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Video Exercise Mobile Application for People With Knee Osteoarthritis

Development and Investigation of the Effectiveness of Video Exercise Mobile Application for People With Knee Osteoarthritis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06422910
Enrollment
52
Registered
2024-05-21
Start date
2023-05-02
Completion date
2024-05-15
Last updated
2024-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteoarthritis, Knee, Telerehabilitation

Brief summary

The aim of our study is to realize an exercise training and follow-up system that individuals with knee OA can easily adapt.

Interventions

OTHERTelerehabilitation

Home exercises will be delivered through a video mobile application. In this application, exercises for knee osteoarthritis will be presented according to their types (stretching, strengthening, etc.). Videos deemed appropriate by the physiotherapist will be added to the exercise prescription and sent to the patients via message. Patients will have the opportunity to remotely access their own exercise prescription with visual, auditory and written commands. Translated with DeepL.com (free version)

Sponsors

The Scientific and Technological Research Council of Turkey
CollaboratorOTHER
Fatih Ozden
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosis of primary knee osteoarthritis (OA) according to the American College of Rheumatology (ACR) criteria * Be qualified to use the mobile application and agree to use the application

Exclusion criteria

* Individuals with poor cognitive function or inadequate reading skills * Individuals with neurological disorders that may affect mobility skills * Individuals who have undergone knee joint surgery and individuals with traumatic injuries

Design outcomes

Primary

MeasureTime frameDescription
Visual Analog Scale (VAS)Change from Baseline VAS at 8 weeksOn a 0 cm straight line or numeric scale, the patient is asked to mark the pain they feel (0: no pain, 10: excruciating pain).
The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)Change from Baseline WOMAC at 8 weeksWOMAC consists of 3 main headings: pain intensity, stiffness and physical function. The total score ranges from 0 (no disability) to 96 (complete disability).
Satisfaction and expectation assessmentChange from Baseline Satisfaction and expectation assessment at 8 weeksOn a 0 cm straight line or numeric scale, the patient will be asked to mark their pre-treatment expectation and post-treatment satisfaction level. 0 will represent the lowest expectation and satisfaction and 10 the highest expectation or satisfaction.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026