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Effect of Anterioposterior Weight Shifting Training With Visual Biofeedback in Subacute Stroke

16. november 2020 opdateret af: Yonsei University

Asymmetric gait patterns of stroke is one of the most important functional activities to enable community participation, it is major goal for stroke patients. Reported that the stroke patients had asymmetry at stance time, single stance, double support time, and swing time compared to normal people, and claimed that the most important factor was step length. According to Albert et al., patients with an asymmetric gait pattern have a long double support phase and a healthy side single support phase, and less weight shift to the affected side. Recent studies have shown that visual feedback for weight shift may be helpful to obtain a symmetrical posture after stroke. However, no study has been conducted on the therapeutic effect on gait asymmetry and patterns. We aimed to investigate the effect of Anterioposterior Weight Shifting Training with Visual Biofeedback in subacute post-stroke patients on gait asymmetry and pattern.

40 subacute post-stroke patients with Step Length Asymmetry were enrolled in this study. The subjects were randomly assigned into two groups. The training group received an additional anterioposterior weight shifting training with visual Biofeedback 5 times per week for 4weeks. The control group received the usual gait training. The spatiotemporal and kinematic data were obtained during walking through 3D motion analysis. Functional Ambulation Category, Self-selected walking speed, Maximum safe walking speed, Berg balance Test (BBT), Fugl-Meyer Assessment (FMA), Medical Research Council Score (MRC), Functional Independent Measure-mobility, Timed Up and Go test (TUG) were assessed at pre, during, post- training, and 4week follow-up. Those were compared between two groups by repeated measures ANOVA.

Studieoversigt

Undersøgelsestype

Interventionel

Tilmelding (Forventet)

50

Fase

  • Ikke anvendelig

Kontakter og lokationer

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

Studiesteder

      • Seoul, Korea, Republikken
        • Rekruttering
        • Department and Research Institute of Rehabilitation Medicine, Yonsei University College of Medicine
        • Kontakt:
          • Deog Young Kim
          • Telefonnummer: +82-2-2228-3714
          • E-mail: KIMDY@yuhs.ac

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

19 år til 90 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  1. less than 6 months after onset of the stroke
  2. can stand and walk independently 10m
  3. K-MMSE score of at least 15
  4. have asymmetrical gait pattern with Step length asymmetric ratio greater than 1.1
  5. over 20 years of age.

Exclusion Criteria:

  1. quadriplegia
  2. past history of stroke
  3. past history of Musculoskeletal disease or history of Neurological diseases

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: Ingen (Åben etiket)

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Andet: Kontrolgruppe
The control group received the usual gait training.
Eksperimentel: Træningsgruppe

The training group received an additional anterioposterior weight shifting training with visual Biofeedback 5 times per week for 4weeks. AP training is made to instantly know your training status during training by measuring and processing the foot pressure in real time using the F-Scan (Tekscan) hardware system and Software Development Kit (SDK).

Before training, all patients are instructed to place both feet at shoulder width, place the inverted foot approximately 30 cm in front of the unaffected side foot, move the body forward with the chest straight in an upright position, and be instructed to put the weight on the affected side.

On the screen shown, measure the maximum weight distribution during the first 10 times and set the value added by 5% as the target value.

It is designed to induce the maximum weight shift through the archery game.

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Step Length Asymmetric Ratio
Tidsramme: before training(0week)
Step Length Asymmetric Ratio = paretic step length/non paretic step length
before training(0week)
Step Length Asymmetric Ratio
Tidsramme: during training(2week)
Step Length Asymmetric Ratio = paretic step length/non paretic step length
during training(2week)
Step Length Asymmetric Ratio
Tidsramme: after training(4week)
Step Length Asymmetric Ratio = paretic step length/non paretic step length
after training(4week)
Step Length Asymmetric Ratio
Tidsramme: Follow up(8week)
Step Length Asymmetric Ratio = paretic step length/non paretic step length
Follow up(8week)
Step Length Asymmetric Index
Tidsramme: before training(0week)
Step Length Asymmetric Index = paretic step length-non paretic step length/0.5[paretic step length +non paretic step length]
before training(0week)
Step Length Asymmetric Index
Tidsramme: during training(2week)
Step Length Asymmetric Index = paretic step length-non paretic step length/0.5[paretic step length +non paretic step length]
during training(2week)
Step Length Asymmetric Index
Tidsramme: after training(4week)
Step Length Asymmetric Index = paretic step length-non paretic step length/0.5[paretic step length +non paretic step length]
after training(4week)
Step Length Asymmetric Index
Tidsramme: Follow up(8week)
Step Length Asymmetric Index = paretic step length-non paretic step length/0.5[paretic step length +non paretic step length]
Follow up(8week)

Samarbejdspartnere og efterforskere

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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

1. oktober 2014

Primær færdiggørelse (Forventet)

1. juni 2021

Studieafslutning (Forventet)

1. juni 2021

Datoer for studieregistrering

Først indsendt

16. november 2020

Først indsendt, der opfyldte QC-kriterier

16. november 2020

Først opslået (Faktiske)

20. november 2020

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

20. november 2020

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

16. november 2020

Sidst verificeret

1. november 2020

Mere information

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