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NCT ID: NCT05810454 Not yet recruiting - Parkinson's Disease Clinical Trials

iPACES v3 MCI NIA Protocol Copied for iPACES v4 PD NINDS

iPACES-PD
Start date: August 2023
Phase: N/A
Study type: Interventional

The primary purpose of this study is to attempt to replicate and extend promising pilot findings regarding the cognitive benefits of in-home neuro-exergaming with iPACES (interactive Physical and Cognitive Exercise System v3) for persons with mild cognitive impairment (MCI), to evaluate effects for persons with Parkinson's Disease (PD). Participants will include persons with PD, and potentially, also their co-residing partner, who will exercise at home or accessible location, 3-5 times per week for at least 6 months, with follow-up one month after the main intervention. All participation is "remote" (completed at home, or location of choice), utilizing either one's own equipment ("bring-your-own-devices" BYODs: pedaler, phone/tablet, smart-watch) or some equipment which may be supplied by the grant-funded study and shipped directly to the home; all study measures are completed remotely (e.g., via phone app, website, biometric device, videoconference, email, snail mail, etc.).

NCT ID: NCT03021408 Recruiting - Rehabilitation Clinical Trials

Effectiveness of Different Approaches for the Rehabilitation of Gait in Patients With Parkinson's Disease

Tr-T-VR
Start date: January 2017
Phase: N/A
Study type: Interventional

Evaluation of the effectiveness of three different approaches for the rehabilitation of gait in patients with PD within a multidisciplinary, intensive rehabilitation treatment (MIRT).

NCT ID: NCT01807481 Recruiting - PD Clinical Trials

Phase IV Study to Evaluate the Efficacy and Safety of Mircera in PD

Start date: March 2013
Phase: Phase 4
Study type: Interventional

The primary objective of study is to evaluate the no of patients which maintain the Hb level between 9.0 ~ 12.0 g/dl during the evaluation period

NCT ID: NCT00561678 Completed - Clinical trials for Postoperative Delirium

Perioperative Cognitive Function - Dexmedetomidine and Cognitive Reserve

Start date: February 2008
Phase: Phase 4
Study type: Interventional

Elderly patients who undergo anesthesia and non-cardiac surgery are subject to deterioration of brain function including the development of postoperative delirium (PD) and postoperative cognitive dysfunction (POCD). These disorders cause disability, distress for both patients and their families, are associated with other medical complications and account for significant additional health care costs. We currently use relatively primitive approaches to preventing and treating PD and POCD. Dexmedetomidine is a drug used for sedation in critically ill patients that provides some pain relief and controls the bodies response to stress. The sedation produced by dexmedetomidine appears more similar to natural sleep than any other drug used for anesthesia and postoperative sedation. Data suggesting that dexmedetomidine can prevent delirium following cardiac surgery and the developing understanding of the causes of PD and POCD suggest that dexmedetomidine will be particularly effective.

NCT ID: NCT00455143 Terminated - Clinical trials for Postoperative Delirium

Cognitive Protection - Dexmedetomidine and Cognitive Reserve

Start date: September 2006
Phase: Phase 4
Study type: Interventional

This is a pilot study to evaluate the effect of dexmedetomidine in the prevention of delirium in non-cardiac surgical patients. The preliminary data regarding the effect of dexmedetomidine on delirium comes from a study underway at Stanford. We propose to randomize fifty patients into two different protocols, one using dexmedetomidine until PACU discharge (hip replacement) and the other using dexmedetomidine for 24 hours in a monitored setting.

NCT ID: NCT00105131 Completed - Parkinson Disease Clinical Trials

Genetic Characterization of Parkinson's Disease

Start date: March 2005
Phase: N/A
Study type: Observational

This study will explore the risks and causes of Parkinson's disease, a chronic progressive nervous system disorder. Patients typically have tremors, muscle weakness and a shuffling gait. Patients with Parkinson's disease, their relatives and healthy volunteers may be eligible for this study. Candidates must be 18 years of age or older. Patients whose parkinsonism is due to a secondary cause, such as infection or injury, and healthy volunteers who have a first degree family member (parent, grandparent, child, sibling) with Parkinson's disease are excluded from enrollment. Participants are asked about possible symptoms they may have and about their general health. They provide a blood sample to obtain DNA for genetic analysis to look for genetic differences that might be related to risks for Parkinson's disease. White blood cells may be treated in the laboratory to grow a cell line, which provides a source of substances in the blood without having to draw samples repeatedly.