- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT02460809
Home-based Non-invasive Brain Stimulation and Hand Tracking Rehabilitation for People With Chronic Stroke
9. maj 2019 opdateret af: University of Minnesota
Home-based tDCS and Hand Tracking Rehabilitation for Chronic Stroke
This is a device feasibility study, which will assess telerehabilitation in people with chronic stroke using a combination of noninvasive brain stimulation and finger tracking training.
Telerehabilitation allows patients to train in their own home which also allows for longer training periods than what is currently allowed clinically.
Noninvasive transcranial direct current stimulation (tDCS) uses two surface electrodes connected to a small battery that will be attached to the head.
This will be used to modulate neuronal excitability.
With sensors attached to fingers and the wrist, the patient will move the joints to track a target displayed on a screen.
The combined treatment will be applied in two experiments.
The first will be on 3 patients coming to our lab and the second on 3 patients in their home, both under supervision.
We will integrate the two components and test the resulting and novel treatment system for technical feasibility, which will set the stage for future efficacy studies under federal grant support.
We hypothesize that the developed system will be safe and feasible.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This study will assess the feasibility of a telerehabilitation protocol involving non-invasive brain stimulation.
Therefore, the two arms of the study are 1) implementation of this protocol in a controlled laboratory setting and 2) implementation of this protocol in a patient's home, being set up by the patient but controlled remotely using a blue-tooth system by an investigator in a different location.
The two arms of this study will occur successively with the first arm being completed with three patients followed by the second arm being completed with a second group of three patients.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
6
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
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Minnesota
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Minneapolis, Minnesota, Forenede Stater, 55455
- University of Minnesota
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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
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- adult at least 18 years old
- stroke duration >6 months,
- Mini-Mental State Examination score 24 or higher
- presence of tactile sensation on the scalp
- at least 10 degrees of active finger or wrist motion in the stroke hand
- ability to walk 100 feet and transfer independently
Exclusion Criteria:
- seizure within past two years
- pregnancy
- metal inside the had (dental metal is permitted)
- implanted medical devices incompatible with tDCS
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Enhedens gennemførlighed
- Tildeling: Ikke-randomiseret
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
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Aktiv komparator: In-lab tDCS
Three people with chronic stroke will participate in finger tracking training while receiving transcranial direct current stimulation (tDCS) in a controlled laboratory environment with an investigator.
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Transcranial direct current stimulation (tDCS) uses two surface electrodes placed on the scalp.
These electrodes pass a low voltage current and modulate membrane potentials of underlying neurons.
|
Eksperimentel: In-home tDCS
Three people with chronic stroke will participate in finger tracking training while receiving transcranial direct current stimulation (tDCS) in their own home.
Patients will be taught how to use a blue-tooth enabled telerehabilitation module that is being controlled by an investigator in the lab on the University campus.
For safety, an investigator will be in the home with each patient during tDCS use and finger tracking training but will only be supervising procedures.
|
Transcranial direct current stimulation (tDCS) uses two surface electrodes placed on the scalp.
These electrodes pass a low voltage current and modulate membrane potentials of underlying neurons.
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
---|---|---|
Digit Span
Tidsramme: First day of study and one day following the final treatment
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Short-term memory test using single numerical digits
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First day of study and one day following the final treatment
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Box and block
Tidsramme: First day of study and one day following the final treatment
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Finger dexterity test using both paretic and nonparetic hands
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First day of study and one day following the final treatment
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Quantification of Compliance Questionnaire
Tidsramme: First day of study and one day following the final treatment
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First day of study and one day following the final treatment
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User perception survey
Tidsramme: First day of study and one day following the final treatment
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Survey
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First day of study and one day following the final treatment
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Sekundære resultatmål
Resultatmål |
Tidsramme |
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Survey of symptoms questionnaire
Tidsramme: Each day of study as well as one day following the final treatment
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Each day of study as well as one day following the final treatment
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Ledende efterforsker: James Carey, PhD, PT, University of Minnesota
Publikationer og nyttige links
Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.
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)
1. januar 2017
Primær færdiggørelse (Faktiske)
1. maj 2017
Studieafslutning (Faktiske)
1. maj 2017
Datoer for studieregistrering
Først indsendt
29. maj 2015
Først indsendt, der opfyldte QC-kriterier
29. maj 2015
Først opslået (Skøn)
2. juni 2015
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
13. maj 2019
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
9. maj 2019
Sidst verificeret
1. maj 2019
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- Home tDCS
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Ingen
Studerer et amerikansk FDA-reguleret enhedsprodukt
Ja
produkt fremstillet i og eksporteret fra U.S.A.
Ingen
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
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