CClinicalTrials.gg
Status unknownNCT02945540SATISFYDGUpdated Oct 26, 2016

Assessment of Patient Satisfaction Program "Gestational Diabetes"

An observational study in Gestational Diabetes, sponsored by University Hospital, Caen. Status unknown at 1 site in France. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2016-10-26.

Sponsored by University Hospital, Caen · Observational

The sponsor has not verified this record recently (last verified Sep 2016), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
350
Ages
18 Years and older
Sex
Female
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Study summary

This study seeks to evaluate patient satisfaction within the patient therapeutic education program "gestational diabetes" (multidisciplinary and multi-professional program) to see if they deem effective to limit the impact of gestational diabetes on pregnancy . Patients are questioned on the skills acquired in everyday life, the effective support in personal development, development of self-determination capabilities and communication with health professionals.

This study must include all patients participating in the therapeutic education program for a year and meeting the inclusion criteria.

02

Conditions studied

  • Gestational Diabetes

Keywords

  • Gestational diabetes
  • Patient education
  • Patient Satisfaction
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In context

Diabetes, Gestational

842 studies on the registry are indexed under Diabetes, Gestational; 198 are open to participants now.

This study's planned enrollment of 350 is above the median of 200 across 269 observational studies indexed under Diabetes, Gestational.

Browse Diabetes, Gestational studies →

Lead sponsor

University Hospital, Caen is the lead sponsor of 505 studies on the registry; 80 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Pregnant women with gestational diabetes and cared in therapeutic patient education

Inclusion criteria

  • pregnant women
  • Gestational diabetes diagnosis based on OGTT glucose 75g, performed after 24 weeks of gestation
  • Women aged 18 and over
  • After 24th week of gestation
  • Before 36th week of gestation
  • initial management in therapeutic education at the University Hospital of Caen

Exclusion criteria

Exclusion Criteria:

  • Another form of diabetes (existing before pregnancy or diagnosed before 24 weeks of gestation)
  • women under 18 years
  • Initial management of gestational diabetes by health professionals outside the University Hospital of Caen
  • Poor understanding of the French language
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
350 participants (estimated)
Patient registry
No
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What researchers measure

Primary outcomes

  1. Measuring patient satisfaction by a questionnaire on therapeutic education

    Evaluation of satisfaction the entry into the program, after the diagnosis, until the 36th week of gestation.

    Time frame: 36th week of gestation

  2. Measuring patient satisfaction at childbirth by a questionnaire on satisfaction of hospital care

    Assessment of satisfaction between the 36th week of gestation and childbirth.

    Time frame: baseline

Secondary outcomes

  1. Blood glucose self-monitoring

    control of diabetes by expected blood glucose targets

    Time frame: until birth (up to a maximum of 16 weeks)

  2. weight gain

    Time frame: during pregnancy until birth (up to a maximum of 16 weeks)

  3. type of birth

    Mode of parturition : Cesarean section or vaginal birth

    Time frame: baseline

  4. Measure of abdominal diameter

    Fetal Macrosomia suspected during fetal ultrasonography

    Time frame: before childbirth

  5. Measure of fetal weight

    Fetal Macrosomia suspected during fetal ultrasonography

    Time frame: before childbirth

  6. Birth weight

    Time frame: at childbirth

  7. Apgar score

    Time frame: 1 minute and 5 minutes after birthchild

  8. Neonatal blood glucose measurement

    Number of neonatal hypoglycemia

    Time frame: during the first 48 hours after birth

07

Study locations

1 of 1 sites recruiting
  • Caen University Hospital
    Caen, 14033, France
    Recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 26, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02945540
Lead sponsor
University Hospital, Caen
Responsible party
Sponsor
First posted
Oct 26, 2016
Start date
Apr 2016
Primary completion
Apr 2017 (estimated)
Completion
Apr 2017 (estimated)
Last update
Oct 26, 2016

Study contacts

Lidwine TRONCY, MSc
Contact
troncy-l@chu-caen.fr
+33 2 31 06 30 23

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2016. You cannot join it, but the record below documents what was studied.

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