CClinicalTrials.gg
CompletedNCT06232850Updated Jul 6, 2026

Wrist Position Sense in Individuals With Multiple Sclerosis

An observational study in Multiple Sclerosis, sponsored by Pamukkale University. Completed at 1 site in Turkey (Türkiye). Open to participants aged 18 Years to 50 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-07-06.

Sponsored by Pamukkale University · Observational

Study type
Observational
Model
Case-control
Time perspective
Cross-sectional
Enrollment
48
Ages
18 Years to 50 Years
Sex
All
01

Study summary

No study has been found examining the effect of wrist position sense on manual dexterity in individuals with multiple sclerosis.The purpose of this study is to examine the effect of wrist position sense on manual dexterity of the hand.

Read the detailed description

Multiple sclerosis is a chronic demyelinating disease of the central nervous system that occurs in young adults and usually progresses with attacks and remissions. As the disease progresses, symptoms such as fatigue, muscle weakness, loss of balance, loss of sensation, spasticity, visual disturbances and bladder dysfunction are observed. In addition to these symptoms, hand functions may be affected even in the early stages of the disease.

Appropriate motor control and mobility skills are required to perform manual dexterity effectively. Joint stabilization and perception of the joint's position and movement in space are needed for motor control of hand functions. In this process, position sense signals contribute significantly to the target localization and performance of the hand. Position sense signals must be constantly updated for the coordination and integration of hand position during manual activities such as holding or grasping an object. This is possible with a healthy sense of position.

Although it is known that position sense is affected in MS patients, no study has been found examining the effect of wrist position sense on manual dexterity. The purpose of this study is to examine the effect of wrist position sense on hand dexterity. Patients' manual dexterity will be evaluated using the Purdue Pegboard Test, and wrist position sense will be evaluated using the K-FORCE Sens® electrogoniometer.

02

Conditions studied

  • Multiple Sclerosis

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Keywords

  • Multiple Sclerosis
  • Manual Dexterity
  • Position Sense
03

In context

Multiple Sclerosis

3,460 studies on the registry are indexed under Multiple Sclerosis; 661 are open to participants now.

This study's enrollment of 48 is below the median of 100 across 1,016 observational studies indexed under Multiple Sclerosis.

Browse Multiple Sclerosis studies →

Lead sponsor

Pamukkale University is the lead sponsor of 331 studies on the registry; 61 are open to participants now.

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

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Who can participate

Ages eligible
18 Years to 50 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

MS and healthy individuals who proper the inclusion and exclusion criteria

Inclusion criteria

  • Patient group:

    • Disability score (EDSS: Expanded Disability Status Scale) should be between 0-3.
    • Being between the ages of 18-50
    • Not having had an attack in the last 3 months
    • Scoring 24 points or above on the Mini-Mental State Examination
    • Patients diagnosed with relapsing-remitting MS with a disease duration of at least 2 years
    • Patients without spasticity according to MAS

Control group:

  • Volunteers in a similar age range who agreed to participate in the study
  • Being between the ages of 18-50

Exclusion criteria

Exclusion Criteria:

  • Patient group:

    • Presence of diagnosed visual impairment
    • Having other chronic diseases not related to MS
    • Having any orthopedic, neurological, rheumatological or metabolic diagnosis that causes upper extremity involvement
    • History of hand and upper extremity disorders, peripheral nerve disorders, and medical or psychiatric disorders that may significantly affect cognitive function
    • Presence of wrist joint range of motion limitation

Control group:

  • Having any orthopedic, neurological, rheumatological or metabolic diagnosis that causes upper extremity involvement
  • History of hand and upper extremity disorders, peripheral nerve disorders, and medical or psychiatric disorders that may significantly affect cognitive function
  • Presence of wrist joint range of motion limitation
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Study design

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

Groups and cohorts

  • Multiple sclerosis patient

    According to EDSS should be between 0-3, not having had an attack in the last 3 months and without spasticity according to MAS in patient with MS will assesment KFORCE Sens® device and Purdue Pegboard Test.

    Other: Position sense and manual dexterity evaluate

  • Healthy group

    Healthy people of similar age who agree to participate in the study will evaluate the KFORCE Sens® device and the Purdue Pegboard Test.

    Other: Position sense and manual dexterity evaluate

Interventions

  • OtherPosition sense and manual dexterity evaluate

    Position sense and manual dexterity evaluate

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What researchers measure

Primary outcomes

  1. Wrist Position Sense Assessment

    Wrist position sense will be assessed with the KFORCE Sens® electrogoniometer. Target measurement values of 30° for wrist flexion, 30° for extension, 10° for radial deviation and 15° for ulnar deviation will be used.

    Time frame: four mounth

Secondary outcomes

  1. Purdue Pegboard Test (PPT)

    PPT evaluates the gross motor skills of the arm, hand and fingers, as well as the fine motor skills of the fingers and fingertips, both unilaterally and bilaterally. It consists of pins, washers, nuts and assembly tests. The test consists of 5 sub-steps (inserting pins with the dominant/non-dominant hand/both hands, mathematical summation and assembly). The scoring of the test is the total number of pins, washers and nuts installed at the end of the given period. One trial will be made for each subtest.

    Time frame: four mounth

07

Study locations

1 site
  • Müge içelli güneş
    Denizli, Deni̇zli̇ 20160, Turkey (Türkiye)
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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 Jul 6, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06232850
Lead sponsor
Pamukkale University
Responsible party
müge içelli (lecturer, Pamukkale University) — Principal investigator
First posted
Jan 31, 2024
Start date
Jan 11, 2024
Primary completion
Apr 1, 2024
Completion
Apr 1, 2024
Last update
Jul 6, 2026

Study contacts

Müge İçelli Güneş, M.Sc.
principal investigator · Pamukkale University Denizli Health Services Vocational School of Higher Education

Oversight

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

Not currently enrolling

This study is completed, as verified in Jul 2026. You cannot join it, but the record below documents what was studied.

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