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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02528162
Other study ID # the ELENA study
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2015
Est. completion date June 2019

Study information

Verified date November 2017
Source Universitaire Ziekenhuizen Leuven
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Prospective observational cohort study of women with gestational diabetes (GDM) based on the 'International Association of Pregnancy Study Groups' (IADPSG) criteria. The overall aim is to evaluate the knowledge regarding GDM of women with GDM and to evaluate the satisfaction of women with GDM about the education they receive (given in group or individually). Normal routine care is followed and evaluated.


Recruitment information / eligibility

Status Completed
Enrollment 200
Est. completion date June 2019
Est. primary completion date May 2019
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 45 Years
Eligibility Inclusion Criteria: - Women = 18 years diagnosed with GDM in the university hospital Leuven. Exclusion Criteria: - Women who received bariatric surgery. - Women with pregestational diabetes or diagnosed with diabetes during early pregnancy.

Study Design


Intervention

Behavioral:
education
Evaluation of education for GDM

Locations

Country Name City State
Belgium UZ Leuven Leuven

Sponsors (1)

Lead Sponsor Collaborator
Universitaire Ziekenhuizen Leuven

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of the knowledge regarding GDM with a self-designed questionnaire over a 2-4 week period
Primary Scale (0 to 3) with questionnaire on depression (CES-D ) over a 2-4 week period
Primary Evaluation of satisfaction with education and Diabetes Treatment Satisfaction Questionnaire over a 2-4 week period
Primary Scale (1-4) with questionnaire on anxiety (six-item short form STAI) over a 2-4 week period
Secondary The prevalence of GDM based on the IADPSG criteria at 24-28 weeks of pregnancy
Secondary Composite endpoint of glycaemic control, weight, gestational weight gain and pregnancy outcomes over a period of 16 weeks
Secondary The frequency of insulin therapy for GDM over a period of 16 weeks
Secondary The time between the glucose challenge test and oral glucose tolerance test at 24-28 weeks of pregnancy
Secondary The frequency of an HbA1c =6.5% at 24-28 weeks of pregnancy
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