- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01771887
Effects of Education Program for Lebanese Diabetic T2 in Their Behavior of Auto Managing, of Self-efficacy and Adhesion
3 december 2014 uppdaterad av: 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.
Studieöversikt
Detaljerad beskrivning
- 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.
Studietyp
Interventionell
Inskrivning (Faktisk)
108
Fas
- Inte tillämpbar
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studieorter
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Beirut, Libanon, 16-6830
- Outpatient of hospital of Hotel Dieu de France
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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
18 år till 80 år (Vuxen, Äldre vuxen)
Tar emot friska volontärer
Ja
Kön som är behöriga för studier
Allt
Beskrivning
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
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Förebyggande
- Tilldelning: N/A
- Interventionsmodell: Enskild gruppuppgift
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Experimentell: 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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Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
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adhesion
Tidsram: 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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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Self-management behaviors
Tidsram: 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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Andra resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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self-efficacy
Tidsram: 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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Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Sponsor
Utredare
- Studierektor: José Côté, nur. Ph. D., Université de Montréal
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 februari 2013
Primärt slutförande (Faktisk)
1 september 2013
Avslutad studie (Faktisk)
1 december 2014
Studieregistreringsdatum
Först inskickad
8 januari 2013
Först inskickad som uppfyllde QC-kriterierna
16 januari 2013
Första postat (Uppskatta)
18 januari 2013
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
4 december 2014
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
3 december 2014
Senast verifierad
1 december 2014
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- ATALLAH-FSI-6
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