Mobile App Use for Physical Activity in Knee Osteoarthritis
NCT ID: NCT06721208
Last Updated: 2025-02-10
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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NOT_YET_RECRUITING
NA
150 participants
INTERVENTIONAL
2025-05-02
2026-12-02
Brief Summary
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"What physical activity can I perform with knee osteoarthritis?" Researchers will compare use of app developed to provide physicial activity program versus educational advices (a look-alike substance that contains no drug) to see if APP works to treat pain and stiffness related to knee osteoarthritis.
Participants will:
Download and use APP Visit the clinic once every 4 weeks for checkups and tests
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Detailed Description
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* patients who will use the "Move for Knee" APP (intervention arm);
* patients who will be advised to engage in free physical activity (control arm). Patients will be directed to one of the arms through random sampling with consecutive 1:1 randomization (intervention:control).
The mobile APP called Move Your Knee is divided in 4 sections:
1. Know Your Knee: this first section allows the collection of data entered by patients, useful for understanding their lifestyle habits and daily physical activity level, and information relating to KOA pathology.
At the end of the questionnaire, the algorithm integrated into the APP's computer code will allow the calculation of the patient's presumed level of physical activity. This will then be followed by the assignment of a specific form which includes the exercises and the related execution parameters (i.e. weekly frequency), and useful advice for safely carrying out the exercises to achieve the specific functional objectives.
2. Move Your Knee: in this section, the patient will be able to select the level of difficulty/intensity in performing the physical exercise (the more advanced levels are blocked until the previous objective is achieved).
There are 5 levels, each marked by an evocative image that summarizes the functional meaning and, therefore, facilitates the identification of the type of user (in particular, from the most advanced level: "Hawk"; "Tiger"; "Bull", "Turtle", "Sloth").
Once the exercise program has been started, the patient finds the indications/advice for carrying out each exercise (duration, series and repetitions). Through the motion capture function, he can record the exercise he performed, to check with your doctor the appropriateness and safety of its execution. The video obtained from this recording is saved in the APP's Database (DB) and can be transferred to the doctor via Chat.
3. Step by step: through this section, patients have the opportunity to record and monitor daily progress, obtaining a real-time view of their progress.
4. Chat: to facilitate direct contact with the doctor, the APP is equipped with a native instant messaging service, through which patients can directly contact their doctor by communicating and sharing files and videos useful for monitoring.
The system is completed with a control panel that is used by the doctor via terminal/PC. This tool allows:
1. registration of the patient on a specific web platform;
2. access to the patient files associated with the referring doctor;
3. patient monitoring, viewing the patient's progress to monitor adherence to use;
4. access to Chat. Patients will be visited at baseline corresponding to enrollment in the study (T0), and at 30 (T1), 90 (T2), and 180 days (T3).
At all time points patients will be evaluated with the following protocol:
* multidimensional pain evaluation with
* the Brief Pain Inventory (BPI) and its two indexes (severity and interference indexes; BPI-SI, BPI-II);
* the Leeds Assessment of Neuropathic Symptoms and Signs (LANSS) scale, for the neuropathic component of pain;
* stiffness and function through Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC);
* quality of life through EUROQoL-5Dimension (EQ-5D). For patients in the intervention group, questions related to the "user experience" and any adverse effects related to the APP will be included through an open-ended question "describe your experience with the APP" at 30 (T1), 90 (T2), and 180 days (T3).
Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
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intervention
\- patients who will use the "Move for Knee" APP (intervention arm);
use the "Move for Knee" APP
The mobile APP called Move Your Knee allows the collection of data entered by patients, useful for understanding their lifestyle habits and daily physical activity level, and information relating to KOA pathology.
At the end of the questionnaire, the algorithm integrated into the APP's computer code will allow the calculation of the patient's presumed level of physical activity. This will then be followed by the assignment of a specific form which includes the exercises and the related execution parameters (i.e. weekly frequency), and useful advice for safely carrying out the exercises to achieve the specific functional objectives.
control
patients who will be advised to engage in free physical activity (control arm).
No interventions assigned to this group
Interventions
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use the "Move for Knee" APP
The mobile APP called Move Your Knee allows the collection of data entered by patients, useful for understanding their lifestyle habits and daily physical activity level, and information relating to KOA pathology.
At the end of the questionnaire, the algorithm integrated into the APP's computer code will allow the calculation of the patient's presumed level of physical activity. This will then be followed by the assignment of a specific form which includes the exercises and the related execution parameters (i.e. weekly frequency), and useful advice for safely carrying out the exercises to achieve the specific functional objectives.
Eligibility Criteria
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Inclusion Criteria
* Expression of consent to participate in the study through a signed informed consent form
* Ability to understand and use the APP through a practical demonstration in an outpatient setting
Exclusion Criteria
* Pregnancy or breastfeeding
45 Years
70 Years
ALL
Yes
Sponsors
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University of Campania Luigi Vanvitelli
OTHER
Responsible Party
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Sara Liguori
doctor
Central Contacts
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References
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Li E, Tan J, Xu K, Pan Y, Xu P. Global burden and socioeconomic impact of knee osteoarthritis: a comprehensive analysis. Front Med (Lausanne). 2024 May 16;11:1323091. doi: 10.3389/fmed.2024.1323091. eCollection 2024.
Iolascon G, Migliore A, Beretta G, Bernetti A, Bortolotti R, Celano A, Giarratano A, Marinangeli F, Momoli A, Sebastiani GD, Tomasini A, Tonolo S, Madotto F, Di Martino A, Natoli S. Pain Management in Knee Osteoarthritis: Insights from an Exploratory Online Survey of Italian Patients and Physicians. Healthcare (Basel). 2024 Oct 18;12(20):2077. doi: 10.3390/healthcare12202077.
Geng R, Li J, Yu C, Zhang C, Chen F, Chen J, Ni H, Wang J, Kang K, Wei Z, Xu Y, Jin T. Knee osteoarthritis: Current status and research progress in treatment (Review). Exp Ther Med. 2023 Aug 25;26(4):481. doi: 10.3892/etm.2023.12180. eCollection 2023 Oct.
Lee J, Chang RW, Ehrlich-Jones L, Kwoh CK, Nevitt M, Semanik PA, Sharma L, Sohn MW, Song J, Dunlop DD. Sedentary behavior and physical function: objective evidence from the Osteoarthritis Initiative. Arthritis Care Res (Hoboken). 2015 Mar;67(3):366-73. doi: 10.1002/acr.22432.
Zmerly H, Milanese C, El Ghoch M, Itani L, Tannir H, Kreidieh D, Yumuk V, Pellegrini M. Personalized Physical Activity Programs for the Management of Knee Osteoarthritis in Individuals with Obesity: A Patient-Centered Approach. Diseases. 2023 Dec 14;11(4):182. doi: 10.3390/diseases11040182.
Scopaz KA, Piva SR, Wisniewski S, Fitzgerald GK. Relationships of fear, anxiety, and depression with physical function in patients with knee osteoarthritis. Arch Phys Med Rehabil. 2009 Nov;90(11):1866-73. doi: 10.1016/j.apmr.2009.06.012.
Other Identifiers
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0008758/i-21/03/2024
Identifier Type: -
Identifier Source: org_study_id
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