- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05837247
Effects of Telemonitoring-supported Game-based Home Exercises in Juvenile Idiopathic Arthritis
Effects of Telemonitoring-supported Game-based Home Exercises on Kinesiophobia, Pain and Quality of Life in Juvenile Idiopathic Arthritis
In order to cope with pain, improve quality of life and prevent kinesiophobia in children with juvenile idiopathic arthritis, most of the physiotherapy approaches used so far are standard.
However, nowadays, it has been observed that participation in treatment has increased with game-based exercises instead of standard physiotherapy. In addition, remote monitoring applications made it possible to perform physiotherapy programs, which are an integral part of the treatment in children with JIA, who is difficult to reach the clinic due to reasons such school schedule and living area, through remote monitoring. This project aimed to investigate the effects of telemonitoring-supported game-based home exercise programs on pain, kinesiophobia and quality of life.
The original aspect of our project is to include telemonitoring-supported game-based home exercise programs as an alternative physiotherapy program in children with JIA. Its contribution to clinical practice is to change the perspective of physiotherapists and children on standard physiotherapy practices, to increase their motivation, and to ensure children's participation in treatment.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Juvenile rheumatic diseases are chronic diseases with a prognosis ranging from complete recovery to long-term disability. Juvenile idiopathic arthritis (JIA) is the most common rheumatologic disease in children. Pain is one of the main clinical symptoms in JIA. Due to pain, these children with rheumatic diseases avoid moving. The fear of moving because of this pain is defined as kinesiophobia. Kinesiophobia (fear of movement); It is defined as an excessive and unreasonable fear of physical action to avoid harm or re-injury. Its prevalence in chronic pain varies between 50-70%. Regular physical activity and fitness exercises can prevent kinesiophobia; Treatment includes therapeutic exercises and cognitive behavioral therapy.
In order to cope with pain, improve quality of life and prevent kinesiophobia in children with juvenile idiopathic arthritis, most of the physiotherapy approaches used so far are standard.
However, nowadays, it has been observed that participation in treatment has increased with game-based exercises instead of standard physiotherapy. In addition, remote monitoring applications made it possible to perform physiotherapy programs, which are an integral part of the treatment in children with JIA, who is difficult to reach the clinic due to reasons such school schedule and living area, through remote monitoring. This project aimed to investigate the effects of telemonitoring-supported game-based home exercise programs on pain, kinesiophobia and quality of life.
In this study, the participants will be evaluated and training game-based exercises at the baseline examination. Then, the participants will be followed the online synchronous communication application-based telemonitoring method After the game-based home exercises intervention, the participants will be re-evaluated again and the results will be compared.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Istanbul, Turkey, 34000
- Istanbul University-Cerrahpasa
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Whose are diagnosed with JIA at least 1 year ago
- Whose are aged 6-16 years
- Whose are having pain in lower extremity joints for more than the last 6 months
- Whose have stable medical treatment
- Whose are at a level to understand the games and perform the activities mentally
Exclusion Criteria:
- Patients with neurological problems in addition to rheumatic diagnosis
- Individuals who are contraindicated to exercise
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
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Experimental: Game-based telerehabilitation exercises
The telemonitoring-supported program will be conducted with a smartphone application synchronously.
The participants will be monitored by the investigators using an online communication application during exercise sessions.
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online Game-based home exercises are physiotherapy programs that include exercises transformed into game activities to increase the child's participation in the rehabilitation process.
The exercises were planned such as; the dwarf camel game as squat exercises; the flamingo balance game as single leg balance exercises and weight-bearing activities etc.
The exercise program will be conducted for 6 weeks and 3 sessions in a week.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The Wong-Baker Faces Pain Rating Scale
Time Frame: immediately After intervention
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A self-report tool called The Wong-Baker Faces Pain Rating Scale is used to assess how much pain kids are experiencing. It is widely acknowledged that measuring children's pain is challenging for medical professionals. This is because children express pain differently than adults due to differences in their language, communication, and developmental stages. The Wong-Baker Pain Scale has 6 faces. The first face represents a pain score of 0 and indicates "not hurt". The second face is a 2 represents the pain score and means "it hurts a little". The third face represents a pain score of 4 and "it hurts a little more" shows. The fourth face represents a pain score of 6 and indicates "it hurts more". The fifth face represents a pain score of 8. and shows that "it hurts a lot"; the sixth face represents a pain score of 10 and indicates "worst pain". The unit of this outcome is a score. |
immediately After intervention
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Pediatric Quality of Life Inventory (PedsQL) 3.0 Arthritis Module
Time Frame: immediately After intervention
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Patients with JIA have the Pediatric Quality of Life Inventory (PedsQL) 3.0 arthritis module.
This criterion has been translated into Turkish and its validity has been demonstrated.
44 Evaluations are made about pain and suffering (four questions), daily activities (five questions), treatment (seven questions), anxiety (three questions), communication (three questions), and parent and child modules are evaluated separately.
The unit of this outcome is a score.
Every item is 5-point Likert scale type.
Scores are transformed on a scale from 0 to 100.
Items are reverse scored and linearly transformed to a 0-100 scale as follows: 0=100, 1=75, 2=50, 3=25, 4=0.
Higher scores mean better quality of life and fewer problems or symptoms
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immediately After intervention
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The Tampa Scale for Kinesiophobia
Time Frame: immediately After intervention
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It is a 17-item scale developed to measure the fear of movement/re-injury.
The scale includes parameters of injury/re-injury and fear-avoidance in work-related activities.
A 4-point Likert scoring (1 = I strongly disagree, 4 = I totally agree) is used in the scale.
After reversing items 4, 8, 12 and 16, a total score is calculated.
The person gets a total score between 17-68.
A high score on the scale indicates a high level of kinesiophobia.
It is recommended to use the total score in studies.
In our study, the fear of avoiding movement will be evaluated with TSK.
The unit of this outcome is a score.
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immediately After intervention
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Hip flexion-extension range of motion
Time Frame: immediately After intervention
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The pre-study and post-study hip flexion/extension passive ranges of motion (ROM) were measured by goniometric measurement.
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immediately After intervention
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Hip internal-external rotation range of motion
Time Frame: immediately After intervention
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The pre-study and post-study hip internal-external rotation passive ranges of motion (ROM) were measured by goniometric measurement.
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immediately After intervention
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Hip abduction/adduction range of motion
Time Frame: immediately After intervention
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The pre-study and post-study hip abduction/adduction passive ranges of motion (ROM) were measured by goniometric measurement.
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immediately After intervention
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Knee flexion and extension range of motion
Time Frame: immediately After intervention
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The pre-study and post-study knee flexion and extension passive ranges of motion (ROM) were measured by goniometric measurement.
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immediately After intervention
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Ankle dorsi-plantar flexion range of motion
Time Frame: immediately After intervention
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The pre-study and post-study ankle dorsi-plantar flexion passive ranges of motion (ROM) were measured by goniometric measurement.
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immediately After intervention
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
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10 meter walk test
Time Frame: immediately After intervention
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It is widely used and recommended as a measure of gait speed.
It can be employed to determine functional mobility, gait.
The unit of this outcome is second.
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immediately After intervention
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Gait speed
Time Frame: immediately After intervention
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When assessing many aspects of a patient's functional mobility, practitioners find gait speed to be a very useful statistic.
Moreover, gait speed is frequently employed as a predictor of general health and function due to its capacity to be altered by a number of body systems.
The data will be collected from video recordings that asked participants to walk at a 10-meter walkway and videos will be analyzed with Kinovea 2D movement analysis.
The unit of this outcome is meter/second.
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immediately After intervention
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Collaborators and Investigators
Investigators
- Study Chair: Gökçe Leblebici, Phd, Pt, İstanbul medeniyet University
Publications and helpful links
General Publications
- Arman N, Tarakci E, Tarakci D, Kasapcopur O. Effects of Video Games-Based Task-Oriented Activity Training (Xbox 360 Kinect) on Activity Performance and Participation in Patients With Juvenile Idiopathic Arthritis: A Randomized Clinical Trial. Am J Phys Med Rehabil. 2019 Mar;98(3):174-181. doi: 10.1097/PHM.0000000000001001.
- Crayne CB, Beukelman T. Juvenile Idiopathic Arthritis: Oligoarthritis and Polyarthritis. Pediatr Clin North Am. 2018 Aug;65(4):657-674. doi: 10.1016/j.pcl.2018.03.005.
- Minden K, Niewerth M. [Juvenile idiopathic arthritis--clinical subgroups and classification]. Z Rheumatol. 2008 Mar;67(2):100, 102-6, 108-10. doi: 10.1007/s00393-007-0246-5. German.
- Weermeijer JD, Meulders A. Clinimetrics: Tampa Scale for Kinesiophobia. J Physiother. 2018 Apr;64(2):126. doi: 10.1016/j.jphys.2018.01.001. Epub 2018 Mar 19. No abstract available.
- Zaripova LN, Midgley A, Christmas SE, Beresford MW, Baildam EM, Oldershaw RA. Juvenile idiopathic arthritis: from aetiopathogenesis to therapeutic approaches. Pediatr Rheumatol Online J. 2021 Aug 23;19(1):135. doi: 10.1186/s12969-021-00629-8.
- Grassini S. Virtual Reality Assisted Non-Pharmacological Treatments in Chronic Pain Management: A Systematic Review and Quantitative Meta-Analysis. Int J Environ Res Public Health. 2022 Mar 29;19(7):4071. doi: 10.3390/ijerph19074071.
- Hadjiat Y, Marchand S. Virtual Reality and the Mediation of Acute and Chronic Pain in Adult and Pediatric Populations: Research Developments. Front Pain Res (Lausanne). 2022 May 6;3:840921. doi: 10.3389/fpain.2022.840921. eCollection 2022.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- IstanbulUC_ccrpts
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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