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Tailored Support for Type 2 Diabetes Patients With an Acute Coronary Event After Discharge From Hospital (Diacourse)

Primary Purpose

Type 2 Diabetes, Acute Coronary Event

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Home visits
Consultation by telephone
Sponsored by
UMC Utrecht
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Type 2 Diabetes focused on measuring Type 2 diabetes, Acute Coronary Event (ACE), Distress, Self-efficacy, Quality of Life, Depression, Primary care, Illness representations

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • History of type 2 diabetes (>1 year)
  • Discharged from the hospital after a first acute coronary event defined as a Myocardial Infarction (MI), Coronary Artery Bypass Graft (CABG) procedure or Percutaneous Transluminal Coronary Angioplasty (PTCA)
  • Sufficient knowledge of the Dutch language

Exclusion Criteria:

  • A serious illness or condition which will prevent full participation
  • Not able to fill in questionnaires

Sites / Locations

  • Meander Medical Center
  • Gelre Hospitals
  • Lievensberg Hospital
  • Amphia Hospital
  • Gemini Hospital
  • Admiraal de Ruyter Hospital
  • Beatrix Hospital
  • Westfriesgasthuis
  • Sint Antonius Hospital
  • Canisius Wilhelmina Hospital
  • Diakonessenhuis
  • Sint Antonius Hospital
  • University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Home visits

Consultation by telephone

Arm Description

In addition to usual care the patients will receive three home visits from a trained diabetes nurse. The first visit (65 minutes) is within three weeks after discharge from the hospital; the second visit (45 minutes) is two weeks later and the third visit (45 minutes) is two months after the second home visit.

In addition to usual care patients will receive a consultation by telephone within three weeks after discharge to offer them personal attention. In this consultation they will get the opportunity to discuss in ten to fifteen minutes how they feel in the period after discharge.

Outcomes

Primary Outcome Measures

Change in Diabetes related distress
Diabetes related distress measure with the Problem Areas in Diabetes (PAID) questionnaire. The PAID is a Self-reported questionnaire consisting of twenty statements identified as common negative emotions related to living with diabetes. Each item is rated on a 5-point Likert scale, ranging from 0 ("not a problem") to 4 ("a serious problem"). The total score is transformed to a 0-100 scale, with higher score representing higher distress.

Secondary Outcome Measures

Change in Well-being
Measured with the WHO-Five Well-being Index (WHO-5). The five items covering positive mood (good spirits, relaxation), vitality (being active and waking up fresh and rested), and general interests (being interested in things) in the past two weeks
Change in Quality of life
Euroqol 5 Dimensions (EQ-5D) and the Euroqol Visual Scale (EQ-VAS). The EQ-5D measures general health status on five dimensions: Mobility Self-care Usual activities Pain/discomfort Anxiety/depression The EQ-VAS measures the overall health state on a graded, vertical line.
Change in Anxiety and depression
Measured with the Hospital Anxiety and Depression Scale (HADS). A questionnaire measuring anxiety (7 items) and depression (7 items).
Change in Physical activity
Measured with the International Physical Activity Questionnaire (IPAQ). 29 Items measure how many days' physical activities are performed during the past seven days in four domains (work, transportation, housework and leisure-time).
Change in Self care
Measured with the Summary of the Diabetes Self-Care Activities Measure (SDSCA). Eleven items assessing several aspects of the diabetes regimen: general diet, specific diet, exercise, blood glucose testing, foot care, and smoking. Items measure how many days a patient has performed self-care activities in the last seven days.
Change in Diabetes coping
Measured with the Diabetes Coping Measure (DCM) consisting of four scales measuring diabetes coping: tackling spirit, avoidance, passive resignation and diabetes integration.
Change in Biomedical variables
Blood pressure, blood lipids (total cholesterol, HDL cholesterol, LDL cholesterol and triglycerides) and body mass index

Full Information

First Posted
February 14, 2013
Last Updated
July 25, 2014
Sponsor
UMC Utrecht
Collaborators
Dutch Diabetes Research Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT01801631
Brief Title
Tailored Support for Type 2 Diabetes Patients With an Acute Coronary Event After Discharge From Hospital
Acronym
Diacourse
Official Title
Tailored Support for Type 2 Diabetes Patients With an Acute Coronary Event After Discharge From Hospital
Study Type
Interventional

2. Study Status

Record Verification Date
July 2014
Overall Recruitment Status
Completed
Study Start Date
October 2011 (undefined)
Primary Completion Date
December 2013 (Actual)
Study Completion Date
December 2013 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
UMC Utrecht
Collaborators
Dutch Diabetes Research Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Background: In type 2 diabetes mellitus patients, an acute coronary event (ACE) may result in a decreased quality of life and increased distress. According to the American Diabetes Association, transition from the acute care setting is a high-risk time for all patients, but tailored support specific to diabetes is scarce in that period. The investigators developed an intervention by a diabetes nurse to help diabetic patients reduce distress after their first ACE. The intervention is based on Bandura's Social Cognitive Theory, Leventhal's Common Sense Model, and on results of focus groups which were conducted to define the needs and wishes of type 2 diabetes patients and their partners regarding professional support after an ACE. The aim of this study is to evaluate the effectiveness of the intervention to reduce distress. The hypothesis is that patients who receive the intervention will have less diabetes related distress compared to the control group. Methods/Design: Randomized controlled trial. Patients will be recruited directly after discharge from hospital. A diabetes nurse will visit the patients in the intervention group (n = 100) within three weeks after discharge from hospital, two weeks later and two months later. The control group (n = 100) will receive a telephone consultation. The primary outcome is diabetes related distress, measured with the Problem Areas in Diabetes questionnaire (PAID). Secondary outcomes are quality of life, anxiety, depression, HbA1c, blood pressure and lipids. Mediating variables are self-management, self-efficacy and illness representations. Variables will be measured with questionnaires directly after discharge from hospital and five months later. Biomedical variables will be obtained from the records from the primary care physician and the hospital. Differences between groups in change over time will be analyzed according to the intention-to-treat principle. Discussion: Type 2 diabetes patients who experience a first ACE need tailored support after discharge from the hospital. This trial will provide evidence of the effectiveness of a supportive intervention to reduce distress in these patients.
Detailed Description
See citation design paper

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes, Acute Coronary Event
Keywords
Type 2 diabetes, Acute Coronary Event (ACE), Distress, Self-efficacy, Quality of Life, Depression, Primary care, Illness representations

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Home visits
Arm Type
Experimental
Arm Description
In addition to usual care the patients will receive three home visits from a trained diabetes nurse. The first visit (65 minutes) is within three weeks after discharge from the hospital; the second visit (45 minutes) is two weeks later and the third visit (45 minutes) is two months after the second home visit.
Arm Title
Consultation by telephone
Arm Type
Other
Arm Description
In addition to usual care patients will receive a consultation by telephone within three weeks after discharge to offer them personal attention. In this consultation they will get the opportunity to discuss in ten to fifteen minutes how they feel in the period after discharge.
Intervention Type
Other
Intervention Name(s)
Home visits
Intervention Description
In addition to usual care the patients will receive three home visits from a trained diabetes nurse. The first visit (65 minutes) is within three weeks after discharge from the hospital; the second visit (45 minutes) is two weeks later and the third visit (45 minutes) is two months after the second home visit.
Intervention Type
Other
Intervention Name(s)
Consultation by telephone
Intervention Description
In addition to usual care patients will receive a consultation by telephone within three weeks after discharge to offer them personal attention. In this consultation they will get the opportunity to discuss in ten to fifteen minutes how they feel in the period after discharge.
Primary Outcome Measure Information:
Title
Change in Diabetes related distress
Description
Diabetes related distress measure with the Problem Areas in Diabetes (PAID) questionnaire. The PAID is a Self-reported questionnaire consisting of twenty statements identified as common negative emotions related to living with diabetes. Each item is rated on a 5-point Likert scale, ranging from 0 ("not a problem") to 4 ("a serious problem"). The total score is transformed to a 0-100 scale, with higher score representing higher distress.
Time Frame
At 2 weeks and 5 months after discharge from hospital
Secondary Outcome Measure Information:
Title
Change in Well-being
Description
Measured with the WHO-Five Well-being Index (WHO-5). The five items covering positive mood (good spirits, relaxation), vitality (being active and waking up fresh and rested), and general interests (being interested in things) in the past two weeks
Time Frame
At 2 weeks and 5 months after discharge from hospital
Title
Change in Quality of life
Description
Euroqol 5 Dimensions (EQ-5D) and the Euroqol Visual Scale (EQ-VAS). The EQ-5D measures general health status on five dimensions: Mobility Self-care Usual activities Pain/discomfort Anxiety/depression The EQ-VAS measures the overall health state on a graded, vertical line.
Time Frame
At 2 weeks and 5 months after discharge from hospital
Title
Change in Anxiety and depression
Description
Measured with the Hospital Anxiety and Depression Scale (HADS). A questionnaire measuring anxiety (7 items) and depression (7 items).
Time Frame
At 2 weeks and 5 months after discharge from hospital
Title
Change in Physical activity
Description
Measured with the International Physical Activity Questionnaire (IPAQ). 29 Items measure how many days' physical activities are performed during the past seven days in four domains (work, transportation, housework and leisure-time).
Time Frame
At 2 weeks and 5 months after discharge from hospital
Title
Change in Self care
Description
Measured with the Summary of the Diabetes Self-Care Activities Measure (SDSCA). Eleven items assessing several aspects of the diabetes regimen: general diet, specific diet, exercise, blood glucose testing, foot care, and smoking. Items measure how many days a patient has performed self-care activities in the last seven days.
Time Frame
At 2 weeks and 5 months after discharge from hospital
Title
Change in Diabetes coping
Description
Measured with the Diabetes Coping Measure (DCM) consisting of four scales measuring diabetes coping: tackling spirit, avoidance, passive resignation and diabetes integration.
Time Frame
At 2 weeks and 5 months after discharge from hospital
Title
Change in Biomedical variables
Description
Blood pressure, blood lipids (total cholesterol, HDL cholesterol, LDL cholesterol and triglycerides) and body mass index
Time Frame
At 2 weeks and 5 months after discharge from hospital
Other Pre-specified Outcome Measures:
Title
Change in Self-efficacy
Description
Measured with the Confidence in Diabetes Self-care questionnaire consisting of 20 items measuring diabetes specific self-efficacy.
Time Frame
At 2 weeks and 5 months after discharge from hospital
Title
Change in Illness perceptions
Description
Measured with the Illness Perception Questionnaire (IPQ) - short version. Questionnaire assessing the cognitive representation of illness, focuses on seven scales, assessing (1) Timeline acute/chronic and (2) Timeline cyclical (3) Consequences (4) Personal control (5) Treatment control (6) Illness coherence (7) Emotional representation
Time Frame
At 2 weeks and 5 months after discharge from hospital
Title
Change in Spousal support
Description
Measured with the Active Engagement, Protective Buffering and Overprotection (ABO) questionnaire. Five items measure active engagement, eight items measure protective buffering and six items measure overprotection
Time Frame
At 2 weeks and 5 months after discharge from hospital

10. Eligibility

Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: History of type 2 diabetes (>1 year) Discharged from the hospital after a first acute coronary event defined as a Myocardial Infarction (MI), Coronary Artery Bypass Graft (CABG) procedure or Percutaneous Transluminal Coronary Angioplasty (PTCA) Sufficient knowledge of the Dutch language Exclusion Criteria: A serious illness or condition which will prevent full participation Not able to fill in questionnaires
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guy E. Rutten, Professor
Organizational Affiliation
UMC Utrecht
Official's Role
Principal Investigator
Facility Information:
Facility Name
Meander Medical Center
City
Amersfoort
Country
Netherlands
Facility Name
Gelre Hospitals
City
Apeldoorn
Country
Netherlands
Facility Name
Lievensberg Hospital
City
Bergen op Zoom
Country
Netherlands
Facility Name
Amphia Hospital
City
Breda
Country
Netherlands
Facility Name
Gemini Hospital
City
Den Helder
Country
Netherlands
Facility Name
Admiraal de Ruyter Hospital
City
Goes
Country
Netherlands
Facility Name
Beatrix Hospital
City
Gorinchem
Country
Netherlands
Facility Name
Westfriesgasthuis
City
Hoorn
Country
Netherlands
Facility Name
Sint Antonius Hospital
City
Nieuwegein
Country
Netherlands
Facility Name
Canisius Wilhelmina Hospital
City
Nijmegen
Country
Netherlands
Facility Name
Diakonessenhuis
City
Utrecht
Country
Netherlands
Facility Name
Sint Antonius Hospital
City
Utrecht
Country
Netherlands
Facility Name
University Medical Center
City
Utrecht
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
24438342
Citation
Kasteleyn MJ, Gorter KJ, Stellato RK, Rijken M, Nijpels G, Rutten GE. Tailored support for type 2 diabetes patients with an acute coronary event after discharge from hospital - design and development of a randomised controlled trial. Diabetol Metab Syndr. 2014 Jan 18;6(1):5. doi: 10.1186/1758-5996-6-5.
Results Reference
background
PubMed Identifier
24389352
Citation
Kasteleyn MJ, Gorter KJ, van Puffelen AL, Heijmans M, Vos RC, Jansen H, Rutten GE. What follow-up care and self-management support do patients with type 2 diabetes want after their first acute coronary event? A qualitative study. Prim Care Diabetes. 2014 Oct;8(3):195-206. doi: 10.1016/j.pcd.2013.12.001. Epub 2014 Jan 3.
Results Reference
background

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Tailored Support for Type 2 Diabetes Patients With an Acute Coronary Event After Discharge From Hospital

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