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Evaluation of a Diabetes Treatment and Education Program for Insulin Pump Therapy (INPUT) (INPUT)

Primary Purpose

Diabetes Mellitus

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
INPUT
Sponsored by
Norbert Hermanns
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetes Mellitus focused on measuring self-management, empowerment, treatment and education program, insulin pump, diabetes education

Eligibility Criteria

16 Years - 75 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Existing insulin pump therapy
  • Prior participation in a structured diabetes education program
  • HbA1c ≥ 7,5% but ≤ 13%
  • Ability to understand, speak and write German language
  • informed consent (if necessary, informed consent of the parents)

Exclusion Criteria:

  • Diabetes duration < 1 year
  • severe organic disease preventing a regular participation in the training course
  • pregnancy
  • severe cognitive impairment
  • current treatment of psychiatric disorder
  • renal disease requiring dialysis

Sites / Locations

  • Diabetologische Schwerpunktpraxis Neuss

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

INPUT

Waiting list

Arm Description

INPUT consists of 12 lessons comprising all relevant information in order to treat diabetes with an insulin pump. Patients learn to effectively use the different features of their pump in order to improve not only glycemic control but also to improve the implementation of pump therapy in daily life. Psychological and motivational aspects of living with diabetes and living with an insulin pump are addressed as well.

Patients are randomly assigned to the waiting list. After completion of the 6-month follow-up, these patients will also receive training with INPUT.

Outcomes

Primary Outcome Measures

Changes in Glycemic Control Measured by A1c
Difference between baseline A1c and A1c at the 6-month follow-up

Secondary Outcome Measures

Hypoglycaemia Awareness
The hypoglycemia awareness questionnaire provides a score indicating the severity of hypoglycaemia unawareness. This scale ranges from 0 (maximum hypoglycaemia awareness) to 7 (minimum hypoglycaemia awareness), where a score of 4 suggests reduced hypoglycaemia awareness.
Diabetes Empowerment
Empowerment is measured by a German version of the Diabetes Empowerment Scale, a measure of diabetes-related psychosocial self-efficacy.
Satisfaction with current treatment
Satisfaction with current treatment is assessed via a 10-item scale. The total score ranges from 10 to 60 with lower scores indicating higher satisfaction.
Diabetes Self-Management
The Diabetes Self-Management Questionnaire is a self-report measure of patients' self-care. The level of self-care is assessed via Likert scales.
Diabetes Distress
The Diabetes Distress Scale (DDS) assesses diabetes-related stressors due to living and treating diabetes. Different aspects of distress are covered: emotional burden, physician-related, regimen-related, diabetes-related interpersonal
Problem Areas in Diabetes
The Problem Areas in Diabetes Scale (PAID) assesses the psychosocial adaptation to the burden of living with and treating diabetes.
Health-related Quality of Life
Health-related quality of life focuses on the health-specific aspects of quality of life and dealing with a chronic condition such as diabetes
Depressive symptoms
The presence and extent of typical depressive symptoms are assessed via self-report
Attitudes towards insulin pump therapy
Specific attitudes towards different aspects of insulin pump therapy are assessed via Likert scales. The questionnaire consists of 6 subscales that can be placed within 4 dimensions: (I) Expectations on insulin pump therapy (subscale: achieving better glycaemic control) (II) Perceived advantages of an insulin pump (subscale: gaining more flexibility) (III) Ease of use (subscales: design + functionality) (IV) Psychosocial effects and barriers (subscales: technological dependence + impaired body image)
Severe hypoglycaemia
The incidence of severe hypoglycaemia in the past six months is assessed via Case Report Forms. Severe hypoglycaemia is defined as requiring third party assistance or medical intervention for treating hypoglycaemia.

Full Information

First Posted
April 20, 2016
Last Updated
November 24, 2017
Sponsor
Norbert Hermanns
Collaborators
Berlin-Chemie
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1. Study Identification

Unique Protocol Identification Number
NCT02868931
Brief Title
Evaluation of a Diabetes Treatment and Education Program for Insulin Pump Therapy (INPUT)
Acronym
INPUT
Official Title
Evaluation of a Newly Developed Treatment and Education Program (INPUT) for Diabetic Patients Performing an Insulin Pump Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
November 2017
Overall Recruitment Status
Completed
Study Start Date
April 1, 2016 (Actual)
Primary Completion Date
February 2017 (Actual)
Study Completion Date
March 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Norbert Hermanns
Collaborators
Berlin-Chemie

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is a randomized, controlled, prospective trial with a 6-month follow-up. A newly developed treatment and education programme for diabetic patients with an insulin pump therapy (INPUT) will be tested compared to a waiting group. Primary outcome variable is the difference in glycemic control between baseline and the 6-month follow-up. Secondary outcome variables are: severe hypoglycaemia, diabetes-related distress, depressive symptoms, health-related quality of life, diabetes empowerment, self-care behavior, hypoglycemia awareness, and attitudes towards insulin pump therapy.
Detailed Description
INPUT is a self-management-based treatment and education program for diabetic patients with an insulin pump (CSII). It is designed to empower patients to adequately perform their therapy in daily life and to integrate their diabetes and their insulin pump into their lifes in order to enhance quality of life. INPUT ist tested in an randomized controlled trial (RCT) with a waiting-list control group since no certified and effective treatment and education program for CSII exists. This study is a multi-center study. Study centers are specialized diabetes practices throughout Germany. Patients will be approached by their respective practice and informed about the study. Study measurements as well as the conduct of INPUT will take place at the respective practice. Baseline measurement will take place 2 weeks prior to the beginning of INPUT. After completion of baseline measurement, all patients from one study center will be randomized centrally by the Research Institute of the Diabetes Academy Mergentheim (FIDAM). 2 weeks and 6 months after the completion of INPUT, follow-up measurements will be conducted at the respective study center. HbA1c as a marker of glycemic control will be analyzed in a central laboratory. Secondary outcome measures will be assessed via psychometrically tested questionnaires, Case Reports Forms, or patient files.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus
Keywords
self-management, empowerment, treatment and education program, insulin pump, diabetes education

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
268 (Actual)

8. Arms, Groups, and Interventions

Arm Title
INPUT
Arm Type
Experimental
Arm Description
INPUT consists of 12 lessons comprising all relevant information in order to treat diabetes with an insulin pump. Patients learn to effectively use the different features of their pump in order to improve not only glycemic control but also to improve the implementation of pump therapy in daily life. Psychological and motivational aspects of living with diabetes and living with an insulin pump are addressed as well.
Arm Title
Waiting list
Arm Type
No Intervention
Arm Description
Patients are randomly assigned to the waiting list. After completion of the 6-month follow-up, these patients will also receive training with INPUT.
Intervention Type
Behavioral
Intervention Name(s)
INPUT
Other Intervention Name(s)
treatment and education program for INsulin PUmp Therapy
Intervention Description
Treatment and education program based on the self-management theory of behavioral medicine. The program is delivered by certified and specially trained diabetes educators.
Primary Outcome Measure Information:
Title
Changes in Glycemic Control Measured by A1c
Description
Difference between baseline A1c and A1c at the 6-month follow-up
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Hypoglycaemia Awareness
Description
The hypoglycemia awareness questionnaire provides a score indicating the severity of hypoglycaemia unawareness. This scale ranges from 0 (maximum hypoglycaemia awareness) to 7 (minimum hypoglycaemia awareness), where a score of 4 suggests reduced hypoglycaemia awareness.
Time Frame
6 months
Title
Diabetes Empowerment
Description
Empowerment is measured by a German version of the Diabetes Empowerment Scale, a measure of diabetes-related psychosocial self-efficacy.
Time Frame
6 months
Title
Satisfaction with current treatment
Description
Satisfaction with current treatment is assessed via a 10-item scale. The total score ranges from 10 to 60 with lower scores indicating higher satisfaction.
Time Frame
6 months
Title
Diabetes Self-Management
Description
The Diabetes Self-Management Questionnaire is a self-report measure of patients' self-care. The level of self-care is assessed via Likert scales.
Time Frame
6 months
Title
Diabetes Distress
Description
The Diabetes Distress Scale (DDS) assesses diabetes-related stressors due to living and treating diabetes. Different aspects of distress are covered: emotional burden, physician-related, regimen-related, diabetes-related interpersonal
Time Frame
6 months
Title
Problem Areas in Diabetes
Description
The Problem Areas in Diabetes Scale (PAID) assesses the psychosocial adaptation to the burden of living with and treating diabetes.
Time Frame
6 months
Title
Health-related Quality of Life
Description
Health-related quality of life focuses on the health-specific aspects of quality of life and dealing with a chronic condition such as diabetes
Time Frame
6 months
Title
Depressive symptoms
Description
The presence and extent of typical depressive symptoms are assessed via self-report
Time Frame
6 months
Title
Attitudes towards insulin pump therapy
Description
Specific attitudes towards different aspects of insulin pump therapy are assessed via Likert scales. The questionnaire consists of 6 subscales that can be placed within 4 dimensions: (I) Expectations on insulin pump therapy (subscale: achieving better glycaemic control) (II) Perceived advantages of an insulin pump (subscale: gaining more flexibility) (III) Ease of use (subscales: design + functionality) (IV) Psychosocial effects and barriers (subscales: technological dependence + impaired body image)
Time Frame
6 months
Title
Severe hypoglycaemia
Description
The incidence of severe hypoglycaemia in the past six months is assessed via Case Report Forms. Severe hypoglycaemia is defined as requiring third party assistance or medical intervention for treating hypoglycaemia.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Existing insulin pump therapy Prior participation in a structured diabetes education program HbA1c ≥ 7,5% but ≤ 13% Ability to understand, speak and write German language informed consent (if necessary, informed consent of the parents) Exclusion Criteria: Diabetes duration < 1 year severe organic disease preventing a regular participation in the training course pregnancy severe cognitive impairment current treatment of psychiatric disorder renal disease requiring dialysis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Norbert Hermanns, PhD
Organizational Affiliation
Forschungsinstitut der Diabetes Akademie Mergentheim (FIDAM GmbH)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Diabetologische Schwerpunktpraxis Neuss
City
Neuss
ZIP/Postal Code
41462
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
30305343
Citation
Ehrmann D, Kulzer B, Schipfer M, Lippmann-Grob B, Haak T, Hermanns N. Efficacy of an Education Program for People With Diabetes and Insulin Pump Treatment (INPUT): Results From a Randomized Controlled Trial. Diabetes Care. 2018 Dec;41(12):2453-2462. doi: 10.2337/dc18-0917. Epub 2018 Oct 10.
Results Reference
derived

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Evaluation of a Diabetes Treatment and Education Program for Insulin Pump Therapy (INPUT)

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