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Parkinson Disease clinical trials

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NCT ID: NCT02727257 Completed - Parkinson's Disease Clinical Trials

The Effect of a Motor-cognitive Rehabilitation on Attention in Parkinsonian Patients

Start date: January 2015
Phase: N/A
Study type: Interventional

In this study the Investigators explore two questions: if the attentive reaction times differs in parkinsonian patients from health controls and if an intensive, focused and aerobic rehabilitation program (Multidisciplinary Intensive Rehabilitation Treatment - MIRT) tailored mainly for motor problems, could have a specific positive effect on multiple choices Reaction Times (RTs) as an indirect marker for an effect on attentional-executive frontal circuits. The hypothesis is that the MIRT could have a positive effect on the top-down control mechanisms, since the continuous feedback given by physiotherapist during exercises and the use of cues and devices (such as treadmill plus and stabilometric platform), stimulate the selective attention processes that enable goal-directed, internally-driven decision, helping the patients to overcome externally-driven decision based on stimulus salience and novelty

NCT ID: NCT02723396 Completed - Clinical trials for Idiopathic Parkinson Disease

Sleep, Awake & Move - Part I

SA&M-I
Start date: March 16, 2016
Phase:
Study type: Observational

Sleep benefit (SB) is a prominent spontaneous, apparently unpredictable, transitory improvement in motor function reported by around 50% of patients affected by Parkinson's Disease (PD) after sleep and before taking their first dose of dopaminergic medications. This study aims at systematically characterizing SB in PD patients in an ecological setting and to explore the relationships between nocturnal and diurnal sleep and subjective and objective measures of motor function. A better understanding of this phenomenon is mandatory for future research on this topic.

NCT ID: NCT02722824 Completed - Parkinson's Disease Clinical Trials

Efficacy of a Non-invasive Device for Alleviation of Parkinson's Disease Symptoms

Start date: November 2015
Phase: N/A
Study type: Interventional

Investigation efficacy of a non-invasive wearable electrostimulator device where the supplementary motor area, premotor area and/or subthalamic nucleus are stimulated bilaterally and extracranially.

NCT ID: NCT02719496 Completed - Clinical trials for Gastrointestinal Disorders in Parkinson's Disease

Prove of Concept Study, to Evaluate the Efficacy, Safety, and Tolerability of IBEROGAST in the Treatment of Bowel Troubles in Patients With Parkinson's Disease

PHYTOPARK
Start date: April 2016
Phase: Phase 2
Study type: Interventional

The main objective of this study is to evaluate the efficacy of STW5 Iberogast, over a 28-day period, for the treatment of constipation in parkinsonian patients suffering from gastrointestinal disorders.

NCT ID: NCT02719470 Completed - Parkinson's Disease Clinical Trials

Does Cognitive Impairment Affect Rehabilitation Outcome in Parkinson's Disease?

Start date: January 2014
Phase: N/A
Study type: Interventional

In order to explore the question how an intensive, goal-based and aerobic rehabilitation treatment, addressed to act on motor and mental aspects, affects motor and functional symptoms in PD patients with normal cognition and with different level of cognitive impairment. Hypothesis is that a specific rehabilitation program based on motor-cognitive training and repetition, can affect positively the rehabilitation outcome regardless of baseline cognitive profile.

NCT ID: NCT02710487 Completed - Clinical trials for Idiopathic Parkinson's Disease

Sleep, Awake & Move - Part II

SA&M-II
Start date: March 3, 2016
Phase: N/A
Study type: Interventional

Sleep benefit (SB) is a prominent spontaneous, apparently unpredictable, transitory improvement in motor function reported by around 50% of patients affected by Parkinson's Disease (PD) after sleep and before taking their first dose of dopaminergic medications. The aim of this study is to test the hypothesis that objective and/or subjective improvement of motor function might be due to a carry-over effect of Rapid Eye Movements (REM) sleep at awakening from this sleep phase.

NCT ID: NCT02709148 Completed - Parkinson's Disease Clinical Trials

State-dependent Pathophysiological Oscillations in Parkinson's Disease and Treatment With Deep Brain Stimulation (DBS)

Start date: July 20, 2017
Phase: Phase 1
Study type: Interventional

The purpose of this study is to use an investigational device to record brain activity for 12-24 months following surgical implantation of deep brain stimulation (DBS) systems. The goal of the study is better understanding of brain activity in Parkinson's disease and how they relate to DBS and pharmacological management, not to bring new devices to market.

NCT ID: NCT02708186 Completed - Clinical trials for Dementia With Lewy Bodies

Study Evaluating Nelotanserin for Treatment of REM Sleep Behavior Disorder in Subjects With Dementia (DLB or PDD)

Start date: March 2016
Phase: Phase 2
Study type: Interventional

This study seeks to evaluate the safety and efficacy of Nelotanserin for the treatment of Rapid Eye Movement (REM) Sleep Behavior Disorder (RBD) in subjects with dementia with Lewy bodies (DLB) or Parkinson's disease dementia (PDD).

NCT ID: NCT02705755 Completed - Parkinson Disease Clinical Trials

TD-9855 Phase 2 in Neurogenic Orthostatic Hypotension (nOH)

Start date: September 9, 2017
Phase: Phase 2
Study type: Interventional

This multiple-center, 3-part, single-blind dose escalation (Part A), randomized, double-blind (Part B), and open-label multiple dose extension (Part C) study will be conducted in male and female subjects with neurogenic orthostatic hypotension to evaluate the effect of TD-9855 in improving symptoms of orthostatic intolerance.

NCT ID: NCT02705586 Completed - Parkinson's Disease Clinical Trials

Video Based Mindfulness Based Stress Reduction

vMBSR
Start date: March 2016
Phase: N/A
Study type: Interventional

To evaluate the feasibility of a video based mindfulness intervention for stress reduction and to evaluate the cortisol response in persons with PD and their caregivers. The data from this project will be used for a future grant application of a stress reduction intervention in persons with PD.