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The Effectiveness of Telerehabilitation in Improving Upper Extremity in Parkinson's Patients

Not Applicable
Completed
Conditions
Parkinson Disease
Interventions
Other: Exercise
Registration Number
NCT04835649
Lead Sponsor
Gazi University
Brief Summary

Parkinson's Disease (PD) is a disease that affects the functional skills of the upper extremity with clinical findings such as bradykinesia, rigidity, and hypokinesia and causes limitations in the daily life activities of the patients. Task-oriented training (TOT) is a highly individualized, client-centered, occupational therapy, functional-based intervention compatible with motor learning and motor control principles such as intensive motor training, variable practice, and intermittent feedback. Few studies have been found on the TOT of the upper extremity in PD. Telerehabilitation of Parkinson's patients shows many strengths, such as cost-related and time-dependent ease, and the possibility of telecommunication with clinicians. In addition, the refinement of digital health solutions with the goal to offer a patient-tailored intervention remains an ongoing process. There are a limited number of studies on TOT and telerehabilitation of the upper extremity in PD. In addition, no studies have been found applying TOT through telerehabilitation. For this purpose, a study including TOT-based telerehabilitation in upper extremity education in PD was planned.

Detailed Description

This study is a randomized controlled study. The patients will be randomly divided into two groups as exercise and control. Balance and walking exercises consisting of 3 days a week for 6 weeks will be given to both groups as a home program. In addition, the exercise group will receive TOT-based telerehabilitation via video conferencing 3 days a week for 6 weeks. TOT will be formed from daily life activities such as reaching out, grasping, writing, and manual skills, which are frequently used in daily life. As the outcome measures, disease severity and disability, finger and hand function, hand strength, and quality of life will be evaluated.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
30
Inclusion Criteria
  • 45- 70 years of age
  • Having diagnosed with "Parkinson's Disease" by a specialist physician
  • Having between 1-3 stages according to the Hoehn and Yahr Scale
  • Mini-Mental Test score more than or equal 24
Exclusion Criteria
  • Any orthopedic, vision, hearing, cardiovascular, or perception problems that may affect the research results

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Control groupExerciseThe control group only will be given a home program that includes walking and balance exercises
Exercise groupExerciseThe group that will receive task-oriented training via telerehabilitation
Primary Outcome Measures
NameTimeMethod
Manual dexterity performance - Post interventionAssessment will be conducted immediately after the intervention

Nine Hole Peg test (9-HPT)

Finger and hand function - Post interventionAssessment will be conducted immediately after the intervention

Jebsen-Taylor Hand Function Test (JTHFT)

Manual dexterity performance - BaselineAssessment will be conducted before the intervention

Nine Hole Peg test (9-HPT)

Finger and hand function - BaselineAssessment will be conducted before the intervention

Jebsen-Taylor Hand Function Test (JTHFT)

Upper extremity performance (coordination, dexterity and functioning) - BaselineAssessment will be conducted before the intervention

Action Research Arm Test (ARAT)

Upper extremity performance (coordination, dexterity and functioning) - Post interventionAssessment will be conducted immediately after the intervention

Action Research Arm Test (ARAT)

Secondary Outcome Measures
NameTimeMethod
Isometric hand strength - BaselineAssessment will be conducted before the intervention

J-Tech ™

Disease severity and disability - Post interventionAssessment will be conducted immediately after the intervention

MDS-Unified Parkinson's Disease Rating Scale (MDS-UPDRS). The MDS-UPDRS has a maximum score of 272 and is composed of four parts: Part I (non-motor experiences of daily living), Part II (motor experiences of daily living), Part III (motor examination) and Part IV (motor complications) (UPDRS). (0= best , 272= worst)

Disease severity and disability - BaselineAssessment will be conducted before the intervention

MDS-Unified Parkinson's Disease Rating Scale (MDS-UPDRS). The MDS-UPDRS has a maximum score of 272 and is composed of four parts: Part I (non-motor experiences of daily living), Part II (motor experiences of daily living), Part III (motor examination) and Part IV (motor complications) (UPDRS). (0= best , 272= worst)

Isometric hand strength - Post interventionAssessment will be conducted immediately after the intervention

J-Tech ™

Isometric pinch strength - BaselineAssessment will be conducted before the intervention

Baseline® pinch meter

Isometric pinch strength - Post interventionAssessment will be conducted immediately after the intervention

Baseline® pinch meter

Health-related Quality of Life - BaselineAssessment will be conducted before the intervention

Parkinson's Disease Questionnaire 8 (PDQ-8). There are 8 questions in total and each question is scored from 0-4 points. High score indicates decreased quality of life

Health-related Quality of Life - Post interventionAssessment will be conducted immediately after the intervention

Parkinson's Disease Questionnaire 8 (PDQ-8). There are 8 questions in total and each question is scored from 0-4 points. High score indicates decreased quality of life

Trial Locations

Locations (1)

Gazi University, Faculty of Health Sciences, Department of Physiotherapy and Rehabilitation

🇹🇷

Ankara, Turkey

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