TERMINATED

Apraxia in Parkinson's Disease Patients With Deep Brain Stimulation

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Deep brain stimulation (DBS) of the subthalamic nucleus or globus pallidus internus can improve motor symptoms Parkinson's disease (PD). However, it is not known whether DBS can help reduce the signs and symptoms of the limb-kinetic, ideomotor or ideational apraxia associated with PD or if apraxia can exist as a stimulation induced side effect from DBS therapy. In this study, we look to conduct a pilot study to examine the feasibility of characterizing the prevalence of apraxia in PD patients with chronic, stable DBS.

Official Title

Apraxia in Parkinson's Disease Patients With Deep Brain Stimulation

Quick Facts

Study Start:2021-06-01
Study Completion:2024-01-28
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:TERMINATED

Study ID

NCT04725773

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 80 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Patients with PD as defined by the UK Brain Bank Criteria
  2. 2. Male or female, ages 18 to 80 years old
  3. 3. Chronically implanted DBS of either the STN or GPi for a minimum of 6 months
  1. 1. Other neurological diagnoses (e.g. Alzheimer's disease, atypical parkinsonism, stroke)
  2. 2. History of previous neurosurgical intervention that was not DBS
  3. 3. Patients with DBS of targets other than the STN or GPi, or leads in both targets
  4. 4. Patients in whom there is poor manual dexterity for a reason other than PD (e.g. orthopedic injury, amputation)
  5. 5. Patients with a diagnosis of PD dementia

Contacts and Locations

Principal Investigator

Bhavana Patel, DO
PRINCIPAL_INVESTIGATOR
University of Florida

Study Locations (Sites)

UF Health at the University of Florida
Gainesville, Florida, 32608
United States

Collaborators and Investigators

Sponsor: University of Florida

  • Bhavana Patel, DO, PRINCIPAL_INVESTIGATOR, University of Florida

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2021-06-01
Study Completion Date2024-01-28

Study Record Updates

Study Start Date2021-06-01
Study Completion Date2024-01-28

Terms related to this study

Additional Relevant MeSH Terms

  • Deep Brain Stimulation
  • Parkinson Disease
  • Apraxia, Motor