Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

Clinical Evaluation of Acupuncture on the Complications of Cerebral Vascular Accident

20. oktober 2015 opdateret af: China Medical University Hospital

The lifestyle of Taiwanese people has been changed over the past decade with the improvement of economic growth, environmental sanitation and the quality of medical care. Now the investigators pay more attention to the increasing risk of people's diseases of civilization than people's malnutrition and poor quality of environmental sanitation. The cerebrovascular accident (CVA) leads to death and bio-psycho-social dysfunction. The medical care of the patient of cerebrovascular accident cause a lot of money and is a burden of our country.

Our study emphasizes that acupuncture change bio-psycho-social aspects of the patient with cerebrovascular accident. The investigators use some scales to assess efficacy of acupuncture, such as Barthel index, National Institute of Health Stroke Scale, Visual Analogue Scale, Instrumental Activities of Daily Living and Hamilton Depression Rating Scale.

Besides, the investigators notice that there are few journals about acupuncture effect of treating depression following cerebral vascular accident. The investigators may underestimate the amount of people having post-stroke depression. So the investigators use Hamilton Depression Rating Scale to Assess the post-stroke depression of cerebral vascular accident patient.

By assessing bio-psycho-social level of CVA patient, the investigators hope this study will offer them more "Holistic Health Care".

Studieoversigt

Status

Afsluttet

Betingelser

Detaljeret beskrivelse

We want to assess the effect of acupuncture on stroke patients. The study is a double-blind randomized controlled trial. We need 80 patients altogether. The Inclusion Criteria:

(1)first time stroke(ischemic or hemorrhagic stroke) with paresis or plegia

Exclusion Criteria:

(1)transient ischemic attack (2)brain tumor, brain trauma (3)recurrent stroke (4)multiple organs failure, cancer The whole course of the acupuncture contains 24times(about 3 months). The acupoints are fixed and located over head and limbs.

The whole course of the sham acupuncture contains 24times(about 3 months). The acupoints are fixed and 1cm away from meridian and no acupoints over head were chosen.

The investigators use Barthel index, National Institute of Health Stroke Scale, Hamilton Depression Rating Scale, Instrumental activities of daily living scale and Visual Analogue Scale to assess the effect of acupuncture on stroke patients. Four times of assessment are as below: baseline, after 8th treatment, after 16th treatment, after 24th treatment (the last time of treatment). The course of treatment should be completed within 3 months.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

60

Fase

  • Fase 1

Kontakter og lokationer

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

Studiesteder

      • Taichung, Taiwan
        • Department of Acupuncture, China Medical University Hospital

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

40 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • first time stroke(ischemic or hemorrhagic stroke) with paresis or plegia

Exclusion Criteria:

  • transient ischemic attack
  • brain tumor, brain trauma
  • recurrent stroke
  • multiple organs failure, cancer

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: Dobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Acupuncture
The total course of the acupuncture contains 24times(about 3 months). The acupoints are fixed and located over head and limbs.

The whole course of the acupuncture contains 24times(about 3 months). The acupoints are fixed and located over head and limbs.

The whole course of the sham acupuncture contains 24times(about 3 months). The acupoints are fixed and 1cm away from meridian and no acupoints over head were chosen.

Andre navne:
  • acupuncture(4.4cm in length and 32-gauge)
  • shame acupuncture(1.27 cm in length and 40-gauge)
Sham-komparator: sham acupuncture
The total course of the acupuncture contains 24times(about 3 months). The acupoints are fixed and 1cm away from meridian and no acupoints over head were chosen.

The whole course of the acupuncture contains 24times(about 3 months). The acupoints are fixed and located over head and limbs.

The whole course of the sham acupuncture contains 24times(about 3 months). The acupoints are fixed and 1cm away from meridian and no acupoints over head were chosen.

Andre navne:
  • acupuncture(4.4cm in length and 32-gauge)
  • shame acupuncture(1.27 cm in length and 40-gauge)

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Change from baseline in Barthel index at 8 weeks
Tidsramme: Baseline and 8 weeks
Baseline and 8 weeks
Change from baseline in Barthel Index at 16 weeks
Tidsramme: Baseline, 16 weeks
Baseline, 16 weeks
Change from baseline in Barthel Index at 24 weeks
Tidsramme: Baseline, 24 weeks
Baseline, 24 weeks
Change from baseline in National Institute of Health Stroke Scale at 8 weeks
Tidsramme: Baseline, 8 weeks
Baseline, 8 weeks
Change from baseline in National Institute of Health Stroke Scale at 16 weeks
Tidsramme: Baseline, 16 weeks
Baseline, 16 weeks
Change from baseline in National Institute of Health Stroke Scale at 24 weeks
Tidsramme: Baseline, 24 weeks
Baseline, 24 weeks
Change from baseline in Instrumental Activities of Daily Living Scale at 8 weeks
Tidsramme: Baseline, 8 weeks
Baseline, 8 weeks
Change from baseline in Instrumental Activities of Daily Living Scale at 16 weeks
Tidsramme: Baseline, 16 weeks
Baseline, 16 weeks
Change from baseline in Instrumental Activities of Daily Living Scale at 24 weeks
Tidsramme: Baseline, 24 weeks
Baseline, 24 weeks
Change from baseline in Hamilton Depression Rating Scale at 8 weeks
Tidsramme: Baseline, 8 weeks
Baseline, 8 weeks
Change from baseline in Hamilton Depression Rating Scale at 16 weeks
Tidsramme: Baseline,16 weeks
Baseline,16 weeks
Change from baseline in Hamilton Depression Rating Scale at 24 weeks
Tidsramme: Baseline, 24 weeks
Baseline, 24 weeks

Sekundære resultatmål

Resultatmål
Tidsramme
Change from baseline in Visual Analogue Scale at 8 weeks
Tidsramme: Baseline, 8 weeks
Baseline, 8 weeks
Change from baseline in Visual Analogue Scale at 16 weeks
Tidsramme: Baseline,16 weeks
Baseline,16 weeks
Change from baseline in Visual Analogue Scale at 24 weeks
Tidsramme: Baseline, 24 weeks
Baseline, 24 weeks

Samarbejdspartnere og efterforskere

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

Efterforskere

  • Studieleder: Yu-Chen Lee, PHD, Department of Acupuncture, China Medical University 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

1. april 2013

Primær færdiggørelse (Faktiske)

1. juli 2015

Studieafslutning (Faktiske)

1. juli 2015

Datoer for studieregistrering

Først indsendt

8. juni 2014

Først indsendt, der opfyldte QC-kriterier

22. juli 2014

Først opslået (Skøn)

23. juli 2014

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

22. oktober 2015

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

20. oktober 2015

Sidst verificeret

1. oktober 2015

Mere information

Begreber relateret til denne undersøgelse

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 .

Abonner