- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01771887
Effects of Education Program for Lebanese Diabetic T2 in Their Behavior of Auto Managing, of Self-efficacy and Adhesion
3. december 2014 opdateret af: Randa Atallah, Université de Montréal
Assessing the Effects of Education Program for Lebanese Diabetic Type 2 in Their Behavior of Auto Managing Their Sense of Self-efficacy and on Their Adhesion Therapy
Diabetes mellitus is a disease of great frequency and is a major public health problem.
In Lebanon, the incidence of diabetes is estimated at 12%, it is expected to double by the year 2025.
Given the increasing prevalence of diabetes in Lebanon, the evolution of complications of this disease and the lack of studies at this level, it is appropriate to conduct a study that aims to evaluate the effects an education program for people with type 2 diabetes on their sense of self-efficacy and their ability to self-manage their disease to make them the most optimal therapeutic adherence possible.
The design of this study is experimental type before / after randomization by diabetic patients.
Education program delivered to the experimental group is the "Accu-Chek Education Program" of Roche.
Membership will be assessed using a biomarker HbA1c should be <7%, and a questionnaire (Summary of Diabetes Self-Care Activities Measure), which measures self-care behaviors.
Self-efficacy is measured using the Diabetes Management Self-Efficacy Scale.
And this before the intervention and 3 months later.
The sample will be 240 diabetic patients T2.
Recruitment will be in outpatient diabetology a Hospital located in Beirut.
Statistical analyzes used for descriptive variables are measures of central tendency, dispersion and frequency distribution.
T-test and chi-square will be used to compare the socio-demographic characteristics of the 2 groups, experimental and control.
To test hypotheses and determine the difference in the results of the dependent variables of the 2 groups, analysis of variance and covariance are used.
The data will be processed using SPSS version 14.0.
Studieoversigt
Status
Afsluttet
Betingelser
Intervention / Behandling
Detaljeret beskrivelse
- Following the implementation of a program of education, feeling of self-efficacy participants will be higher in the experimental group than in the control group.
- Following the implementation of a program of education, self-management behaviors: monitoring the diet, the practice of physical exercise, self-monitoring blood sugar, taking medications and care feet, participants will be higher in the experimental group than in the control group.
- Following the implementation of a program of education, the percentage of participants who have an HbA1c less than 7 will be higher in the experimental group than in the control group.
Undersøgelsestype
Interventionel
Tilmelding (Faktiske)
108
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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Beirut, Libanon, 16-6830
- Outpatient of hospital of Hotel Dieu de France
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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 80 år (Voksen, Ældre voksen)
Tager imod sunde frivillige
Ja
Køn, der er berettiget til at studere
Alle
Beskrivelse
Inclusion Criteria:
- 18 years and over,
- Suffering from type 2 diabetes for at least one year,
- Lebanese speak, read and write Arabic,
- Have an HbA1c ≥ 7%
Exclusion Criteria:
- mental impairment
- a psychological problem uncontrolled and medicated
Studieplan
Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Forebyggelse
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: education program
education program in 6 hours for groups of 10 people.
The content will be divided into 2 sessions with an interval of 2 weeks, the duration of each session is 3 hours.
Means active learning, teaching materials in Arabic accompany the content masterful discussions on flipcharts, situation analysis, computer-assisted presentation, demonstration, 150 photos of Lebanese dishes.
After, patients receive a 10-page illustrated book, a logbook of diabetes control. 2 weeks after the second education session, each participant will receive 5 calls every 15 days in 2 months.
During each call, the research assistant will ask the patient about diet, exercise and self-monitoring, medication and foot care and this according to a checklist.
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education program in 6 hours and monitoring phone every 15 days
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Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
adhesion
Tidsramme: HbA1c less than 7 % 3 months after the intervention
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HbA1c less than 7 % 3 months after the intervention
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Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Self-management behaviors
Tidsramme: improvement of self-management behaviors 3 months after the intervention
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self-management behaviors will be measured using a questionnaire of 25 questions, Summary of Diabetes Self-Care Activities Measure SDSCA, which measures five behaviors: diet, exercise, self monitoring blood glucose, medication and foot care (Toobert et al., 2000).
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improvement of self-management behaviors 3 months after the intervention
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Andre resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
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self-efficacy
Tidsramme: enhancement of the sense of self-efficacy 3 months after the intervention
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Self-efficacy is measured using the Diabetes Management Self-Efficacy Scale (DMSES).
This instrument was developed in 1999 by van der Bijl, van Poelgeest-Shortridge-Bagget & Eeltink.
This instrument consists of 20 items.
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enhancement of the sense of self-efficacy 3 months after the intervention
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Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Efterforskere
- Studieleder: José Côté, nur. Ph. D., Université de Montréal
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. februar 2013
Primær færdiggørelse (Faktiske)
1. september 2013
Studieafslutning (Faktiske)
1. december 2014
Datoer for studieregistrering
Først indsendt
8. januar 2013
Først indsendt, der opfyldte QC-kriterier
16. januar 2013
Først opslået (Skøn)
18. januar 2013
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
4. december 2014
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
3. december 2014
Sidst verificeret
1. december 2014
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- ATALLAH-FSI-6
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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