- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT04637737
Effect of Anterioposterior Weight Shifting Training With Visual Biofeedback in Subacute Stroke
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
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Forventet)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
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Seoul, Korea, Republikken
- Rekruttering
- Department and Research Institute of Rehabilitation Medicine, Yonsei University College of Medicine
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Kontakt:
- Deog Young Kim
- Telefonnummer: +82-2-2228-3714
- E-mail: KIMDY@yuhs.ac
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Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- less than 6 months after onset of the stroke
- can stand and walk independently 10m
- K-MMSE score of at least 15
- have asymmetrical gait pattern with Step length asymmetric ratio greater than 1.1
- over 20 years of age.
Exclusion Criteria:
- quadriplegia
- past history of stroke
- past history of Musculoskeletal disease or history of Neurological diseases
Studieplan
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 |
|---|---|
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Andet: Kontrolgruppe
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The control group received the usual gait training.
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Eksperimentel: Træningsgruppe
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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)
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Step Length Asymmetric Ratio = paretic step length/non paretic step length
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before training(0week)
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Step Length Asymmetric Ratio
Tidsramme: during training(2week)
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Step Length Asymmetric Ratio = paretic step length/non paretic step length
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during training(2week)
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Step Length Asymmetric Ratio
Tidsramme: after training(4week)
|
Step Length Asymmetric Ratio = paretic step length/non paretic step length
|
after training(4week)
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Step Length Asymmetric Ratio
Tidsramme: Follow up(8week)
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Step Length Asymmetric Ratio = paretic step length/non paretic step length
|
Follow up(8week)
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Step Length Asymmetric Index
Tidsramme: before training(0week)
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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
Sponsor
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Forventet)
Studieafslutning (Forventet)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 4-2014-0383
Plan for individuelle deltagerdata (IPD)
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