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Temporal and Kinematic Analysis of Timed Up and Go Test in Chronic Low Back Pain Patients

8. oktober 2020 opdateret af: Riccardo Buraschi, Fondazione Don Carlo Gnocchi Onlus

Temporal and Kinematic Analysis of Timed Up and Go Test in Chronic Low Back Pain

Kinematic and temporal analysis of the movement helps researchers and clinicians to better understand the way humans move and interact within the environment in which they live, better describe the alterations coming from impairments, and finally allow to better tailor interventions for patients. In this perspective, motion analysis has become, in the last 30 years, a remarkable and important field of research. Even if movement assessment should be a cornerstone for definition and modulation of rehabilitation interventions, there are still few motion analysis devices that are able to influence the clinical decision process; motion analysis labs are among those, but their use is unfortunately limited due to the costs of instruments and analysis. Other small unobtrusive wearable devices, easier to use and cost-effective, have been developed, like Inertial measurement units (IMU), composed by accelerometers and gyroscopes. They could therefore represent an incentive for a more widespread use of motion analysis within daily clinical activity in Rehabilitaion.

Timed Up and Go Test (TUG) is a simple, widely used, functional test which involves standing up from a chair, walking three meters, turning, and going back to sit. It is used to evaluate movement, mobility, dynamic and static balance in people with musculoskeletal impairment, neurological diseases, aging related conditions, and the quality of life in people with low back pain. The only and easy outcome considered is the time to completion. Nevertheless, the application of an IMU to a subject performing TUG can provide other objective, quantitative data, like temporal and kinematic parameters of the whole test and its sub-phases. The instrumented TUG (iTUG) has already been applied, mainly in the neurorehabilitation field, in particular for Parkinson's disease and for post-stroke impairments.

cLBP is one of the most burdensome health problem worldwide. cLBP has been considered a bio-psycho-social disease, characterized by pain in the lumbar region, functional impairments, and condition-related disability. Despite the obvious motor problems affecting people with cLBP, to the best of our knowledge, chronic low back pain (cLBP) has not yet been explored using iTUG.

The aim of study is to analyse temporal and kinematic parameters of cLBP subjects compared to BMI and age-matched healthy subjects, through iTUG and to explore the correlations of those parameters with pain and disability.

Studieoversigt

Status

Afsluttet

Undersøgelsestype

Observationel

Tilmelding (Faktiske)

44

Kontakter og lokationer

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Studiesteder

    • Brescia
      • Rovato, Brescia, Italien, 25038
        • Fondazione Don Carlo Gnocchi Onlus - Centro Ettore Spalenza

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

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ja

Køn, der er berettiget til at studere

Alle

Prøveudtagningsmetode

Ikke-sandsynlighedsprøve

Studiebefolkning

Population of Chronic Low Back Pain subjects participating to an outpatient rehabilitation program; Population of healthy subjects, age and BMI-matched with the Low Back Pian sample.

Beskrivelse

Inclusion Criteria (for Chronic Low Back Pain population):

  • Pain from at least 3 months
  • Numerical Pain Rating Scale (NPRS) ≥ 4

Exclusion Criteria (for Chronic Low Back Pain population):

  • History of neurological impairment or disease,
  • Other orthopaedic impairment within the past 6 months or surgery in the previous 6 months.

Studieplan

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

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

Kohorter og interventioner

Gruppe / kohorte
Intervention / Behandling
Chronic Low-Back Pain
Subjects diagnosed with Chronic Low-Back Pain in rehabilitation program: functional assessment (with temporal and kinematic analysis) and clinical assessment.
Timed Up and Go Test administration with application of Inertial Measurement Unit for a temporal and kinematic assessment of movement performed during test esecution

Roland Morris Disability Questionnaire (RMDQ) to assess the level of functional impairment and disability in the activity of daily living

Numerical Pain Rating System (NPRS) administration to quantify level of pain experienced just before the TUG test execution

Healthy
Healthy subjects: functional assessment (with temporal and kinematic analysis)
Timed Up and Go Test administration with application of Inertial Measurement Unit for a temporal and kinematic assessment of movement performed during test esecution

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Temporal parameters of movement
Tidsramme: through study completion, an average of 2 month
Temporal analysis of TUG performance
through study completion, an average of 2 month
Kinematic parameters of movement
Tidsramme: through study completion, an average of 2 month
Kinematic analysis of TUG performance
through study completion, an average of 2 month

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Roland Morris Disability Questionnaire
Tidsramme: through study completion, an average of 2 month
Questionnaire that assess levels of impairment and disability coming from low back pain The score can range from 0 (no disability) to 24 (severe disability).
through study completion, an average of 2 month
Numerical Pain Rating Scale
Tidsramme: through study completion, an average of 2 month
Scale for pain assessment: the minimum value "0" and maximum values "10", where higher scores mean a worse outcome.
through study completion, an average of 2 month

Samarbejdspartnere og efterforskere

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Datoer for undersøgelser

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Studer store datoer

Studiestart (Faktiske)

9. december 2019

Primær færdiggørelse (Faktiske)

30. januar 2020

Studieafslutning (Faktiske)

30. januar 2020

Datoer for studieregistrering

Først indsendt

17. september 2020

Først indsendt, der opfyldte QC-kriterier

8. oktober 2020

Først opslået (Faktiske)

19. oktober 2020

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

19. oktober 2020

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

8. oktober 2020

Sidst verificeret

1. oktober 2020

Mere information

Begreber relateret til denne undersøgelse

Yderligere relevante MeSH-vilkår

Andre undersøgelses-id-numre

  • TUGLBP_FDG

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