Efficiency of Supervised Exercise Program Versus Mobile-Based Exercise Program in Juvenile Idiopathic Arthritis
NCT ID: NCT06193681
Last Updated: 2025-09-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
54 participants
INTERVENTIONAL
2024-03-20
2025-09-10
Brief Summary
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Physical, individual, social and psychological factors that create barriers to PA and exercise participation in children and adolescents with rheumatic disease significantly affect PA and exercise adherence. In this regard, online applications stand out as an important strategy for encouraging behavioral change, providing motivational and social support, and allowing feedback and interaction with health professionals using information and communication technologies.
It is emphasized that digital health applications should be designed more comprehensively and personalized to increase participation in PA promotion and regular exercise programs and be compared with control group exercise programs in order to increase their usability in this disease population and examine their effectiveness.
This study will be planned as a randomized controlled study. Adolescent JIA patients between the ages of 12-18 will be included in the study and will be divided into 2 groups. The first group will receive a personalized exercise program under the supervision of a physiotherapist, 3 sessions per week (2 session face to face, 1 session online) for 12 weeks. A personalized mobile application-based exercise program will be applied to the second group for the same week and frequency. This study can contribute to the literature by investigating effective methods in improving physical fitness, physical activity, walking and balance functions in patients with JIA.
Adolescents in both groups will be given smart watches to promote PA and monitor health parameters. The evaluation periods for both groups are stated below; T0: Start T1: Before the exercise program (after 3 months of PA monitoring with a smart watch) T2: It will be carried out after the exercise program (12 weeks later). The effectiveness of the exercise program to be applied on the evaluation parameters will be demonstrated by comparing the two groups after the exercise program.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Pedi@ctivity Exercise Mobile Application
Pedi@ctivity Exercise Mobile Application Exercise Program
The first group of the study received a mobile application (Pedi@ctivity) based exercise program. With the Pedi@ctivity exercise mobile application, the selected exercises and exercise program will be offered personalized to each adolescent for 12 weeks. After 12 weeks, the effectiveness of the Pedi@ctivity mobile application-based exercise program on the evaluation parameters will be investigated.
Supervised Exercise Group
Supervised Exercise Group
In the physiotherapist-supervised personalized exercise program, the exercises selected through the Pedi@ctivity exercise mobile application will be applied to adolescents under the supervision of a physiotherapist (2 sessions face-to-face, 1 session online/synchronous).
Interventions
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Pedi@ctivity Exercise Mobile Application Exercise Program
The first group of the study received a mobile application (Pedi@ctivity) based exercise program. With the Pedi@ctivity exercise mobile application, the selected exercises and exercise program will be offered personalized to each adolescent for 12 weeks. After 12 weeks, the effectiveness of the Pedi@ctivity mobile application-based exercise program on the evaluation parameters will be investigated.
Supervised Exercise Group
In the physiotherapist-supervised personalized exercise program, the exercises selected through the Pedi@ctivity exercise mobile application will be applied to adolescents under the supervision of a physiotherapist (2 sessions face-to-face, 1 session online/synchronous).
Eligibility Criteria
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Inclusion Criteria
* Being diagnosed with JIA at least 6 months ago at the Istanbul Medical Faculty Pediatric Rheumatology Clinic
* Being diagnosed with Oligoarticular/Polyarticular JIA
* Volunteering to participate in the study
Exclusion Criteria
* Having an additional chronic disease affecting the musculoskeletal system
* Having vision or hearing problems
* Having a level of cognitive impairment that cannot understand the commands given
12 Years
18 Years
ALL
No
Sponsors
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Istanbul University - Cerrahpasa
OTHER
Responsible Party
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Ayse Asena Yekdaneh
Principal Investigator
Principal Investigators
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Nilay Arman, Assoc. Prof.
Role: STUDY_CHAIR
Istanbul University-Cerrahpaşa, Faculty of Health Science, Department of Physiotherapy and Rehabilitation
Nuray Aktay Ayaz, Prof. Dr.
Role: STUDY_CHAIR
Istanbul Faculty of Medicine, Department of Internal Medicine, Department of Pediatric Rheumatology
Asena Yekdaneh
Role: PRINCIPAL_INVESTIGATOR
Istanbul University-Cerrahpasa, Institute of Postgraduate Education
Locations
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Istanbul University-Cerrahpasa, Institute of Postgraduate Education
Istanbul, , Turkey (Türkiye)
Countries
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Other Identifiers
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AAYekdaneh1
Identifier Type: -
Identifier Source: org_study_id
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