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Knee OsteoarthritisNCT07386977

Knee Joint Position Sense in Knee Osteoarthritis

An observational study of Knee Osteoarthritis and Gonarthrosis, run by Lokman Hekim University at 1 site in Turkey (Türkiye).

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record
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Trial summary

The aim of this study was to compare knee joint position sense between sitting with visual input and prone without visual input in individuals with knee osteoarthritis. Read more about this study

Who is it for?
Ages 40 to 80 years
Conditions the study is for
Knee Osteoarthritis, Gonarthrosis
How many people
58 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Mar 2025to 30 Dec 2026
Phase
Observational
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 40 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Participants diagnosed with knee osteoarthritis according to Kellgren-Lawrence grades 1-3 were included in the study.

Who may be able to join

  • Age between 40 and 80 years,
  • A confirmed diagnosis of knee osteoarthritis,
  • Absence of any health condition that could interfere with the measurement procedures.

Who cannot join

  • Refusal to participate in the study,
  • Presence of a diagnosed neurological disorder that could affect the measurements,
  • Presence of cardiopulmonary instability that could influence the measurements,
  • History of knee-related trauma within the past year,
  • Receipt of physiotherapy or rehabilitation treatment within the past year,
  • History of knee-related surgery,
  • Inability to follow verbal instructions due to insufficient cognitive function.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Lokman Hekim University

    Ankara

Other trials in Turkey (Türkiye)

About this study

Official title: Knee Joint Position Sense Under Different Testing Conditions in Individuals With Knee Osteoarthritis

The aim of this study was to compare knee joint position sense between sitting with visual input and prone without visual input in individuals with knee osteoarthritis.

Read the detailed description

Knee proprioception plays a critical role in joint stability, movement control, and the accurate perception and reproduction of joint position. In individuals with knee osteoarthritis (OA), alterations in joint structures, mechanoreceptor function, pain, and sensorimotor control may compromise joint position sense and increase errors during active joint position reproduction. However, proprioceptive performance is not solely determined by disease-related changes and may also be influenced by the conditions under which proprioception is assessed.

Both visual input and body position may influence proprioceptive performance. Visual information can provide additional sensory cues that support joint position estimation, whereas the absence of visual information may increase reliance on somatosensory and proprioceptive afferent input. Body position may also modify proprioceptive performance by altering gravitational demands, muscle activation patterns, joint loading, and sensory information arising from muscles and periarticular structures. Therefore, differences in joint position reproduction between testing conditions may reflect the combined influence of visual and positional factors rather than the isolated contribution of either factor.

Despite the clinical relevance of knee joint position sense, it remains unclear whether proprioceptive performance obtained under different visual and positional testing conditions is comparable and whether the response to these conditions differs between individuals with and without knee OA. Examining these condition-dependent differences may contribute to a better understanding of how proprioceptive assessment protocols influence measured joint position sense and may facilitate the interpretation and standardization of proprioceptive assessments.

Accordingly, the primary aim of this study was to compare absolute angular error during active knee joint position reproduction from 90° to 30° of knee flexion between individuals with and without knee OA under two different testing conditions: sitting with visual input and prone without visual input. A secondary aim was to investigate whether age and pain intensity were associated with proprioceptive error in individuals with knee OA.

Keywords
knee osteoarthritis, proprioception, angular error, joint position sense, gonarthrosis
Medical subject headings
Osteoarthritis, Knee

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07386977
Study groupRoleWhat they receive
Knee Osteoarthritis GroupParticipants diagnosed with knee osteoarthritis.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Proprioception Measurement

    During the measurement, the inclinometer was positioned over the proximal one-third of the fibula, with its axis aligned with the knee joint line, and secured using a strap. Measurements were performed in both the prone and sitting positions. Participants were instructed to actively move their knee from 90° of flexion toward the target position of 30° of flexion. Upon reaching the perceived target position, participants maintained the position for 5 seconds before returning to the starting position. Each measurement was repeated three times, with a 1-minute rest interval between trials. A 2-minute rest period was provided between the two testing positions to allow participants to change position and rest.

    Measured: through study completion, an average of 2 year

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Feb 2026
  2. Study start1 Mar 2025
  3. Primary completion30 Sep 2026 (estimated)
  4. Study completion30 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Other
Time perspective
Prospective
Enrolment
58 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07386977
Sponsor's protocol ID
LHU-FTR-ZSBD-04
Status last verified
Oct 2026
First submitted
28 Jan 2026
Last updated
7 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: We are planning not to share this data not to declare the data of our participants with any third group.

Questions about this trial

What is this clinical trial studying?

An observational study of Knee Osteoarthritis and Gonarthrosis, run by Lokman Hekim University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: under way, not looking for participants, as of the sponsor's last update on 7 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Proprioception Measurement (time frame: through study completion, an average of 2 year). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 7 Oct 2026.

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