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Multiple SclerosisNCT07151534

Body Awareness, Trunk Stability, and Arm Function in MS

An observational study of Multiple Sclerosis, run by Hacettepe University at 1 site in Turkey (Türkiye).

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record
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Trial summary

The aim of this study is to investigate the relationship between body awareness, trunk stabilization, and upper extremity functionality in patients with Multiple Sclerosis (MS). Hypotheses of the study: H1: There is a significant relationship between body awareness and upper extremity functionality in patients with… Read more about this study

Who is it for?
Ages 10 years and olderHealthy volunteers can take part
Conditions the study is for
Multiple Sclerosis
How many people
50 participants
Where
1 siteTurkey (Türkiye)
Study dates
6 Aug 2025to 1 Jan 2027
How long will I take part?
1 Day
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 10 years and older
  • All sexes
  • Healthy volunteers accepted
  • Child, Adult, Older adult

Study population: MS patients and healthy subjects with inclusion criteria

Who may be able to join

  • Diagnosed with Multiple Sclerosis (MS) by a neurologist according to the McDonald criteria
  • Aged 18 years or older
  • Expanded Disability Status Scale (EDSS) score ≤ 5
  • Mini-Mental State Examination (MMSE) score ≥ 24
  • A control group consisting of healthy individuals matched with MS patients in terms of age and sex

Who cannot join

  • Having a neurological disorder other than MS
  • Having experienced a relapse and/or used corticosteroids in the past 3 months
  • Having an orthopedic/systemic condition affecting the upper extremities or trunk
  • Being pregnant
  • Refusing to participate or not providing written informed consent
  • Healthy individuals who have an orthopedic/systemic condition affecting the upper extremities or trunk, who are pregnant, or who do not agree to participate and provide written informed consent will be excluded.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Güngör Beyza Özvar Şenöz contact

5053888617 ext. +90

beyzaozvar@gmail.com

Turkey (Türkiye)1 site, 1 recruiting
  • Hacettepe University

    Ankara, Altındağ

    Güngör Beyza Özvar Şenöz, PhD, 5053888617 ext. +90, beyzaozvar@gmail.com

    Recruiting

Other trials in Turkey (Türkiye)

About this study

Official title: Investigation of the Relationship Between Body Awareness, Trunk Stabilization, and Upper Extremity Functionality in Individuals With Multiple Sclerosis

The aim of this study is to investigate the relationship between body awareness, trunk stabilization, and upper extremity functionality in patients with Multiple Sclerosis (MS).

Hypotheses of the study:

H1: There is a significant relationship between body awareness and upper extremity functionality in patients with MS.

H2: There is a significant relationship between body awareness and trunk stabilization in patients with MS.

H3: Body awareness is reduced in patients with MS compared to healthy individuals.

H4: Trunk stabilization is reduced in patients with MS compared to healthy individuals.

H5: Upper extremity functionality is reduced in patients with MS compared to healthy individuals.

Read the detailed description

Patients' demographic and disease-specific information will be recorded. Subsequently, body awareness, upper extremity functionality, and trunk stabilization will be assessed.

Keywords
body awareness, upper extremity, trunk stabilization, multiple sclerosis
Medical subject headings
Multiple Sclerosis

What participants receive

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

Study groups in NCT07151534
Study groupRoleWhat they receive
Multiple SclerosisDiagnosed with Multiple Sclerosis (MS) by a neurologist according to the McDonald criteria, aged 18 years or older, Expanded Disability Status Scale (EDSS) score of ≤ 5, Mini-Mental State Examination score of 24 or higher will be included in the study.
HealthyA control group consisting of healthy individuals matched with MS patients by age and sex will be included in the study.

What is being measured

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

  1. Body Awareness Questionnaire

    To assess body awareness, the Body Awareness Questionnaire will be used.This questionnaire consists of 18 items, each scored on a scale from 1 to 7, and evaluates body awareness. Higher scores indicate better body awareness. The Turkish version has been validated and found to be reliable.

    Measured: up to 6 months

  2. Body Awareness Rating Questionnaire

    To assess body awareness,the Body Awareness Rating Questionnaire will be used. Body Awareness Rating Questionnaire:This questionnaire includes 24 items across 4 domains: function, mood, feeling/sensation, and awareness. Higher scores indicate better body awareness. The Turkish version has been validated and shown to be reliable.

    Measured: up to 6 months

  3. Upper Extremity Functionality-Grip strength

    Grip strength will be measured with a Jamar dynamometer. It will be performed three times bilaterally, and average values (kg) will be recorded.

    Measured: up to 6 months

  4. Upper Extremity Functionality-Pinch strength

    Pinch strengths will be assessed using a Baseline pinch gauge. It will be performed three times bilaterally, and average values (kg) will be recorded.

    Measured: up to 6 months

  5. Upper Extremity Functionality-Nine Hole Peg Test (9HPT)

    The 9HPT will evaluate hand dexterity by timing how quickly participants place and remove nine pegs. Each hand will be tested three times. It will be recorded in seconds. An average time ≥33.3 seconds will indicate dysfunction in MS patients.

    Measured: up to 6 months

  6. Trunk Stabilization- Trunk Impairment Scale (TIS),

    Trunk stabilization will be evaluated using the TIS.TIS: Assesses static/dynamic balance and trunk coordination (17 items, 0-23 points).

    Measured: up to 6 months

  7. Trunk Stabilization-plank endurance test

    Trunk stabilization will be evaluated using the plank endurance test. The test measures core endurance. Plank test: Time held in forearm plank recorded. It will be recorded in seconds.

    Measured: up to 6 months

  8. Trunk Stabilization-side bridge test

    Trunk stabilization will be evaluated using the side bridge test. The test measures core endurance Time held in side plank on both sides recorded.It will be recorded in seconds.

    Measured: up to 6 months

  9. Trunk Stabilization-Modified Biering-Sorensen

    Trunk stabilization will be evaluated using the Modified Biering-Sorensen test. The test measures core endurance. Time holding trunk in horizontal position prone over table edge. It will be recorded in seconds.

    Measured: up to 6 months

  10. Trunk Stabilization-Trunk flexor test

    Trunk stabilization will be evaluated using the Trunk flexor test test.The test measures core endurance. Time maintaining 60° trunk flexion with knees/hips at 90°. It will be recorded in seconds.

    Measured: up to 6 months

  11. Trunk Stabilization-Sit up test

    The 30-second Sit-up Test measures core strength. The person lies on their back with knees bent and feet on the floor. They do as many sit-ups as possible in 30 seconds, keeping proper form. The score is the number of correct sit-ups completed.

    Measured: up to 6 months

  12. Trunk Stabilization-Modifiye push up test

    The 30-second Modified Push-up Test measures core strength. The person starts in a push-up position but with knees on the floor. They perform as many push-ups as possible in 30 seconds, keeping the body straight and lowering the chest close to the ground. The score is the number of correct push-ups completed.

    Measured: up to 6 months

Timeline

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

  1. First posted3 Sep 2025
  2. Study start6 Aug 2025
  3. Primary completion31 Dec 2026 (estimated)
  4. Study completion1 Jan 2027 (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
Case only
Time perspective
Cross-sectional
Enrolment
50 participants (estimated)
Target duration
1 Day
IDs, dates and publications
ClinicalTrials.gov ID
NCT07151534
Sponsor's protocol ID
Body Awareness
Status last verified
Sep 2026
First submitted
6 Aug 2025
Last updated
17 Sep 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Multiple Sclerosis, run by Hacettepe 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 5 inclusion and 6 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: looking for participants now, as of the sponsor's last update on 17 Sep 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?

Contact Güngör Beyza Özvar Şenöz (5053888617 ext. +90, beyzaozvar@gmail.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Body Awareness Questionnaire (time frame: up to 6 months). The study lists 12 primary outcomes in all. 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 17 Sep 2026.

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