The Effects of Tele-Rehabilitation-Based Dual-Task Upper Extremity Training in Patients With Parkinson's Disease

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age40+
SponsorSaglik Bilimleri Universitesi

About this trial

The aim of this study is to compare the effects of tele-rehabilitation-based synchronous and asynchronous dual-task upper extremity training with clinical based dual-task upper extremity training and conventional single-task upper extremity training in patients with Parkinson's disease. The main questions it aims to answer are:

* Whether there are differences in motor symptoms, hand dexterity, upper extremity functions, grip strength, executive functions, daily living activities, and treatment satisfaction between tele-rehabilitation-based synchronous and asynchronous dual-task upper extremity training, clinical-based dual-task upper extremity training, and conventional single-task upper extremity training in patients with Parkinson's disease. * Whether there is a difference in telemedicine satisfaction between tele-rehabilitation-based synchronous and asynchronous dual-task upper extremity training in patients with Parkinson's disease.

Researchers will compare conventional single-task upper extremity training, clinical-based dual-task upper extremity training, tele-rehabilitation-based synchronous upper extremity training and tele-rehabilitation-based asynchronous upper extremity training.

Participants will:

* Receive upper extremity exercise training at the study clinic or home, twice a week for approximately 60 minutes each time, for 6 weeks. * Participate in assessments at the study clinic before and after exercise training.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Having been diagnosed with Parkinson's disease by a neurologist according to the UK Brain Bank criteria

Being in stage 3 or higher according to the Hoehn-Yahr Scale

Having a caregiver capable of providing the necessary assistance during tele-rehabilitation sessions and using the required equipment and programs.

Having the device and software to conduct remote video calls for tele-rehabilitation

Disqualifiers

Presence of a neurological disease other than Parkinson's disease

Cognitive impairment (Standardized Mini Mental Test score less than 24)

Having undergone deep brain stimulation surgery

Having a visual, auditory, or perceptual problem

Trial design

Design model

Parallel

Treatments tested in this trial

  • Conventional Single Task Upper Extremity Exercise Training

    Other intervention

    Conventional single task upper extremity exercise training at clinical setting. The first 5 minutes of the training session will consist of a warm-up period of stretching and breathing exercises, followed by a cool-down period of the same exercises.Nine different upper extremity activities (using a fork and spoon, tying shoelaces, reaching, throwing a ball, filling water, folding a sheet, drawing shapes, buttoning, and fastening nuts) will be performed for 3 minutes each, in a random order. A 2-minute rest period will be given between each activity.

  • Clinic-Based Dual Task Upper Extremity Exercise Training

    Other intervention

    Dual task upper extremity exercise training at clinical setting. The first 5 minutes of the training session will consist of a warm-up period of stretching and breathing exercises, followed by a cool-down period of the same exercises.Nine different upper extremity activities (using a fork and spoon, tying shoelaces, reaching, throwing a ball, filling water, folding a sheet, drawing shapes, buttoning, and fastening nuts) will be performed simultaneously with three randomly selected cognitive tasks (arithmetic task, verbal fluency, digit span) for 3 minutes each, in a random order. A 2-minute rest period will be given between each activity.

  • Tele-Rehabilitation Based Synchronous Dual Task Upper Extremity Exercise Training

    Other intervention

    Dual task upper extremity exercise training at patient's home, synchronous with a researcher via tele-rehabilitation method. The first 5 minutes of the training session will consist of a warm-up period of stretching and breathing exercises, followed by a cool-down period of the same exercises.Nine different upper extremity activities (using a fork and spoon, tying shoelaces, reaching, throwing a ball, filling water, folding a sheet, drawing shapes, buttoning, and fastening nuts) will be performed simultaneously with three randomly selected cognitive tasks (arithmetic task, verbal fluency, digit span) for 3 minutes each, in a random order. A 2-minute rest period will be given between each activity.

  • Tele-Rehabilitation Based Asynchronous Dual Task Upper Extremity Exercise Training

    Other intervention

    Dual task upper extremity exercise training at patient's home, asynchronous under a researcher supervision. It will be carried out according to the pre-determined schedule and will be video recorded. The first 5 minutes of the training session will consist of a warm-up period of stretching and breathing exercises, followed by a cool-down period of the same exercises.Nine different upper extremity activities (using a fork and spoon, tying shoelaces, reaching, throwing a ball, filling water, folding a sheet, drawing shapes, buttoning, and fastening nuts) will be performed simultaneously with three randomly selected cognitive tasks (arithmetic task, verbal fluency, digit span) for 3 minutes each, in a random order. A 2-minute rest period will be given between each activity.

Treatment groups

40 Participants
are divided into 4 treatment groups
Group A: Single Task TrainingActive comparator 1 intervention
Group B: Clinic-Based Dual Task TrainingExperimental treatment 1 intervention
Group C: Tele-Rehabilitation Based Synchronous Dual Task TrainingExperimental treatment 1 intervention
Group D: Tele-Rehabilitation Based Asynchronous Dual Task TrainingExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Unified Parkinson's Disease Rating Scale (UPDRS) - PART 3

UPDRS is a reliable and valid scale that assesses cognitive skills, mood, daily living activities, motor skills, motor fluctuations, dyskinesias and autonomic dysfunction and is widely used in clinical studies and research in Parkinson's disease. The motor symptoms section, which is the third section of this scale, will be used.

Time frame
From enrollment to the end of training at 6 weeks
2

Hoehn & Yahr Scale

It is a staging system that provides information quickly in determining the severity and symptoms of Parkinson's disease.

Time frame
From enrollment to the end of treatment at 6 weeks
3

Nine-Hole Peg Test

During the test, individuals use only one hand to pick up nine wooden pegs one by one and insert them into the holes as quickly as possible. After inserting all the pegs, they quickly place them back into the container one by one. The timer starts when the individual touches the first peg and ends when the last peg is placed back into the container.

Time frame
From enrollment to the end of treatment at 6 weeks
4

Coin Rotation Test

This test assesses the coordination of independent finger movements. In this test, the person is asked to rotate a coin 180 degrees as many times as possible between their thumb, index finger, and middle finger within 10 seconds without dropping it. The person's performance is video recorded and later analyzed. An increase in the number of times the patient rotates the coin within 10 seconds indicates better fine motor skills.

Time frame
From enrollment to the end of treatment at 6 weeks

Secondary outcomes

1

Treatment Satisfaction

Patient satisfaction with treatment will be assessed post-treatment using a 100 mm long visual-analog scale.

Time frame
At end of treatment at 6 weeks
2

Telemedicine Satisfaction Questionnaire

This survey consists of 14 items. It assesses patients' satisfaction levels with the software or system they use for treatment or other remote rehabilitation services. The total score ranges from 14 to 70, with a maximum of 5 points per question. A higher score indicates higher satisfaction.

Time frame
At end of treatment at 6 weeks

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Saglik Bilimleri Universitesi

Lead sponsor

Anadolu University

Collaborator

Eskisehir Osmangazi University

Collaborator