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The Effects of Dual Task Training in Individuals With Parkinson's Disease

Not Applicable
Completed
Conditions
Parkinson's Disease
Interventions
Behavioral: Dual Task Group
Behavioral: Single Task Group
Registration Number
NCT02538029
Lead Sponsor
The Cleveland Clinic
Brief Summary

The primary aim of the proposed project is to characterize dual tasking (DT) deficits to improve motor, cognitive, and quality of life outcomes in individuals with Parkinson's disease (PD). Phase 1 of the intervention will involve an in-depth gait analysis on 15 individuals with PD. This gait analysis will utilize the Computer Assisted Rehabilitation Environment (CAREN) system, a virtual reality system with a fully integrated 3-D motion capture system. The purpose of Phase 1 is to generalize characteristics of gait and postural control during specific DT conditions. Phase 2 (N=20) involves the clinical translation of these findings. This phase will involve creating a clinical intervention based on the objective information gathered the CAREN system. The intervention will take place 3x/week for a total of 8 weeks. Interventional groups will include: 1) DT clinical group (N=10) and 2) Single task group (N=10). Outcome measures will be used at the beginning and end of the intervention to assess the feasibility and efficacy of the intervention.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
45
Inclusion Criteria
  • Clinical diagnosis of idiopathic PD
  • Able to provide informed consent
  • Ability to ambulate ≥ 300ft with or without an assistive device
  • Hoehn and Yahr stage 2-4
Exclusion Criteria
  • Undergone any surgical procedure for the treatment of PD, such as deep brain stimulation
  • Those who are considered to be high risk exercisers per American College of Sports Medicine exercise screening questionnaire
  • Musculoskeletal injury or neurological injury other than PD that would restrict physical activity
  • Inability to follow 2 step commands
  • Significant cognitive impairment as designated by ≥ 3 errors on the Short Portable Mental Status Questionnaire

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Dual Task GroupDual Task GroupThis group will complete an exercise intervention that involves performing dual tasking activities (simultaneously performing 2 things at once). This group will exercise 3x/wk for 8 weeks.
Single Task GroupSingle Task GroupThis group will complete an exercise intervention that involves performing single task activities. The participant will perform motor tasks and cognitive tasks individually. This group will exercise 3x/wk for 8 weeks.
Primary Outcome Measures
NameTimeMethod
Walking Speed During GaitPhase 1: baseline; Phase 2: baseline, end of treatment (8 weeks), and end of treatment +4 weeks

Average self-selected walking speed without dual tasking.

Step Length During GaitPhase 1: baseline; Phase 2: baseline, end of treatment (8 weeks), and end of treatment +4 weeks

The average distance from heel strike of the less affected leg to heel strike of the more affected leg. Higher values indicate a longer step length.

Secondary Outcome Measures
NameTimeMethod
2 Minute Walk TestPhase 1: baseline; Phase 2: baseline, end of treatment (8 weeks), and end of treatment +4 weeks

A functional endurance assessment, reporting total distance traveled over a 2 minute period. Higher values indicate better functional endurance.

Trail Making TestPhase 2: baseline, end of treatment (8 weeks), and end of treatment +4 weeks

Cognitive task where the participant connects 25 dots in numerical order. Lower scores indicate better cognitive function. Reported here is total time to complete the task.

Quality of Life in Neurological Disorders QuestionnairePhase 2: baseline, end of treatment (8 weeks), and end of treatment +4 weeks

Quality of life questionnaire. Reported here is T-Score for the Lower Extremity domain. A T-score of 50 is the mean of the reference population, with higher scores indicating a better outcome.

Activities-specific Balance Confidence ScalePhase 2: baseline, end of treatment (8 weeks), and end of treatment +4 weeks

Balance questionnaire. Scores range from 0-100, with higher scores indicating greater balance confidence.

Reaction TimePhase 2: baseline, end of treatment (8 weeks), and end of treatment +4 weeks

Average time taken to react to a choice of two stimuli. Lower scores indicate better reaction time.

Trial Locations

Locations (1)

Cleveland Clinic

🇺🇸

Cleveland, Ohio, United States

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