Denna sida har översatts automatiskt och översättningens korrekthet kan inte garanteras. Vänligen se engelsk version för en källtext.

Clinical Evaluation of Acupuncture on the Complications of Cerebral Vascular Accident

20 oktober 2015 uppdaterad av: 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".

Studieöversikt

Status

Avslutad

Betingelser

Detaljerad beskrivning

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.

Studietyp

Interventionell

Inskrivning (Faktisk)

60

Fas

  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

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

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

40 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

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

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Dubbel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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.

Andra namn:
  • acupuncture(4.4cm in length and 32-gauge)
  • shame acupuncture(1.27 cm in length and 40-gauge)
Sham Comparator: 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.

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

Vad mäter studien?

Primära resultatmått

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

Sekundära resultatmått

Resultatmått
Tidsram
Change from baseline in Visual Analogue Scale at 8 weeks
Tidsram: Baseline, 8 weeks
Baseline, 8 weeks
Change from baseline in Visual Analogue Scale at 16 weeks
Tidsram: Baseline,16 weeks
Baseline,16 weeks
Change from baseline in Visual Analogue Scale at 24 weeks
Tidsram: Baseline, 24 weeks
Baseline, 24 weeks

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

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

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart

1 april 2013

Primärt slutförande (Faktisk)

1 juli 2015

Avslutad studie (Faktisk)

1 juli 2015

Studieregistreringsdatum

Först inskickad

8 juni 2014

Först inskickad som uppfyllde QC-kriterierna

22 juli 2014

Första postat (Uppskatta)

23 juli 2014

Uppdateringar av studier

Senaste uppdatering publicerad (Uppskatta)

22 oktober 2015

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

20 oktober 2015

Senast verifierad

1 oktober 2015

Mer information

Termer relaterade till denna studie

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

Prenumerera