Development and Application of Tele-Neuro Rehabilitation System

Development and Application of Tele-Neuro Rehabilitation System: An Example of Digital Transformation in Health

Disability due to neurological diseases is increasing in our country and world. With regular physiotherapy and rehabilitation, as well as patients' symptoms are brought under control, their affected functions in daily life are achieved and levels of independence and physical activity increase. Thus, the patients' quality of life and participation in social life is improved and patients are supported in physical, social and psychological terms. In recent years, it has been reported that exercise with telerehabilitation systems increase the compliance and participation of patients to the treatment, and even this system seems as effective as standard rehabilitation practices. Delivering the treatment through telerehabilitation system when that patients cannot receive it in the hospital due to epidemic, restriction, transfer difficulties, personal and environmental limitations will enable patients to receive the rehabilitation services.Telerehabilitation system is frequently encountered in the abroad, but there are limited systems with Turkish version specific to this patient group in our country. The aim of project is to develop and detect the efficiency of a telerehabilitation system which is used to assess, follow and design home-based rehabilitation program among individuals with chronic neurological diseases who have difficulty in participating in physiotherapy and rehabilitation services because of personal or environmental reasons.

Study Overview

• Status: Recruiting
• Conditions: Stroke; Multiple Sclerosis; Parkinson Disease
• Intervention / Treatment: Other: Telerehabilitaton; Other: Home Exercise

Detailed Description

The coding and design of this telerehabilitation system will enable easy access to all devices via the website. The expert interface of the system will consist of three interfaces; exercise videos to be prepared by physiotherapists will be uploaded, patient list and feedback of patients. Rehabilitation programs can be prepared and updated. There will be a panel in the patient interface that will allow the patient to access a rehabilitation program tailored to the problem and to communicate about the ongoing program when needed. In the manager interface, high-level control of many steps such as adding experts from different institutions, organizing information, creating an exercise pool will be provided. With the project, a telerehabilitation system will be put into practice, where patients can easily access the rehabilitation services from their homes, and patients can contact with clinicians when they need follow-up and treatment.

The patients and their caregivers will be informed about the system and project. In the assessment part, the physical performance will be determined. Also, questionnaires such as fall efficacy or activities of daily living will be requested through the system. Thus, a detailed assessment of the patient will be completed to reveal the problems. A rehabilitation program with appropriate exercises will be defined for patients in the telerehabilitation group and patients will be asked to apply this program three days a week for eight weeks. Patients in the control group will be placed on the waiting list after the first evaluations and no additional treatment will be applied by asking them to maintain their routine activity levels within this period. At the end of eight weeks, initial evaluations will be repeated in two groups.

This user-friendly telerehabilitation system with turkish language support will be the first comprehensive system that will let to assess, give exercise programs and follow the progression in patients with chronic neurologic disorders. With this system, the opportunity to reach more patients in the home environment will be provided. Rehabilitation programs will promote the physical capacity, health-related quality of life and it will also cause reducing in the burden of caregivers. After evaluating the applicability of our program, we will pave the way for the introduction of telerehabilitation care in health institutions and in areas with transportation issues, furthermore low-cost, sustainable system will be achieved to our country.

• Study Type: Interventional
• Enrollment (Anticipated): 114
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: Yonca Zenginler Yazgan, Asst. Prof.; Phone Number: +905344245350; Email: yoncazenginler@gmail.com

Study Locations

• Turkey
  • Istanbul, Turkey
    • Recruiting
    • Istanbul University-Cerrahpasa
    • Contact: Yonca Zenginler Yazgan; Email: yoncazenginler@gmail.com

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 25 years to 65 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Chronic patients diagnosed with neurological disease at least 1 year ago by a neurologist
• Multiple sclerosis patients with an Expanded Disability Status Scale (EDSS) score of ≤6, who are in the stable phase of the disease and have not had an attack in the last 3 months
• Parkinson's patients with a Hoehn and Yahr score ≤3
• Stroke patients with a modified Rankin score of ≤3
• To have an internet infrastructure where the system can be accessed at home
• Not participating in a standardized physiotherapy and rehabilitation program within the last 3 months
• Having a companion with the patient during the exercises

Exclusion Criteria:

• Presence of blurred or poor vision problems
• Hearing and speech impairment at a level that will affect participation in the system
• Epilepsy
• The presence of pregnancy
• Having any cognitive problems that prevent using the system
• History of trauma / fracture in the last 3-6 months
• Having pacemaker
• Presence of cardiac problems
• Presence of serious respiratory diseases

Study Plan

How is the study designed?

Design Details

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

Number of Arms

6

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Stroke (Telerehabilitation); Exercise therapy with telerehabilitation system	Other: Telerehabilitaton; Patients will be asked to apply the rehabilitation program defined for them 3 days a week for 8 weeks. A training session will last approximately 45-60 minutes.
Other: Stroke (Home Exercise); Exercise therapy with brochure	Other: Home Exercise; Patients will be asked to apply the rehabilitation program for themselves with an exercise brochure. This therapy will last 3 days a week for 8 weeks.
Experimental: Multiple Sclerosis (Telerehabilitation); Exercise therapy with telerehabilitation system	Other: Telerehabilitaton; Patients will be asked to apply the rehabilitation program defined for them 3 days a week for 8 weeks. A training session will last approximately 45-60 minutes.
Other: Multiple Sclerosis (Home Exercise); Exercise therapy with brochure	Other: Home Exercise; Patients will be asked to apply the rehabilitation program for themselves with an exercise brochure. This therapy will last 3 days a week for 8 weeks.
Experimental: Parkinson Disease (Telerehabilitation); Exercise therapy with telerehabilitation system	Other: Telerehabilitaton; Patients will be asked to apply the rehabilitation program defined for them 3 days a week for 8 weeks. A training session will last approximately 45-60 minutes.
Other: Parkinson Disease (Home Exercise); Exercise therapy with brochure	Other: Home Exercise; Patients will be asked to apply the rehabilitation program for themselves with an exercise brochure. This therapy will last 3 days a week for 8 weeks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Independent Standing Test (The change between the initial value and the value after 2 months will be evaluated).	It tests the patient's ability to stand for 20 seconds in an upright position without any support or assistance, with her/his feet shoulder-width apart and arms free at the side of the body.	Baseline and end of weeks 8.
Romberg Test (The change between the initial value and the value after 2 months will be evaluated).	The patient is asked to stand in an upright position with his feet open at shoulder level, arms free at the side of the body, with eyes open and then closed, without losing his balance for 10 seconds before receiving any support. In case of excessive release or failure to continue the test, it is considered a Romberg positive or abnormal Romberg sign. It evaluates the effect of the patient's balance in the closed position.	Baseline and end of weeks 8.
One-Legged Standing Test (The change between the initial value and the value after 2 months will be evaluated).	It is a functional evaluation test that measures the patient's one-leg standing balance. The patient is asked to raise one leg in the air and keep the knee bent at hip level for at least 10 seconds. Times less than 10 seconds indicate a balance disorder, and times less than 5 seconds indicate a risk of falling. It is applied with the patient's eyes open and closed.	Baseline and end of weeks 8.
5 Times Sit and Stand Test (The change between the initial value and the value after 2 months will be evaluated).	It is a test that evaluates functional lower extremity strength, transfer, balance and fall risk. The time for the patient to sit and stand up from the chair 5 times is recorded. It has been proven to be valid in patients with stroke, Parkinson's and Multiple Sclerosis.	Baseline and end of weeks 8.
KATZ Independence Index in Activities of Daily Living (The change between the initial value and the value after 2 months will be evaluated).	It is a scale that measures the ability of the patient to do daily living activities independently and evaluates the functional status. It examines patient performances in six functions such as bathing, dressing, toilet, transfer, personal care and feeding. Patients score their activity independence in each of the six functions as 1 (independent) or 0 (dependent). A total score of 0 to 2 indicates severe dysfunction, a total score of 2 to 4 indicates moderate dysfunction, and a total score of 4 to 6 indicates full function.	Baseline and end of weeks 8.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Modified Fall Efficiency Scale (The change between the initial value and the value after 2 months will be evaluated).	It is a 14-item scale that measures the patient's confidence in falling. Each question is scored between 1-4. High scores indicate high fall anxiety.	Baseline and end of weeks 8.
World Health Organization Quality of Life Scale Short Form Turkish Version (WHOQOL-BREF-TR) (The change between the initial value and the value after 2 months will be evaluated).	It is a health-related quality of life scale developed by the World Health Organization. A national question was added to the Turkish version of the scale in addition to the original version. The scale measures physical, mental, social and environmental well-being and consists of a total of 27 questions with an additional question. Since each domain independently expresses the quality of life in its own field, field scores are calculated between 4-20. The higher the total score, the higher the quality of life.	Baseline and end of weeks 8.
Fatigue Severity Scale (The change between the initial value and the value after 2 months will be evaluated).	It is a scale that evaluates the severity of fatigue with 9 items that patients can answer on their own. Each item is scored between 1 (strongly disagree) and 7 (strongly agree). The total score is calculated by taking the average of 9 items. A high score indicates increased fatigue severity.	Baseline and end of weeks 8.
System Usability Scale (The change between the initial value and the value after 2 months will be evaluated).	It is a scale consisting of 10 questions widely used in the literature to evaluate the perceptibility and usability of interactive systems. It is scored from 1 (strongly disagree) to 5 (strongly agree). A high total score indicates that the system is detectable and usable.	Baseline and end of weeks 8.
Global Change Scale (The change between the initial value and the value after 2 months will be evaluated).	It is a scale that evaluates how much a person's current situation has changed compared to his previous state. The person is asked to choose an exchange score from -5 (much worse than my previous state) to +5 (much better than my previous state).	Baseline and end of weeks 8.

Collaborators and Investigators

• Sponsor: Istanbul University - Cerrahpasa (IUC)
• Collaborators: The Scientific and Technological Research Council of Turkey
• Investigators: Study Chair: Ela Tarakcı, Prof., Istanbul University-Cerrahpaşa Faculty of Health Sciences; Study Chair: Burcu Ersöz Hüseyinsinoğlu, Assoc. Prof, Istanbul University-Cerrahpaşa Faculty of Health Sciences; Study Chair: Murat Kürtüncü, MD, Istanbul University-Capa Faculty of Medicine, Department of Neurology; Study Chair: Muhammed Erdem İsenkul, Asst. Prof., Istanbul University-Cerrahpaşa Faculty of Engineering; Study Chair: Pelin Vural, Istanbul University-Cerrahpasa Institute of Postgraduate Education; Study Chair: Recep Örmen, Istanbul University-Cerrahpasa Institute of Postgraduate Education

Study record dates

Study Major Dates

• Study Start (Actual): April 1, 2021
• Primary Completion (Anticipated): September 1, 2022
• Study Completion (Anticipated): October 1, 2022

Study Registration Dates

• First Submitted: July 5, 2021
• First Submitted That Met QC Criteria: August 26, 2021
• First Posted (Actual): September 1, 2021

Study Record Updates

• Last Update Posted (Actual): September 1, 2021
• Last Update Submitted That Met QC Criteria: August 26, 2021
• Last Verified: July 1, 2021

More Information

Terms related to this study

• Keywords: Multiple Sclerosis; Stroke; Parkinson's Disease; Neurorehabilitation; Stroke Rehabilitation; E-Health; Neurologic Rehabilitation; Web Based Systems; Physical Therapy and Rehabilitation; Data Storage
• Additional Relevant MeSH Terms: Pathologic Processes; Brain Diseases; Central Nervous System Diseases; Nervous System Diseases; Immune System Diseases; Demyelinating Autoimmune Diseases, CNS; Autoimmune Diseases of the Nervous System; Demyelinating Diseases; Autoimmune Diseases; Parkinsonian Disorders; Basal Ganglia Diseases; Movement Disorders; Synucleinopathies; Neurodegenerative Diseases; Multiple Sclerosis; Sclerosis; Parkinson Disease
• Other Study ID Numbers: 120S843

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No