopa.
NCT06857851 — Optimizing Deep Brain Stimulation to Improve Visuomotor Function in Parkinson’s Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | VA Office of Research and Development |
| Enrollment | 80 |
| Study Type | OBSERVATIONAL |
| Conditions | Parkinson’s Disease |
Inability to align and refocus the eyes on the objects at different depths, i.e., vergence impairment and strabismus, frequently affects the quality of life in patients with Parkinson’s disease. The investigators study aims to understand the location-specific effects of subthalamic region deep brain stimulation on vergence and strabismus by integrating the patient-specific deep brain stimulatio…
NCT07428447 — Analysis of Cutaneous Phosphorylated Alpha-Synuclein to Identify Patients at Risk of Progressing From Essential Tremor to Parkinson’s Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | CND Life Sciences |
| Enrollment | 300 |
| Study Type | OBSERVATIONAL |
| Conditions | Essential Tremor, Movement Disorders; Essential Tremor; Essential Tremor-plus |
Background and Rationale Essential tremor (ET) affects over 6 million Americans and approximately 5% of adults over age 60. Patients with ET have a 10-20 times higher risk of developing Parkinson’s disease (PD) compared to age-matched populations, with approximately 1% converting to PD annually. Post-mortem studies reveal Lewy body pathology in some ET patients, suggesting a subset may have pro…
NCT07221669 — A Study to Learn About Salanersen’s (BIIB115) Effects on Movement and Its Safety When Given Before Symptoms Appear in Babies With Genetically Diagnosed Spinal Muscular Atrophy (SMA)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Biogen |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Muscular Atrophy, Spinal |
| Interventions |
In this study, researchers will learn more about the effects and safety of BIIB115, also known as salanersen.
Specifically, researchers will learn more about how salanersen works in babies who have been diagnosed with SMA through genetic testing but have not yet started showing signs or symptoms. Most people with SMA have changes in a gene called survival motor neuron 1, also known as SMN1. Th…
NCT07682532 — L-THEANINE AND MEDITERRANEAN DIET ON RBD, GI FUNCTION, AND INFLAMMATION IN PARKINSON’S DISEASE
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Medipol University |
| Enrollment | 52 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson Disease (PD) |
| Interventions | ; |
Parkinson’s disease is a progressive neurological disorder associated with severe dopaminergic neuron loss in the substantia nigra pars compacta. The decrease in dopamine cells in the gut in Parkinson’s disease negatively affects bowel movements, and constipation is a common condition. Impairment of the intestinal barrier increases inflammation. Reactive oxygen species increase, and intestinal …
NCT07410598 — Safety and Tolerability of Patterned Stimulation for DBS in the Home Setting
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Florida |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson Disease; Deep Brain Stimulation |
| Interventions | ; ; |
The primary objective of the proposed pilot study is to assess the safety and tolerability of active patterned Deep Brain Stimulation (pDBS) when administered in a home setting for patients with Parkinson’s disease (PD) who have had stable bilateral Subthalamic Nucleus (STN) and Globus Pallidus internus (GPi) DBS.
NCT07213219 — PET-MRI of Reward System in Parkinson’s Disease With RBD
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University Hospital, Clermont-Ferrand |
| Enrollment | 44 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson's Disease (PD) |
| Interventions |
Impulse control disorders (ICDs) are frequently observed in Parkinson’s disease (PD) and can have a major functional impact on the quality of life of both the patient and their entourage. The primary risk factor for the emergence of ICDs in PD is long-term dopaminergic treatment, but other risk factors, such as rapid eye movement sleep behavior disorder (RBD), have recently been identified. The…
NCT07589595 — A Study of Donanemab (LY3002813) in Participants With Early Cognitive Decline (TRAILBLAZER-ALZ 7)
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Eli Lilly and Company |
| Enrollment | 350 |
| Study Type | INTERVENTIONAL |
| Conditions | Cognitive Dysfunction; Lewy Body Disease; Synucleinopathies; Amyloid |
| Interventions | ; |
The main purpose of this study is to evaluate whether treatment with donanemab slows the progression of cognitive (how we think, learn, remember, pay attention, and make decisions) and functional (how we are able to perform daily activities) decline. For each participant, the study will last one and a half years.
NCT07381751 — Artificial Intelligence-assisted MDS-UPDRS Assessment for Parkinson’s Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Hong Kong University of Science and Technology |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | Parkinson Disease |
| Interventions |
Idiopathic Parkinson’s disease (PD) is a neurodegenerative disease that progressively causes both motor and non-motor symptoms. As the second most common neurodegenerative disease and most common movement disorder, it affects over 8.5 million people worldwide and 13,000 people in Hong Kong. The most classical symptoms of PD are resting tremors, rigidity of the muscles, bradykinesia (slowing of …
NCT06997198 — Deutetrabenazine Treatment for Tardive Dyskinesia in Intellectual/Developmental Disabilities
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | University Hospitals Cleveland Medical Center |
| Enrollment | 25 |
| Study Type | INTERVENTIONAL |
| Conditions | Tardive Dyskinesia; Intellectual Disability; Developmental Disabilities |
| Interventions |
The primary goal of this study is to investigate the efficacy of deutetrabenazine treatment of TD in this previously untreated patient population. Compare movement disorder deutetrabenazine treatment response in persons with IDD to response seen in patients without IDD treated with deutetrabenazine in other treatment settings (per literature review). Compare global deutetrabenazine treatment re…
NCT07685873 — Monoamine Oxidase B PET/CT in Various MAO-B-Related Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Tianjin Medical University |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Parkinson Disease; Parkinson Disease Dementia; Parkinson’s Disease and Parkinsonism |
| Interventions |
To evaluate the potential usefulness of 18F-FPyCO/SMBT-1 positron emission tomography/computed tomography (PET/CT) for the diagnosis of primary and metastatic lesions in various MAO-B-related disease patients.
NCT07641556 — The Effects of Tele-Rehabilitation-Based Dual-Task Upper Extremity Training in Patients With Parkinson’s Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Saglik Bilimleri Universitesi |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson’s Disease (PD) |
| Interventions | ; ; |
The aim of this study is to compare the effects of tele-rehabilitation-based synchronous and asynchronous dual-task upper extremity training with clinical based dual-task upper extremity training and conventional single-task upper extremity training in patients with Parkinson’s disease. The main questions it aims to answer are:
- Whether there are differences in motor symptoms, hand dexterity,…
Active, Not Recruiting
NCT00001246 — Brain Imaging of Childhood Onset Psychiatric Disorders, Endocrine Disorders and Healthy Volunteers
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Institute of Mental Health (NIMH) |
| Enrollment | 4274 |
| Study Type | OBSERVATIONAL |
| Conditions | Attention Deficit Hyperactivity Disorder; Schizophrenia; Attention Deficit Disorder With Hyperactivity |
Magnetic Resonance Imaging (MRI) unlike X-rays and CT-scans does not use radiation to create a picture. MRI use as the name implies, magnetism to create pictures with excellent anatomical resolution. Functional MRIs are diagnostic tests that allow doctors to not only view anatomy, but physiology and function. It is for these reasons that MRIs are excellent methods for studying the brain.
In th…
NCT02305147 — Cohort Study to Identify Predictor Factors of Onset and Progression of Parkinson’s Disease
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Institut National de la Santé Et de la Recherche Médicale, France |
| Enrollment | 385 |
| Study Type | OBSERVATIONAL |
| Conditions | Parkinson Disease |
| Interventions |
Observational, prospective, monocentric study to assess clinical features, imaging and biologic biomarkers in Parkinson disease (PD) patients and rate of progression compared to healthy controls (HC) and subjects at risk to develop PD.
The primary objective of this study is to identify clinical, imaging and biologic markers of PD onset and progression for use in clinical trials of disease-modi…
NCT02632422 — AIH-induced Walking Recovery After Subacute SCI
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Spaulding Rehabilitation Hospital |
| Enrollment | 125 |
| Study Type | INTERVENTIONAL |
| Conditions | Spinal Cord Injury |
| Interventions | ; ; |
The purpose of this study is to determine how mild breathing bouts of low oxygen may restore walking and leg strength in persons who have sustained a spinal cord injury.
NCT02994719 — Gait Analysis in Neurological Disease
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Beth Israel Deaconess Medical Center |
| Enrollment | 120 |
| Study Type | OBSERVATIONAL |
| Conditions | Parkinson’s Disease; Parkinsonian Disorders; Atypical Parkinson Disease; Progressive Supranuclear Palsy; Multiple System Atrophy |
| Interventions | ; |
The purpose of this study is to investigate whether speed-dependent measures of gait (so called gait signatures) can be identified in patients with neurological conditions that affect gait, particularly in subjects with parkinsonian disorders.
NCT03648905 — Clinical Laboratory Evaluation of Chronic Autonomic Failure
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 89 |
| Study Type | OBSERVATIONAL |
| Conditions | Parkinson’s Disease; Multiple System Atrophy; Autonomic Failure |
| Interventions | ; ; |
Background:
The autonomic nervous system controls automatic body functions. Researchers want to improve the tests used to diagnose autonomic failure. Orthostatic hypertension is a drop in blood pressure when a person stands up. Researchers want to focus on this sign of autonomic failure.
Objective:
To improve testing for conditions that cause autonomic nervous system failure.
Eligibility:
…
NCT05808504 — Investigation of the Benefits of Electrical Non-invasive Stimulation on Cognitive Symptoms in Parkinson’s Disease
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Institut National de la Santé Et de la Recherche Médicale, France |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson Disease |
| Interventions | ; ; |
Parkinson’s disease is the second most common neurodegenerative disease after Alzheimer’s disease.
It is mostly characterized by the presence of motor difficulties. However, it can also be accompanied by cognitive disorders which have an equally significant impact on the quality of life of patients and which are not relieved by any treatment.
Among the functions affected by Parkinson’s diseas…
Not Yet Recruiting
NCT07685444 — A Clinical Study to Evaluate the Safety, Tolerability, and Efficacy of Intracerebral Injection of LY-N001 Injection for the Treatment of Moderate to Advanced Parkinson’s Disease With GBA1 Mutations
| Status | Not yet recruiting |
| Phase | Early Phase 1 |
| Sponsor | Lingyi Biotech Co., Ltd. |
| Enrollment | 18 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson’s Disease (PD) |
| Interventions |
This is a prospective, single-arm, single-dose clinical study designed to evaluate the safety, tolerability, efficacy, immunogenicity, pharmacodynamic (PD) and pharmacokinetic (PK) profiles of LY-N001 Injection in patients with moderate-to-advanced Parkinson’s disease carrying GBA1 mutations. The study consists of a main study phase and a long-term follow-up phase.
NCT07688525 — Pain Beliefs and Intracortical Excitability During Experimental Pain
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Université de Sherbrooke |
| Enrollment | 30 |
| Study Type | INTERVENTIONAL |
| Conditions | Kinesiophobia (Fear of Movement); Experimental Pain |
| Interventions |
Pain can influence the way the motor system functions. However, responses to pain vary widely between individuals, and this variability may be partly related to pain-related beliefs such as kinesiophobia.
This study examines whether temporary experimental pain changes intracortical excitability in the motor cortex, and whether this response differs according to baseline kinesiophobia. Healthy …
NCT07673146 — Probing Gut-Brain Communication in Parkinson’s Disease
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Spaulding Rehabilitation Hospital |
| Enrollment | 45 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson Disease (PD) |
| Interventions | ; |
Administering transcutaneous vagus nerve stimulation in patients with Parkinson’s disease to see how it affects stomach and brain activity.
NCT07683455 — Retrospective Study of Intensive Therapy Pathways in Children With Cerebral Palsy (P’TI-PARCOURS)
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Centre Médico-Chirurgical de Réadaptation des Massues Croix Rouge Française |
| Enrollment | 75 |
| Study Type | OBSERVATIONAL |
| Conditions | Cerebral Palsy; Hemiplegia |
| Interventions |
This retrospective single-center study aims to describe the care pathways of children with unilateral cerebral palsy (hemiplegia) who participated in intensive therapy programs (COLHEMI and/or Mini-COLHEMI) at the Centre des Massues since January 2010. The COLHEMI program (launched in 2010, for children aged 6-12) provides 70 hours of intensive motor learning-based therapy over 2 weeks, while t…
NCT03794726 — Comparison of Orthodontic Molar Protraction With and Without Adjunctive Surgery
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | University of Alabama at Birmingham |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Malocclusion |
| Interventions | ; |
This study will compare orthodontic molar protraction with and without adjunctive periodontally accelerated osteogenic orthodontic (PAOO) surgery prior to orthodontic tooth movement.
To the investigators’ knowledge, this type of molar retraction in adult patients has not been compared with and without the adjunctive use of PAOO for differences in clinical linear tooth movement and patient cent…
Enrolling by Invitation
NCT07525973 — The Effect of Eye Exercises in Parkinson’s Disease
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | Pardis Specialized Wellness Institute |
| Enrollment | 34 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson Disease |
| Interventions |
Parkinson’s disease is commonly associated with impaired gait, postural instability, reduced physical function, and increased concern about falling, all of which contribute substantially to disability and reduced quality of life. Exercise-based rehabilitation is increasingly recommended as a core non-pharmacological strategy for improving mobility and balance in people with Parkinson’s disease….
Completed Trials
NCT01496599 — Imaging Biomarkers in Parkinson s Disease
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 62 |
| Study Type | OBSERVATIONAL |
| Conditions | Parkinson Disease |
Background:
- Parkinson s disease (PD) causes slow movement, stiffness, and tremor. It results from the loss of a brain chemical called dopamine. PD gets worse over time, but researchers do not fully understand why the brain cells that produce dopamine stop working or die in people with PD. This study will use different ways of imaging the brain and brain chemicals to look at PD. It will comp…
NCT02800460 — New Approaches in MRI at 3T Dedicated to Targeting Subthalamic Nucleus on Parkinsonian Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | Institut National de la Santé Et de la Recherche Médicale, France |
| Enrollment | 105 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson Disease |
| Interventions |
Deep brain stimulation (DBS) of the subthalamic nucleus (STN) is a validated procedure, used in many French and international centers for the treatment of severe forms of Parkinson’s disease (PD). The improvement of parkinsonian motor symptoms by stimulation of the STN is 50 to 80% on average. The main advantage of DBS is that the surgery has low morbidity and mortality, it is adaptable to the …
NCT05036473 — A Study of the Efficacy and Safety of Carbidopa-Levodopa Extended-Release Tablets in Patients With Parkinson’s Disease
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Shanghai WD Pharmaceutical Co., Ltd. |
| Enrollment | 40 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson Disease |
| Interventions | ; |
It is a phase II randomized, parallel, double-blind, placebo-controlled, multi-center clinical trial of the efficacy and safety of WD-1603 Carbidopa-Levodopa Extended-Release Tablets in patients with Parkinson’s disease. The objective of the study is to access the safety and efficacy of WD-1603 carbidopa-levodopa extended-release tablets in patients with Parkinson’s disease.
NCT05298150 — Remote Dynamic Cycling for the Customized Off-site Rehab in Parkinson’s Disease
| Status | Completed |
| Phase | N/A |
| Sponsor | VA Office of Research and Development |
| Enrollment | 60 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson’s Disease |
| Interventions | ; |
This research will develop novel and accessible way to deliver effective and customized rehab to those suffering from common and devastating neurodegenerative condition called Parkinson’s disease. The investigators will examine the efficacy of novel rehab technique that can be monitored and modified in real-time but over virtual interface using a remotely located device in a paradigm called dyn…
NCT07685392 — Progressive Strength and Balance Exercise for Fall Prevention in Postmenopausal Women With Osteoporosis
| Status | Completed |
| Phase | N/A |
| Sponsor | Instituto Nacional de Rehabilitacion |
| Enrollment | 46 |
| Study Type | INTERVENTIONAL |
| Conditions | Postmenopausal Osteoporosis; Accidental Falls, Aged, Exercise Movement Techniques; Fragility Fractures |
| Interventions | ; |
Postmenopausal osteoporosis increases the risk of fragility fractures, and falls are a major modifiable pathway leading to fracture. This single-blind randomized controlled pilot trial evaluated whether a supervised progressive strength and balance exercise program reduced fall occurrence compared with a conventional home-based exercise program in postmenopausal women with osteoporosis. Women a…
NCT07687732 — Vibrotactile Stimulation for Parkinson’s Disease
| Status | Completed |
| Phase | Early Phase 1 |
| Sponsor | University of Colorado, Denver |
| Enrollment | 12 |
| Study Type | INTERVENTIONAL |
| Conditions | PARKINSON DISEASE (Disorder) |
| Interventions |
Investigation on whether and how vibrotactile stimulation applied on the fingertips affects beta power in the subthalamic nucleus.
NCT06336252 — Technology Assisted Nudging to Increase Physical Activity Among Hospitalised Medical Patients
| Status | Completed |
| Phase | N/A |
| Sponsor | Bispebjerg Hospital |
| Enrollment | 130 |
| Study Type | INTERVENTIONAL |
| Conditions | COPD; Heart Failure; Parkinson Disease; Arthritis; Old Age; Cachexia |
| Interventions |
Primary Objective To investigate if patients hospitalised for older adults with a decreased level of physical function, either related to a chronic condition e.g., COPD, Congestive heart failure, renal failure; infections; frailty and tendency of falling; orthopaedic surgery - after hip fracture will increase their time spent out of bed during hospitalisation and 3 months after discharge throug…
NCT06329141 — A Study to Assess the Efficacy and Safety of Vutiglabridin in Early Parkinson’s Disease Patients
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | Glaceum |
| Enrollment | 99 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson Disease |
| Interventions | ; |
Study Objective
- To assess the efficacy and safety of vutiglabridin in early Parkindson’s disease patients
Background Glaceum Inc. has evaluated the safety, tolerability, and pharmacokinetic/pharmacodynamic properties of vutiglabridin in healthy subjects through its Phase 1 trials, and is planning to perform this Phase 2a trial to assess the efficacy and safety of vutiglabridin in e…
NCT06815965 — A Clinical Study of Neflamapimod in Patients With Dementia With Lewy Bodies
| Status | Completed |
| Phase | Phase 2 |
| Sponsor | EIP Pharma Inc |
| Enrollment | 26 |
| Study Type | INTERVENTIONAL |
| Conditions | Dementia With Lewy Bodies (DLB) |
| Interventions |
The purpose of this clinical study is to evaluate the safety and tolerability (side effects) and pharmacokinetics (drug levels in the body) of 80mg neflamapimod given twice daily in patients with dementia with Lewy bodies.
NCT07683130 — Comparative Effects of Mirror Therapy, Proprioceptive Neuromuscular Facilitation, and Constraint-Induced Movement Therapy on Upper Limb Motor Recovery in Stroke Survivors: A Three-Arm Randomized Controlled Trial
| Status | Completed |
| Phase | N/A |
| Sponsor | Foundation of Medical Research and Laboratories, Pakistan |
| Enrollment | 90 |
| Study Type | INTERVENTIONAL |
| Conditions | Stroke |
| Interventions | ; ; |
This study aimed to compare the effects of these three interventions on upper limb motor recovery in stroke survivors.
A three-arm randomized controlled trial was conducted in which eligible participants (N=90) with post-stroke upper limb hemiparesis were randomly allocated into three groups of 30 each: MT group, PNF group, and CIMT group. All groups received their respective interventions alo…
NCT07636603 — Pain-Related Fear and Motor Control in Healthy Volunteers
| Status | Completed |
| Phase | N/A |
| Sponsor | Universite de Picardie Jules Verne |
| Enrollment | 26 |
| Study Type | INTERVENTIONAL |
| Conditions | Pain-related Fear; Kinesiophobia (Fear of Movement); Movement-Related Threat |
| Interventions | ; |
The goal of this clinical trial is to learn how experimentally induced movement-related threat affects emotional, autonomic, and motor responses in healthy adults. The main questions it aims to answer are:
- Does movement-related threat change walking performance or upper-limb pointing movements?
- Are these effects moderated by participants’ level of kinesiophobia?
- Does movement-related thr…
NCT07264114 — Aquatic High-Intensity Interval Training for Parkinson’s Disease
| Status | Completed |
| Phase | N/A |
| Sponsor | Pardis Specialized Wellness Institute |
| Enrollment | 56 |
| Study Type | INTERVENTIONAL |
| Conditions | Parkinson Disease |
| Interventions |
This randomized, single-center, parallel-group superiority trial will evaluate the effect of an 8-week aquatic High-Intensity Interval Training (HIIT) program on balance, physical function, and sarcopenia-related outcomes in individuals with Parkinson’s disease (PD). The intervention aims to deliver Tabata-style aquatic HIIT (3 sessions/week) in a therapeutic pool to determine adherence and pre…
NCT07587476 — Constraint-induced Movement Therapy Combined With Functional Electrical Stimulation in Children With Cerebral Palsy
| Status | Completed |
| Phase | N/A |
| Sponsor | Montiha Azeem |
| Enrollment | 46 |
| Study Type | INTERVENTIONAL |
| Conditions | Cerebral Palsy (CP) |
| Interventions | ; |
This randomized controlled trial aims to compare the effectiveness of Constraint-Induced Movement Therapy (CIMT) combined with Functional Electrical Stimulation (FES) versus CIMT alone in improving upper limb function, reducing spasticity, and enhancing functional independence in children with cerebral palsy (CP). A total of 46 children aged 3 to 15 years with spastic or dyskinetic cerebral pal…