Validity and Reliability of Smartphone Use in Measuring Joint Position Sense in Patients With Knee Osteoarthritis

Aliaa Rehan Youssef

Status: Completed

Conditions: Knee Osteoarthritis

Treatments: Device: Smartphone application (Goniometer Pro )

Study type: Observational

Funder types: Other

Identifiers

NCT03658915

AY32

Details and patient eligibility

About

This study will investigate the concurrent validity and intra-rater reliability of using smartphone in assessing joint position sense in patient with knee osteoarthritis.

Full description

Knee osteoarthritis is the most common arthritis. Such disease is complicated by many musculoskeletal dysfunction such as disturbed joint position sense, which impairs their ability to perform their regular daily activities. As rehabilitation should target impairment in function, it is essential that therapists assess joint sense during baseline and follow-up evaluation of patients to decide on needed therapeutic interventions. Joint position sense can be assessed by various methods such as motion tracking systems and the isokinetic dynamometer, yet these equipment are expensive and are not readily available at regular clinical settings.

Smartphone has been introduced as an assessment tool in rehabilitation of musculoskeletal disorders. For the knee joint, smartphone has been validated for measuring range of motion and joint position sense in healthy population, yet it has never been validated in patients with knee osteoarthritis. Therefore, this study will investigate smartphone validity and reliability as an assessment tool of knee position sense in patients with knee osteoarthritis.

Enrollment: 33 patients

Sex: All

Ages: 40 to 60 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Patient must be referred to the outpatient clinic of the faculty of Physical Therapy and Medicine, Cairo University with a confirmed diagnosis of unilateral or bilateral osteoarthritis of the knee and having one or more of the following criteria (ASo, 2000).
• Morning stiffness for less than 30 minutes.
• Crepitus on active knee movement.
• Bony enlargement either palpable or visible in radiographs.
• Bony tenderness at joint margins.
• Age 40-60 years old.

Exclusion criteria

• Steroid injection within 2 months prior to inclusion.
• Presence of neurologic disorders (e.g., stroke, Parkinson's disease, or poliomyelitis). •Presence of other rheumatoid or orthopedic disorders in the lower extremity or spine. •A recent history of a lower extremity fracture with in the past year.
• History of ligament deficiency, such as anterior cruciate ligament or meniscal injury.
• Severe pain with active movement.
• Poor memory or cognitive function.

Trial design

33 participants in 2 patient groups

Osteoarthritis

Description:

Thirty symptomatic knee with osteoarthritis will be recruited according to the following criteria: INCLUSION CRITERIA: 1. Referred with a confirmed diagnosis of unilateral or bilateral OA of the knee based on the following criteria. 1.1. Morning stiffness \< 30 minutes, 1.2. Crepitus on active knee movement. 1.3. Bony enlargement either palpable or visible in radiographs. 1.4. Bony tenderness. 2. Age 40-60 years old. EXCLUSION CRITERIA: 1. Steroid injection within the past 2 months. 2. Presence of neurologic disorders. 3. Presence of of orthopedic diseases or trauma in the lower extremity or spine within the past year. 6. Severe pain with active movement 7. Poor memory or cognitive function

Treatment:

Device: Smartphone application (Goniometer Pro )

Control

Description:

Thirty asymptomatic knee will be recruited for this study. Control group participants will be age-matched to the osteoarthritis group, and should have no pain or other relevant clinical symptoms in lower quadrant.

Treatment:

Device: Smartphone application (Goniometer Pro )