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CompletedNCT02076555PRIMO_SocialUpdated Aug 9, 2019

Diabetes and Social Issues: Evaluation of a Diabetes Education Module

An interventional study of Education - Diabetes and Social Issues in Diabetes Mellitus, sponsored by Forschungsinstitut der Diabetes Akademie Mergentheim. Completed at 4 sites in Germany. Open to participants aged 18 Years to 80 Years. Per ClinicalTrials.gov, last updated 2019-08-09.

Sponsored by Forschungsinstitut der Diabetes Akademie Mergentheim · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
256
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

This study is a multi-center, randomized prospective trial with a 6-month follow up. A newly developed treatment and education module will be tested compared to a waiting-list control group. The module covers the topic "diabetes and social issues". Primary outcome variable is diabetes-specific empowerment regarding diabetes and social issues. Secondary outcome variables are: diabetes-related distress, health-related quality of life, depressive symptoms, self-care behavior, and glycemic control.

Read the detailed description

The module consists of one lesson (duration: 90 minutes). The module is derived from the empowerment approach and is based on the previously evaluated education and treatment program for type 1 diabetes: PRIMAS (NCT01220557). The module is designed as a group session held by a trained diabetes educator. Patients are randomized either to the immediate participation in the module or to the control group. Control group is a waiting-list control group. Patients in this waiting-list control group get the education after the completion of the 6-month follow-up.

02

Conditions studied

  • Diabetes Mellitus

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Keywords

  • diabetes
  • education
  • randomized
  • prospective
03

In context

Diabetes Mellitus

10,925 studies on the registry are indexed under Diabetes Mellitus; 1,319 are open to participants now.

This study's enrollment of 256 is above the median of 80 across 8,367 interventional studies indexed under Diabetes Mellitus.

Browse Diabetes Mellitus studies →

Lead sponsor

Forschungsinstitut der Diabetes Akademie Mergentheim is the lead sponsor of 14 studies on the registry; 1 is open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Intensive insulin treatment
  • specific interest in "Diabetes and Social Issues"
  • wish to participate in group education
  • informed consent
  • fluent in reading and speaking German language

Exclusion criteria

Exclusion Criteria:

  • diabetes duration \< 4 week
  • severe organic disease (e.g. terminal renal disease, cancer with poor prognosis)
  • current treatment of a mental disease
  • cognitive impairment
  • dementia
  • pregnancy
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
256 participants (actual)

Study arms

  • Experimental
    Education - Diabetes and Social Issues

    Patients randomized to this arm, will participate immediately in the education module "Diabetes and Social Issues"

    Behavioral: Education - Diabetes and Social Issues

  • No intervention
    Waiting-list control group

    Patients in the control group will get the education with the education module after completion of the 6-month follow-up

Interventions

  • BehavioralEducation - Diabetes and Social Issues

    Based on the treatment and education programme PRIMAS a problem-specific education module regarding "Diabetes and Social Issues" was created. The module covers specific and detailed aspects of the topic "social issues" such as driver licence, hypoglycemia when driving, and the pass for severly handicapped persons. With this module, a more comprehensive education of patients with specific interest is possible.

06

What researchers measure

Primary outcomes

  1. Change from baseline in diabetes-specific empowerment on the adapted Diabetes Empowerment Scale at the 2-week and 6-month follow-up

    The Diabetes Empowerment Scale was specifically adjusted to cover the topic "social issues". Psychometric criteria for these adjusted scale were evaluated in an independent study

    Time frame: Baseline, 2-week follow-up , 6-month follow-up

Secondary outcomes

  1. Change from baseline in problem-specific distress on the adapted Problem Areas in Diabetes (PAID) Scale at the 2-week and 6-month follow-up

    The PAID scale was specifically adapted to cover the topic "social issues". Psychometric quality was assessed in an independent study

    Time frame: baseline, 2-week follow-up, 6-month follow-up

  2. Change from baseline in glycemic control (HbA1c) at the 2-week and 6-month follow-up

    HbA1c will be analyzed in a central laboratory.

    Time frame: baseline, 2-week follow-up, 6-month follow-up

  3. Change from baseline in health-related quality of life on the EQ-5D at the 2-week and 6-month follow-up

    Time frame: baseline, 2-week follow-up, 6-month follow-up

  4. Change from baseline in quality of life on the WHO-5 at the 2-week and 6-month follow-up

    Time frame: baseline, 2-week follow-up, 6-month follow-up

  5. Change from baseline in self-efficacy on the General Self-Efficacy Scale (GSE) the 2-week and 6-month follow-up

    Time frame: baseline, 2-week follow-up, 6-month follow-up

  6. Change from baseline in general diabetes-distress at the 2-week and 6-month follow-up

    Time frame: baseline, 2-week follow-up, 6-month follow-up

  7. Change from baseline in depressive symptoms on the CES-D at the 2-week and 6-month follow-up

    Time frame: baseline, 2-week follow-up, 6-month follow-up

07

Study locations

4 sites
  • Research Institute of the Diabetes Academy Mergentheim (FIDAM)
    Bad Mergentheim, 97980, Germany
  • Zentrum für Diabetologie Bergedorf
    Hamburg, 21029, Germany
  • Diabeteszentrum Ludwigsburg
    Ludwigsburg, 71634, Germany
  • Diabetologische Schwerpunktpraxis Neuss
    Neuss, 41462, Germany
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 9, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02076555
Lead sponsor
Forschungsinstitut der Diabetes Akademie Mergentheim
Responsible party
Norbert Hermanns (Head of the Research Institut Diabetes Academy Mergentheim, Forschungsinstitut der Diabetes Akademie Mergentheim) — Principal investigator
First posted
Mar 3, 2014
Start date
Feb 2014
Primary completion
Jan 2019
Completion
Jul 2019
Last update
Aug 9, 2019

Study contacts

Norbert Hermanns, PhD
principal investigator · Forschungsinstitut der Diabetes Akademie Mergentheim

Oversight

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

Not currently enrolling

This study is completed, as verified in Aug 2019. You cannot join it, but the record below documents what was studied.

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