Proprioception and Meditation

August 2, 2019 updated by: Joseph Signorile, University of Miami

The Effects of Yoga Based Meditation on Proprioception in Individuals With Parkinson's Disease

In past work is has been shown that yoga can be as effective as a standard balance or Tai Chi protocol; however, there is an inability to distinguish between the mind and body contributions of yoga training. This study will compare an accepted proprioceptive training program to a meditation program which concentrates on body awareness in individuals with Parkinson's disease.

Study Overview

Study Type

Interventional

Enrollment (Actual)

20

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Florida
      • Coral Gables, Florida, United States, 33147
        • Laboratory of Neruomuscular Research and Active Aging

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.

Eligibility Criteria

Ages Eligible for Study

40 years to 90 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • An individual must be between 40 and 90 years of age with mild to moderate Parkinson's Disease (Hoehn & Yahr stages I-III).

Exclusion Criteria:

  • Participants that have been part of a formal training program that targeted lower body strength, balance or proprioception within the past six months
  • Participants that have any uncontrolled nerve (except Parkinson's patients taking appropriate medication), bone or joint, or heart disease;
  • Participants that have been advised by a doctor to not exercise;
  • Participants that have regularly practiced yoga at least twice per week within the past six months;
  • Participants that is unable to consent;
  • Participants that is a prisoner;
  • Participants that are pregnant.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Proprioceptive Drills
Includes drills during which participants perform multiplestances on a pillow, a number of different cone and line drills, reaching drills, object retrieval drills and drills using balls to disturb balance.
Active balance and proprioception drills
Experimental: Yoga Meditation
The meditation program will use simple poses during which the participant will not move and will concentrate on each of the participant's body parts and where they are in space.
Yoga meditation using motor imagery to perceive movement patterns

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Joint Position Sense
Time Frame: 20 minutes
The joint position sense technique for the knee involves the reduction of visual cues while moving the knee to a specific target angle, holding that target angle, returning the knee to the starting position, and then reproducing that target angle.
20 minutes
Tinetti balance and gait.
Time Frame: 3 minutes.
A subjective evaluation of Balance and gait.
3 minutes.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
8ft Up and Go
Time Frame: 60 seconds
Individuals sits in a chair at the verbal cue of "go", individual rises from chair and walks as quickly as possible around a cone placed 8 ft from the front of the chair, individual returns to and sits.
60 seconds
Joint Kinesthesia
Time Frame: 20 minutes
The Joint Kinesthesia measurement technique involves the participant sitting in the Biodex chair with visual, audio, and tactile cues reduced and the leg supported by an external movement device. The knee is placed at a predetermined angle and slowly flexed or extended at a random starting time while the participant is instructed to signal when movement is felt.
20 minutes
Dynamic Posturography
Time Frame: 5 minutes
The participant stands on a randomly moving platform with a sonar emitter affixed to the lumbar spine. As the platform moves the linear and curvilinear displacement of the emitter is evaluated and a dynamic movement analysis core is generated.
5 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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 Major Dates

Study Start (Actual)

January 17, 2017

Primary Completion (Actual)

March 30, 2018

Study Completion (Actual)

July 30, 2019

Study Registration Dates

First Submitted

March 8, 2017

First Submitted That Met QC Criteria

March 8, 2017

First Posted (Actual)

March 15, 2017

Study Record Updates

Last Update Posted (Actual)

August 6, 2019

Last Update Submitted That Met QC Criteria

August 2, 2019

Last Verified

August 1, 2019

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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