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Active, not recruitingNCT07134452Updated Aug 21, 2025

Comparison of Strength, Weight Bearing, Proprioception, Reaction Time and Function in Scapholunate Instability

An observational study in Scapholunate Interosseous Ligament Injury, Scaphoid-Lunate Instability and Scapholunate Dissociation, sponsored by Hacettepe University. Active, not recruiting at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-08-21.

Sponsored by Hacettepe University · Observational

From the registry’s dates

  • Primary completion was expected by Oct 2025, 1 year ago, but the record still lists the study as active, not recruiting.
Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
40
Ages
18 Years to 45 Years
Sex
All
01

Study summary

Scapholunate (SL) instability is the most common type of instability seen in the wrist, resulting from SLI injury or excessive mobility [1,2]. It usually occurs after trauma and can range from mild injury to severe malalignment [3]. Symptoms include dorsal pain, clicking sound, limited movement, increased pain with weight-bearing, and weakness [4,5]. Pain reduces joint movement and grip strength, limiting daily activities [6]. If there is no dislocation, conservative treatment (education, exercise, splinting) is applied [7].

The wrist absorbs and transfers load through ligaments. During flexion-extension, the scaphoid and lunate follow the capitate [10]. SLIL injuries alter forearm muscle activation. EKRL, EKRB, APL, and FKR are "scapholunate-friendly" muscles; EKU is not recommended due to its pronator effect [12-15]. SLIL mechanoreceptors enhance dynamic stability [11,19]. There are no studies objectively measuring the strength of these muscles.

Isokinetic muscle assessment has not been performed in SL instability. These measurements objectively determine muscle strength and imbalances, personalizing treatment. Weight transfer capacity, reaction time, and proprioception have also not been studied. However, weight transfer is an indicator of stability, proprioception is critical for functionality, and reaction time reflects neuromuscular response speed [23-27].

The aim of this study is to compare forearm isokinetic muscle strength, grip strength, weight transfer, proprioception, reaction time, and functionality in individuals with SL instability with those in healthy individuals.

Read the detailed description

Scapholunate (SL) instability is the most common type of instability in the wrist, resulting from injury or excessive mobility of the scapholunate interosseous ligaments (SLIL) [1,2]. This condition, which typically arises following trauma, can range in severity from partial ligament injury to irreparable ligament damage and malalignment [3]. Symptoms include dorsal pain, clicking sounds, limited range of motion, a sensation of catching, pain exacerbated by loading, and weakness [4,5]. Pain that occurs during weight-bearing can reduce joint range of motion and grip strength, thereby limiting daily living activities [6]. In cases without radiological findings of dislocation, conservative treatment (education, exercise, splinting) is preferred [7].

The wrist facilitates load absorption and transfer through complex mechanisms and ligaments. During flexion and extension, the scaphoid and lunate follow the movement of the capitate [10]. In SLI injuries, impaired ligament-muscular reflexes alter the activation patterns of the forearm muscles. Among these muscles, the extensor carpi radialis longus (ECRL), extensor carpi radialis brevis (ECRB), abductor pollicis longus (APL), and flexor carpi radialis (FCR) are defined as scapholunate-friendly; the extensor carpi ulnaris (ECU) has been reported as a muscle to be avoided due to its intracarpal pronator effect [12-15].

In recent years, it has been emphasized that static stability approaches are insufficient and that neuromuscular control has gained importance [2]. It has been shown that the SLIL and wrist ligaments are rich in mechanoreceptors and that these structures increase dynamic stability by activating the forearm muscles [11,19]. However, there are no studies that objectively measure the strength of the scapholunate-friendly muscles.

There is no information in the literature regarding the evaluation of wrist muscles in SL instability using an isokinetic system. Isokinetic measurements are also extremely limited in other pathologies affecting the wrist [20-22]. Isokinetic devices measure muscle strength at a constant speed, objectively determining performance at different speeds and revealing muscle imbalances. This enables treatment plans to be personalized.

Similarly, there are no studies examining parameters such as weight transfer capacity, reaction time, and proprioception in SL instability. However, upper extremity load transfer is an important indicator of stability [23-25], and proprioception is critical for functionality. Reaction time indicates the neuromuscular system's ability to respond quickly, and it is thought that this mechanism may be affected in instability [26,27].

This study aims to investigate forearm isokinetic muscle strength, grip strength, weight transfer capacity, proprioceptive sensation, reaction time, and functionality in individuals with scapholunate instability compared to healthy individuals.

Hypotheses H1: Isokinetic forearm muscle strength in patients with SL instability differs from that in healthy individuals.

H2: Grip strength differs between patients with SL instability and healthy individuals.

H3: Proprioceptive sensation differs between patients with SL instability and healthy individuals.

H4: Reaction time differs between patients with SL instability and healthy individuals.

H5: Weight transfer onto the hand differs between patients with SL instability and healthy individuals.

H6: Upper extremity functionality differs between patients with SL instability and healthy individuals.

02

Conditions studied

  • Scapholunate Interosseous Ligament Injury
  • Scaphoid-Lunate Instability
  • Scapholunate Dissociation

Keywords

  • Scapholunate Instability
  • Isokinetic Muscle Strength
  • Weight Bearing
  • Proprioceptive Sensation
  • Reaction Time
  • Functionality
03

In context

Lead sponsor

Hacettepe University is the lead sponsor of 983 studies on the registry; 212 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Adults aged 18-45 years. The case group will include individuals diagnosed with scapholunate instability confirmed by clinical and radiological examination. The control group will consist of age- and sex-matched healthy individuals with no history of wrist injury or upper extremity musculoskeletal disorders.

Inclusion criteria

  • Being between the ages of 18-45
  • Applying to the clinic within the last 6 months
  • Being diagnosed with dynamic scapholunate instability

Exclusion criteria

Exclusion Criteria:

  • Having a history of previous hand or wrist surgery,
  • Having a history of Reflex Sympathetic Dystrophy,
  • Having a Scapholunate Advanced Collapse lesion,
  • Having a serious systemic neurological, or psychiatric illness,
  • Having been undergoing upper extremity rehabilitation in the last six months, did not wish to participate in the study, or were unable to follow the protocols.
05

Study design

Observational model
Case-control
Time perspective
Cross-sectional
Enrollment
40 participants (estimated)
Patient registry
No

Groups and cohorts

  • Scapholunate Instability Group

    Individuals diagnosed with scapholunate interosseous ligament injury confirmed by clinical and radiological assessment. Participants will undergo baseline evaluations including isokinetic muscle strength, grip strength, weight-bearing capacity, proprioception, reaction time, and functional assessments.

    Diagnostic Test: Baseline Assessments

  • Healty Controls

    Age- and sex-matched healthy individuals with no history of wrist injury or upper extremity musculoskeletal disorders. Participants will undergo the same baseline evaluations as the scapholunate instability group.

    Diagnostic Test: Baseline Assessments

Interventions

  • Diagnostic testBaseline Assessments

    Evaluation of isokinetic muscle strength, grip strength, upper extremity weight-bearing capacity, proprioceptive sense, reaction time, and functional performance in both groups

06

What researchers measure

Primary outcomes

  1. Isokinetic Muscle Strength Evaluation

    It will be evaluated with the Isokinetic Cybex device. At 60/90/ angular velocities, the extensor-flexor peak torque force / work produced by the muscle will be evaluated concentrically.

    Time frame: Baseline

  2. Weight-Bearing Test

    Test protocol: The subject will be asked to apply as much pressure as possible with the extended elbow and wrist on a digital scale. The subjects will perform 3 trials and the average value will be recorded in kilograms and will be compared with the weight transfer test of the unaffected hand, which is determined as a normative value for maximum weight-bearing capacity.

    Time frame: Baseline

  3. Grip Strength Evaluation

    It will be evaluated with the JAMAR hand held dynamometer

    Time frame: Baseline

  4. Wrist Proprioception Evaluation

    t will be evaluated with the Isokinetic Cybex Device device The hand will be brought to the target angle value of 30 degrees extension or 30 degrees flexion with the help of a physiotherapist and will be waited for approximately 5 seconds. After the patient learns, he/she will be asked to do it himself/herself with his/her eyes closed. After the movement is repeated 3 times in a row, the participant will be asked to actively apply the determined target extension movement to the same extremity. The difference between the target angle and the measured angle.The difference between the target angle and the measured angle will be recorded as the margin of error.

    Time frame: Baseline

  5. Reaction Time Evaluation

    Upper extremity reaction time evaluation will be performed with the reaction speed measurement and exercise set Blazepod Trainer (Blazepod Trainer Device, Play Coyotta Ltd. Tel Aviv Israel) device. Individuals will be asked to turn off the 5 LEDs placed on the table in front of them as quickly as possible with one hand in the sitting position. Both hands will be evaluated. The number of LEDs extinguished in 30 seconds (number), the unit extinguishing time (msec) and the number of LEDs missed when the LEDs extinguished after a 5-second waiting period will be recorded. Measurements will be made on both hands.

    Time frame: Baseline

  6. Pain Evaluation

    It contains 10 cm line that should be assigned according to perceived pain intensity at rest, during activity and while exercising.

    Time frame: Baseline

  7. Quick DASH

    The QuickDASH is a subset of 11 items from the 30-item DASH and is a self-reported questionnaire in which the response options are presented as 5-point Likert scales. At least 10 of the 11 items must be completed for a score to be calculated and the scores range from 0 (no disability) to 100 (most severe disability). This score was designed be useful in patients with any musculoskeletal disorder of the upper limb.

    Time frame: Baseline

Secondary outcomes

  1. PRWHE (Patient-Rated Wrist/Hand Evaluation)

    Patient-Rated Wrist/Hand Evaluation (PRWHE) is a self-reported questionnaire designed to assess wrist and hand pain and functional status. It consists of 15 items, including 5 pain-related questions and 10 function-related questions. Each item is scored on a 0-10 scale, with higher scores indicating greater pain or disability. The total score ranges from 0 (best) to 100 (worst).

    Time frame: Baseline

07

Study locations

1 site
  • Istanbul Yeni Yuzyil University
    Istanbul, Cevizlibag / Zeytinburnu 34010, Turkey (Türkiye)
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 21, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07134452
Lead sponsor
Hacettepe University
Collaborators
İstanbul Yeni Yüzyıl Üniversitesi
Responsible party
Arzu Dağ (Doctorate student, Hacettepe University) — Principal investigator
First posted
Aug 21, 2025
Start date
Jun 1, 2025
Primary completion
Oct 1, 2025 (estimated)
Completion
Dec 1, 2025 (estimated)
Last update
Aug 21, 2025

Study contacts

Arzu Dağ
principal investigator · Hacettepe University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is active, not recruiting, as verified in Aug 2025. You cannot join it, but the record below documents what was studied.

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