DiabetesFlex - Patient Involvement and Patient-reported Outcome Measures in Type 1 Diabetes

Sponsor
Annesofie Lunde Jensen (Other)
Overall Status
Completed
CT.gov ID
NCT03202732
Collaborator
(none)
344
1
2
34.5
10

Study Details

Study Description

Brief Summary

The aim of this study is to investigate the effect of the use of DiabetesFlex in diabetes care compared to standard care in relation to patient involvement and relevance for specific group of persons with T1DM.

The investigators hypothesize that the use of DiabetesFlex will lead to a higher degree of patient in-volvement, improved glycaemic control and a decrease in total number of consultations compared to standard care. Furthermore, the investigators aim to identify if a specific sub-population within the T1DM population will benefit significantly from the intervention.

Condition or Disease Intervention/Treatment Phase
  • Other: DiabetesFlex
N/A

Detailed Description

Diabetes Mellitus (DM) is a chronic condition, and provision of individual and effective diabetes care is a major challenge. The is a lack of evidence on the optimal frequency of attending outpatient clinics for persons with T1DM.

The use of patient-reported outcome (PRO) measures in diabetes care area are limited and none existing in a Danish context. This includes studies, which combine PRO measure with diabetes management, patient involvement and self-management.

The study will generate knowledge and directions for ways to reframe and to optimize the future management of diabetes care.

Study Design

Study Type:
Interventional
Actual Enrollment :
344 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
DiabetesFlex - Patient Involvement and Patient-reported Outcome Measures in Type 1 Diabetes: A Randomised Controlled Trial and Interview Study
Actual Study Start Date :
Oct 9, 2017
Actual Primary Completion Date :
Aug 20, 2020
Actual Study Completion Date :
Aug 25, 2020

Arms and Interventions

Arm Intervention/Treatment
Other: DiabetesFlex

In DiabetesFlex intervention, patients are offered 3 consultations/year. One mandatory consultations (30 minutes). The patient, an endocrinologist and a diabetes nurse attend. Two optional consultations, patients can choose between face-to-face consultations, a telephone consultation or to cancel the consultation. Ahead of the consultations, patients fill out the AmbuFlex Diabetes questionnaire and deliver a blood and urine sample. Based on the patient's response to the AmbuFlex Diabetes questionnaire, the result of the blood sample and the urine sample, the diabetes nurse assign the patient to a face-to-face consultation, a telephone consultation or no consultation with an endocrinologist, a diabetes nurse or a dietician.

Other: DiabetesFlex
DiabetesFlex consist of one mandatory and two optional consultations. Before the consultations patients receive the AmbuFlex Diabetes questionnaire. The AmbuFlex Diabetes questionnaire is based on both validated questionnaires and clinical consensus. The AmbuFlex Diabetes questionnaire consists of: SF36 well-being question, WHO-5 Well-being Index. Questions concerning: HgA1c, home-based blood pressure monitoring, incidents of hypoglycemia, diabetes complications, regular eye check, regular food check, erectile dysfunction and peripheral neuropathy, The PAID scale, Topics patients may want to talk with the health care professional about, the patient's evaluation of the need for diabetes care. View the AmbuFlex Diabetes questionnaire at the homepage: www.diabetesflex.auh.dk.

No Intervention: Standard care

Standard diabetes care consists of 3 consultations (15 minutes)/year with a physician or a diabetes nurse by turns. Ahead of the consultation patients send in a blood sample for measuring HgA1c, urine sample for measuring urin-albumin creatinin ratio and other blood samples depending of arrangements made in the last consultation. Once a year in relation to a consultation, patients fill in the Problem Area In Diabetes (PAID) (20) scale together. Furthermore, based on the patients or healthcare professional judgement, patients see a dietician when needed.

Outcome Measures

Primary Outcome Measures

  1. HbA1c [15 mounth]

    Non-inferiority with respect to HbA1c

Secondary Outcome Measures

  1. General health will be assessed by items from the SF-36 questionnaire [15 mounth]

    General health will be measured at baseline and after 15 mounth

  2. Health literacy will be assessed by The Health Literacy Questionnaire (sub scale 6 and 9) [15 mounth]

    Health literacy will be measured at baseline and after 15 months.

  3. Well-being will be assessed by the WHO-5 Well-being Index [15 mounth]

    Well-being will be measured at baseline and after 15 months.

  4. Patient Activated Measure (PAM) [15 mounth]

    Patient Activated Measure (PAM) will be measured at baseline and after 15 months.

  5. "Generic questions concerning patient involvement" is validate by "DEFACTUM" [15 mounth]

    Patient involvement will be measured at baseline and after 15 months.

  6. The problem Areas In Diabetes Scale (PAID) [15 mounth]

    PAID will be measured at baseline and after 15 months.

  7. Blood pressure [15 mounth]

    Blood pressure will be measured at baseline and after 15 months.

  8. Urine albumine/creatinine ratio [15 mounth]

    urine albumine/creatinine ratio will be measured at baseline and after 15 months.

  9. Number and type consultations [15 mounth]

    Consultations consists of face-to-face, telephone, cancel, registered non-attendance and health care professional involved in the consultation will be measured after 15 mounth

  10. Mortality [15 mounth]

    Mortality will be measured after 15 months.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Age over 18 years Have had T1DM for more than 1 years Be able to use the Danish-language general website on healthcare www.sundhed.dk Be mentally well functioning Understand and read Danish Access to internet

Contacts and Locations

Locations

Site City State Country Postal Code
1 Aahurs University Hospital Aarhus Denmark 8000

Sponsors and Collaborators

  • Annesofie Lunde Jensen

Investigators

  • Principal Investigator: Annesofie L. Jensen, Postdoc, Aarhus University Hospital

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Annesofie Lunde Jensen, Clinical nursespecialist postdoc, Aarhus University Hospital
ClinicalTrials.gov Identifier:
NCT03202732
Other Study ID Numbers:
  • DiabetesFlex2017
First Posted:
Jun 29, 2017
Last Update Posted:
Nov 6, 2020
Last Verified:
Nov 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Annesofie Lunde Jensen, Clinical nursespecialist postdoc, Aarhus University Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 6, 2020