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Sensorimotor Training With a Mobilized Balance Platform in Patients With Chronic Low Back Pain

16. maj 2026 opdateret af: Sefa Gümrük Aslan, Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Effects of a Sensorimotor Training Protocol Using a Mobilized Balance Platform on Proprioceptive System, Movement Control, and Quality of Life in Patients With Chronic Low Back Pain

This randomized controlled study aims to investigate the effects of a sensorimotor training protocol using a mobilized balance platform device on proprioceptive system function, movement control, balance, physical performance, pain severity, and quality of life in patients with chronic low back pain. A total of 44 patients with chronic low back pain will be recruited from the outpatient clinic of Gaziler Physical Medicine and Rehabilitation Training and Research Hospital.

Participants will be randomly assigned to either a sensorimotor training group or a control group. The intervention group will receive sensorimotor training using the Huber 360 balance system, while the control group will perform a home exercise program including stretching, spinal mobility, lumbopelvic control, and balance exercises.

Pain severity, proprioception, functional status, balance, physical performance, and quality of life will be assessed before and after treatment by an assessor blinded to group allocation.

Studieoversigt

Status

Rekruttering

Betingelser

Intervention / Behandling

Undersøgelsestype

Interventionel

Tilmelding (Anslået)

44

Fase

  • Ikke anvendelig

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiekontakt

Studiesteder

  • Tyrkiet (Türkiye)
      • Ankara, Tyrkiet (Türkiye)
        • Rekruttering
        • Ankara Gaziler physical therapy and rehabilitation hospital
        • Kontakt:

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

  • Voksen

Tager imod sunde frivillige

Ingen

Beskrivelse

Inclusion Criteria:

  • Individuals aged between 18 and 55 years
  • Presence of chronic low back pain lasting at least 3 months
  • Pain intensity score of 3 or higher on the Visual Analog Scale (VAS)
  • Individuals with sufficient cognitive ability to understand and follow study procedures
  • Willingness to participate voluntarily in the study

Exclusion Criteria:

  • Participation in a similar training program within the last 12 months
  • History of lower extremity or spinal surgery
  • Presence of non-mechanical low back pain, inflammatory disease, or tumor
  • Uncontrolled hypertension or cardiac disease
  • History of malignancy
  • Presence of radicular symptoms associated with low back pain
  • Progressive neurological deficits
  • Neurogenic claudication

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Enkelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Aktiv komparator: Home Exercise Program
Participants in this group will perform a home exercise program including warm-up and stretching exercises, spinal mobility exercises, lumbopelvic control exercises, and balance exercises. The program will be performed for 30 minutes per session, twice weekly for 5 weeks.
Adfærdsmæssigt: Home Exercise Program
Participants will perform a home exercise program including warm-up and stretching exercises, spinal mobility exercises, lumbopelvic control exercises, and balance exercises. The program will be performed for 30 minutes per session, twice weekly for 5 weeks.
Eksperimentel: Huber 360 Sensorimotor Training
Participants in this group will receive a sensorimotor training protocol using the Huber 360 balance system. The intervention will include progressive rotational and oscillatory exercises aimed at improving proprioception, balance, neuromuscular control, and movement control. Sessions will be performed for 30 minutes, twice weekly for 5 weeks.
Adfærdsmæssigt: Home Exercise Program
Participants will perform a home exercise program including warm-up and stretching exercises, spinal mobility exercises, lumbopelvic control exercises, and balance exercises. The program will be performed for 30 minutes per session, twice weekly for 5 weeks.
Enhed: Huber 360 Sensorimotor Training
Participants will receive sensorimotor training using the Huber 360 balance system. The protocol will include progressive rotational and oscillatory exercises designed to improve proprioception, balance, neuromuscular control, and movement control in patients with chronic low back pain. Sessions will be performed for 30 minutes, twice weekly for 5 weeks.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Lumbar Proprioception Assessment
Tidsramme: Before treatment and immediately after completion of the 5-week intervention program
Lumbar proprioception will be assessed using lumbar repositioning tests at 60 degrees flexion and 15 degrees extension. Participants will be asked to reproduce target lumbar positions, and the angular repositioning error will be recorded. Lower repositioning error values indicate better lumbar proprioceptive accuracy.
Before treatment and immediately after completion of the 5-week intervention program

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Pain Severity Assessed by Visual Analog Scale
Tidsramme: Before treatment and immediately after completion of the 5-week intervention program
Pain intensity will be assessed using a 10-cm Visual Analog Scale (VAS). Scores range from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain severity.
Before treatment and immediately after completion of the 5-week intervention program
Functional Status Assessed by Oswestry Disability Index
Tidsramme: Before treatment and immediately after completion of the 5-week intervention program
Functional disability related to low back pain will be assessed using the Oswestry Disability Index (ODI). Higher scores indicate greater disability.
Before treatment and immediately after completion of the 5-week intervention program
Balance and Limits of Stability Assessed by Huber 360
Tidsramme: Before treatment and immediately after completion of the 5-week intervention program
Static balance, dynamic balance, and limits of stability will be assessed using the Huber 360 balance system. Better balance performance and improved stability limits indicate better postural control.
Before treatment and immediately after completion of the 5-week intervention program
Lumbar Flexion Range of Motion
Tidsramme: Before treatment and immediately after completion of the 5-week intervention program
Physical performance will be assessed using a Physical Performance Test Battery including lumbar flexion range of motion, 50-step walking test, 5-minute walking test, five-repetition sit-to-stand test, ten-repetition trunk flexion test, and forward reaching with weight.
Before treatment and immediately after completion of the 5-week intervention program
Quality of Life Assessed by Short Form-36
Tidsramme: Before treatment and immediately after completion of the 5-week intervention program
Quality of life will be assessed using the Short Form-36 (SF-36). Higher scores indicate better health-related quality of life.
Before treatment and immediately after completion of the 5-week intervention program
50-Step Walking Test
Tidsramme: Before treatment and immediately after completion of the 5-week intervention program
he time required to complete the 50-step walking test will be recorded in seconds
Before treatment and immediately after completion of the 5-week intervention program
Five-Minute Walking Test
Tidsramme: Before treatment and immediately after completion of the 5-week intervention program
The time required to complete five sit-to-stand repetitions will be recorded in seconds.
Before treatment and immediately after completion of the 5-week intervention program
Ten-Repetition Trunk Flexion Test
Tidsramme: Before treatment and immediately after completion of the 5-week intervention program
The time required to complete ten trunk flexion repetitions will be recorded in seconds.
Before treatment and immediately after completion of the 5-week intervention program
Forward Reaching with Weight Test
Tidsramme: Before treatment and immediately after completion of the 5-week intervention program
Forward reaching distance while holding weight will be measured in centimeters.
Before treatment and immediately after completion of the 5-week intervention program

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

4. maj 2026

Primær færdiggørelse (Anslået)

30. oktober 2026

Studieafslutning (Anslået)

30. november 2026

Datoer for studieregistrering

Først indsendt

3. maj 2026

Først indsendt, der opfyldte QC-kriterier

16. maj 2026

Først opslået (Faktiske)

22. maj 2026

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

22. maj 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

16. maj 2026

Sidst verificeret

1. maj 2026

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • CLBP-MBP-2026

Plan for individuelle deltagerdata (IPD)

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