- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01475422
Effectiveness of the Self Monitoring of Capillary Blood Glucose at Home
16. november 2011 opdateret af: Vívian Saraiva Veras, University of Sao Paulo
Effectiveness of the Self Monitoring of Capillary Blood Glucose at Home in Metabolic Control of People With Diabetes Mellitus
The self-monitoring of capillary blood glucose is part of the package of interventions in diabetes mellitus and an effective therapeutic strategy for the adequate control of the disease; and the continuing education of people with DM is recognized as one of the goals to delay the complications arising from chronic disease and alleviate the symptoms of hypoglycemia and hyperglycemia.
Studieoversigt
Status
Ukendt
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
This study aims to evaluate the effects of educational intervention on self-monitoring of capillary blood glucose in metabolic control, knowledge and attitude in two groups of patients with diabetes mellitus: a group of diabetic patients who participate in the Self-Monitoring of Capillary Blood Glucose at Home Program and receive educational interventions (Intervention Group - G1) and a group of diabetic patients who participle in the Self-Monitoring of Capillary Blood Glucose at Home Program and receive conventional treatment (Control Group - G2).
As an educational tool in diabetes will be used Conversation Maps which is considered an interactive program of diabetes education.
Undersøgelsestype
Interventionel
Tilmelding (Forventet)
91
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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São Paulo
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Ribeirão Preto, São Paulo, Brasilien
- Rekruttering
- University of Sao Paulo
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Kontakt:
- Vívian Saraiva Veras, Principal Investigator
- Telefonnummer: 55 16 88074113
- E-mail: vivianveras@hotmail.com
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Ledende efterforsker:
- Vívian Saraiva Veras
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Underforsker:
- Maria Lúcia Zanetti, Study Chair
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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 til 90 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ingen
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- Ages 18 Years and older;
- Diagnosis of type 1 and 2 diabetes mellitus;
- In follow-up in the Self-Monitoring of Capillary Blood Glucose at Home Program;
- Have cognitive conditions that enable participation (minimum ability of users to understand issues of data collection instruments, observation of the researcher and/or of the caregivers).
Exclusion Criteria:
- Patients with gestational DM;
- Patients with DM who are not located;
- Those who die in the proposed period for the research;
- Those who dropout the Self-Monitoring of Capillary Blood Glucose at Home Program;
- Those who report difficulties to participate of the study due to work and those with amaurosis;
- Used Conversation Maps as an educational tool.
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Støttende pleje
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
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Aktiv komparator: Sædvanlig pleje
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Patients are followed in the medical appointments for evaluation and treatment of diabetes mellitus, according to service routine.
Participants will be followed for an expected average of 12 weeks.
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Eksperimentel: Conversation Maps Diabetes Education
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The Conversation Maps program is a set of innovative, interactive diabetes education tools developed by the Healthy Interactions, and endorsed by the American Diabetes Association.
It consists of four conversation maps covering: 1) how the body and diabetes works, 2) healthy eating and physical activity, 3) treatment with medication and monitoring blood glucose, and 4) reaching the targets with insulin (a fifth map covering gestational diabetes will not be used in this study), and a program manual to help educators successfully implement the program.
Participants will be followed for an expected average of 12 weeks.
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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HbA1c
Tidsramme: baseline, 3 and 6 months post intervention
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Change from baseline in HbA1c at 6 months to less than 7%
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baseline, 3 and 6 months post intervention
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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Diabetes Knowledge Questionnaire - DKN-A
Tidsramme: baseline, 3 and 6 months post intervention
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Change from baseline in DKN-A at six months
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baseline, 3 and 6 months post intervention
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Diabetes Attitude Questionnaire - ATT-19
Tidsramme: baseline, 3 and 6 months post intervention
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Change from baseline in ATT-19 at six months
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baseline, 3 and 6 months post intervention
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
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. september 2011
Primær færdiggørelse (Forventet)
1. december 2011
Studieafslutning (Forventet)
1. marts 2012
Datoer for studieregistrering
Først indsendt
10. november 2011
Først indsendt, der opfyldte QC-kriterier
16. november 2011
Først opslået (Skøn)
21. november 2011
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
21. november 2011
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
16. november 2011
Sidst verificeret
1. november 2011
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- 6266936
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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