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Completed

NCT Number: NCT03658915

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

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

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Key information

Age range

40 year–60 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Faculty of Physical Therapy, Cairo University

Dokki, Egypt

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Smartphone application (Goniometer Pro )

Device

Knee repositioning error will be measured simultaneously by smartphone and Biodex isokinetic dynamometer by a single blind assessor. All assessments will be done with eyes closed and repeated over two separate sessions, with one-week interval in-between. For active repositioning, the participant will actively extend the knee to reach a predetermined target position45° flexion at an angular velocity of 10°/sec. For passive knee repositioning, the isokinetic dynamometer will move the knee at 5°/s to a predetermined angle between 5° and 80° of flexion and the participant should stop the movement when the predetermined angle is reached.

Primary outcomes

  1. concurrent validity of smartphone against isokinetic dynamometry in measuring joint position sense.

    Time frame: One day

    The extent to which a measure by Goniometer Pro application related to an outcome which is joint position sense in isokinetic dynamometer

Secondary outcomes

  1. Intrarater reliability of smartphone measurements

    Time frame: 1 week

    same investigator will repeat joint position sens assessment using smartphone application

Sponsors and collaborators

Lead sponsor

Aliaa Rehan Youssef

Other

Registry information

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Sep 6, 2018
Registry last updated
Feb 5, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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