search
Back to results

Improving Glycaemic Control in Patients With Type 2 Diabetes Mellitus Through Peer Support Instant Messaging (DiabPeerS)

Primary Purpose

Diabetes Mellitus, Type 2, Peer Support, Instant Messaging Service

Status
Enrolling by invitation
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
Peer Support Intervention via Instant Messaging Service Tool (IMS-Tool)
antidiabetic therapy according to the current guidelines
Sponsored by
St. Pölten University of Applied Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Diabetes Mellitus, Type 2 focused on measuring Diabetes Mellitus Type 2, Online Intervention, Peer Support, Instant Messaging Service, Glycaemic Control

Eligibility Criteria

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

Inclusion criteria participants exclusive moderators:

  • diagnosed type 2 diabetes mellitus according to the Austrian definition
  • HbA1c of ≥ 6.5% (48 mmol/mol) at the last measurement
  • receive the antidiabetic therapy according to the current guidelines
  • older than 40 years
  • living in Lower Austria
  • get oral hyperglycaemic agents for maximum three years
  • understand the individual commitments during trial
  • must be able to visit training and measurements

Inclusion criteria moderators:

  • diagnosed type 2 diabetes mellitus according to the Austrian definition
  • HbA1c of ≥ 6.5% (48 mmol/mol) at the last measurement
  • receive the antidiabetic therapy according to the current guidelines
  • get oral hyperglycaemic agents for three years minimum
  • older than 60 years
  • living in the vicinity of the training location in St. Pölten, which means residing in St. Pölten, St. Pölten Land, Melk, Krems, or Lilienfeld
  • engaged participating (= regular participation) in the Austrian disease management program 'Therapie aktiv - Diabetes im Griff'
  • understand the individual commitments during trial
  • must be able to visit training and measurements
  • commitment to undergo the moderator training

Exclusion Criteria for all participants:

  • hospitalization of more than 3 weeks during the intervention
  • eye disorders that severely limit vision and, hence, inability to read the display (e.g., proliferative retinopathy or macular edema)
  • severe illnesses such as kidney, liver, heart disease, or malignant cancer, neurological of mental illness which make a longer hospitalization likely
  • substance abuse
  • pregnancy
  • limitation in the German language
  • unable to visit training and measurements

Sites / Locations

  • Sankt Pölten University of Applied Sciences

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

intervention group

control group

Arm Description

The intervention group will receive antidiabetic therapy according to the current guidelines but with the additional opportunity to use the peer support IMS tool. Peer support and moderation of the intervention group will be provided by moderators. Moderators will be supervised by a dietitian.

The control group receives the antidiabetic therapy according to the current guidelines, but without having access to the IMS tool. This means that participants receive medical treatment by their practitioner according to the Austrian recommendations.

Outcomes

Primary Outcome Measures

HbA1c [%] (change over a period of 7 months intervention and 7 months follow-up with 4 measurement dates)
HbA1c = glycated haemoglobin reflects average plasma glucose over the previous 8-12 weeks. It can be tested at any time of the day and does not require special preparation like fasting

Secondary Outcome Measures

Quality of life measured by Short-Form-Health Survey (SF-12) (change over a period of 7 months intervention and 7 months follow-up with 4 measurement dates)
Quality of life will be measured using the 'Short-Form-Health Survey' (SF-12): the SF-12 includes eight dimensions ('physical functioning', 'role limitations due to physical problems', 'bodily pain', 'vitality', 'general health perceptions' , 'social functioning', 'role limitations due to emotional problems', 'mental health'). The summary scores 'physical component summary' and 'mental component summary' (0-100 scales) can be calculated from the specified scales.
Medication adherence measured by A-14 (change over a period of 7 months intervention and 7 months follow-up with 4 measurement dates)
Medication adherence will be measured using the 'A14-scale': the A14 consists of 14 items of non-adherent behaviors phrased in a non-threatening and non-judgemental way using a five-item Likert scale with the endpoints '4' (never) to '0' (very often).
Diabetes self-management behaviors measured by 'Summary of Diabetes Self-Care Activities German' (SDSCA-G) (change over a period of 7 months intervention and 7 months follow-up with 4 measurement dates)
Diabetes self-management behaviors will be measured using the 'Summary of Diabetes Self-Care Activities German' (SDSCA-G): the SDSCA-G focuses on the past seven days related to the diabetes self-care activities 'nutrition', 'physical activities', 'blood glucose testing', 'foot care', and 'smoking'.
Diabetes knowledge will be measured using the 'Diabetes Knowledge Test' (DKT)
DKT consists of 20 statements about diabetes which have to be rated as 'true', 'false' or 'don't know'. Based on the answers, a difficulty index (percent of patients who scored correctly) is calculated.
Diabetes distress will be measure using the 'Diabetes Distress Scale' (DDS)
the DDS includes for dimensions of distress ('emotional burden', 'regimen distress', 'interpersonal distress', 'physician distress'). The DDS consists of 17 items using a six-point Likert scale with the endpoints '1' (not a problem) and '5' (a very serious problem).
Depression will be measured using the 'Patient Health Questionnaire-9' (PHQ-9)
PHQ-9 asks for all nine criteria of depression as defined in the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) using a four-point Likert scale with the endpoints '0' (not at all) and '3' (nearly every day).
Social support will be measured using the 'Fragebogen zur Sozialen Unterstützung' (F-SozU)
F-SozU operationalizes social support as perceived or anticipated support from the social environment. The short form consists of the following subscales: 'emotional support', 'practical support', 'social integration', 'stress from the social network'. The F-SozU involves of 14 items using a five-point Likert scale with the endpoints '1' (does not apply) and '5' (accurate).
Dietary behaviour will be measured using a Food Frequency Questionnaire
Asses the dietary behaviour during the last month
Physical activity will be measured using the 'International Physical Activity Questionnaire Short Form' (IPAQ-SF)
IPAQ-SF asks seven questions to assess 'vigorous-intensity' and 'moderate-intensity' physical activity as well as 'walking' and 'sitting'. Participants indicate the time in minutes or hours for each activity level. Based on this information, three levels of physical activity (low, moderate, high) are calculated and expressed in metabolic equivalent of task (MET) minutes per week.
Biochemical parameters
fasting blood glucose [mg/dl], total cholesterol [mg/dl], high-density lipoprotein [mg/dl], low-density lipoprotein [mg/dl], blood pressurge [mmHg], body height [cm], body weight [cm], body fat [%]

Full Information

First Posted
March 9, 2021
Last Updated
April 20, 2022
Sponsor
St. Pölten University of Applied Sciences
Collaborators
Karl Landsteiner University of Health Sciences, Austrian Health Insurance Fund
search

1. Study Identification

Unique Protocol Identification Number
NCT04797429
Brief Title
Improving Glycaemic Control in Patients With Type 2 Diabetes Mellitus Through Peer Support Instant Messaging
Acronym
DiabPeerS
Official Title
Improving Glycaemic Control in Patients With Type 2 Diabetes Mellitus Through Peer Support Instant Messaging: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Enrolling by invitation
Study Start Date
November 1, 2020 (Actual)
Primary Completion Date
November 2023 (Anticipated)
Study Completion Date
April 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
St. Pölten University of Applied Sciences
Collaborators
Karl Landsteiner University of Health Sciences, Austrian Health Insurance Fund

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Diabetes mellitus is one of the four priority non-communicable diseases worldwide. Globally, 425 million adults suffered from diabetes mellitus (7.2-11.3%) in 2017 and the International Diabetes Federation estimates an increase of 48% of the prevalence until 2045. Type 2 diabetes, which is the most common type of diabetes, is mainly seen in adults older than 40 years. Diabetes can lead to serious long-term complications as well as a lower quality of life, worse mental health, and a reduced life expectancy. Due to the chronical character of diabetes, the disease requires continuous therapy, regular medical appointments, and good adherence of those suffering. Therefore, diabetes self-management education (DSME) plays a significant role to increase patient's self-management capacity and improve diabetes therapy. Research indicates that these outcomes might be difficult to maintain and seem to decline soon after DSME ends. Consequently, effective strategies to preserve the positive effects of DSME are needed. Preliminary results show that peer support, which means support from a person who has experiential knowledge of a specific behaviour or stressor and similar characteristics as the target population, is associated with better outcomes in terms of HbA1c, cardiovascular disease risk factors or self-efficacy at lower cost compared to standard therapy. Although those results are promising, research on peer support in diabetes care is still in its infancy and the influence of various factors is unclear. Peer support instant messaging services (IMS) approaches have significant potential for diabetes management because support can be provided easily and prompt, is inexpensive, and needs less effort to attend compared to standard therapy. Furthermore, almost half of the 40-69-year-old age group, which is mostly affected by the onset of type 2 diabetes, use IMS. The major objective of the project is to analyse the impact of a peer supported IMS intervention in addition to a standard diabetes therapy on the glycaemic control of type 2 diabetic patients. A total of 205 participants (196 participants and 9 moderators) with type 2 diabetes mellitus, older than 40 years will be included and randomly assigned to the intervention or control group. Both groups will receive standard therapy, but the intervention group will use the peer support IMS tool, additionally. The duration of the intervention will last for seven months, followed by a follow-up of seven months. Biochemical, behavioural, and psychosocial parameters will be measured before, in the middle, and after the intervention as well as after the follow-up.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes Mellitus, Type 2, Peer Support, Instant Messaging Service
Keywords
Diabetes Mellitus Type 2, Online Intervention, Peer Support, Instant Messaging Service, Glycaemic Control

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Masking Description
blinding is not possible because of obvious differences between the interventions: the intervention group participates in the IMS-intervention and the control group does not
Allocation
Randomized
Enrollment
205 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
intervention group
Arm Type
Experimental
Arm Description
The intervention group will receive antidiabetic therapy according to the current guidelines but with the additional opportunity to use the peer support IMS tool. Peer support and moderation of the intervention group will be provided by moderators. Moderators will be supervised by a dietitian.
Arm Title
control group
Arm Type
Active Comparator
Arm Description
The control group receives the antidiabetic therapy according to the current guidelines, but without having access to the IMS tool. This means that participants receive medical treatment by their practitioner according to the Austrian recommendations.
Intervention Type
Other
Intervention Name(s)
Peer Support Intervention via Instant Messaging Service Tool (IMS-Tool)
Intervention Description
Peer Support via the IMS-tool increases diabetes self-management, improves self-efficiacy, adherence and glycaemic control
Intervention Type
Other
Intervention Name(s)
antidiabetic therapy according to the current guidelines
Intervention Description
In contrast, the control group has to manage their diabetes mellitus type 2 with standard support and without online exchange.
Primary Outcome Measure Information:
Title
HbA1c [%] (change over a period of 7 months intervention and 7 months follow-up with 4 measurement dates)
Description
HbA1c = glycated haemoglobin reflects average plasma glucose over the previous 8-12 weeks. It can be tested at any time of the day and does not require special preparation like fasting
Time Frame
at baseline, three months after the start of the intervention, at the end of the intervention = seven months after the start of the intervention, follow-up = 14 months after the start of the intervention
Secondary Outcome Measure Information:
Title
Quality of life measured by Short-Form-Health Survey (SF-12) (change over a period of 7 months intervention and 7 months follow-up with 4 measurement dates)
Description
Quality of life will be measured using the 'Short-Form-Health Survey' (SF-12): the SF-12 includes eight dimensions ('physical functioning', 'role limitations due to physical problems', 'bodily pain', 'vitality', 'general health perceptions' , 'social functioning', 'role limitations due to emotional problems', 'mental health'). The summary scores 'physical component summary' and 'mental component summary' (0-100 scales) can be calculated from the specified scales.
Time Frame
at baseline, three months after the start of the intervention, at the end of the intervention = seven months after the start of the intervention, follow-up = 14 months after the start of the intervention
Title
Medication adherence measured by A-14 (change over a period of 7 months intervention and 7 months follow-up with 4 measurement dates)
Description
Medication adherence will be measured using the 'A14-scale': the A14 consists of 14 items of non-adherent behaviors phrased in a non-threatening and non-judgemental way using a five-item Likert scale with the endpoints '4' (never) to '0' (very often).
Time Frame
at baseline, three months after the start of the intervention, at the end of the intervention = seven months after the start of the intervention, follow-up = 14 months after the start of the intervention
Title
Diabetes self-management behaviors measured by 'Summary of Diabetes Self-Care Activities German' (SDSCA-G) (change over a period of 7 months intervention and 7 months follow-up with 4 measurement dates)
Description
Diabetes self-management behaviors will be measured using the 'Summary of Diabetes Self-Care Activities German' (SDSCA-G): the SDSCA-G focuses on the past seven days related to the diabetes self-care activities 'nutrition', 'physical activities', 'blood glucose testing', 'foot care', and 'smoking'.
Time Frame
at baseline, three months after the start of the intervention, at the end of the intervention = seven months after the start of the intervention, follow-up = 14 months after the start of the intervention
Title
Diabetes knowledge will be measured using the 'Diabetes Knowledge Test' (DKT)
Description
DKT consists of 20 statements about diabetes which have to be rated as 'true', 'false' or 'don't know'. Based on the answers, a difficulty index (percent of patients who scored correctly) is calculated.
Time Frame
at baseline, three months after the start of the intervention, at the end of the intervention = seven months after the start of the intervention, follow-up = 14 months after the start of the intervention
Title
Diabetes distress will be measure using the 'Diabetes Distress Scale' (DDS)
Description
the DDS includes for dimensions of distress ('emotional burden', 'regimen distress', 'interpersonal distress', 'physician distress'). The DDS consists of 17 items using a six-point Likert scale with the endpoints '1' (not a problem) and '5' (a very serious problem).
Time Frame
at baseline, three months after the start of the intervention, at the end of the intervention = seven months after the start of the intervention, follow-up = 14 months after the start of the intervention
Title
Depression will be measured using the 'Patient Health Questionnaire-9' (PHQ-9)
Description
PHQ-9 asks for all nine criteria of depression as defined in the Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) using a four-point Likert scale with the endpoints '0' (not at all) and '3' (nearly every day).
Time Frame
at baseline, three months after the start of the intervention, at the end of the intervention = seven months after the start of the intervention, follow-up = 14 months after the start of the intervention
Title
Social support will be measured using the 'Fragebogen zur Sozialen Unterstützung' (F-SozU)
Description
F-SozU operationalizes social support as perceived or anticipated support from the social environment. The short form consists of the following subscales: 'emotional support', 'practical support', 'social integration', 'stress from the social network'. The F-SozU involves of 14 items using a five-point Likert scale with the endpoints '1' (does not apply) and '5' (accurate).
Time Frame
at baseline, three months after the start of the intervention, at the end of the intervention = seven months after the start of the intervention, follow-up = 14 months after the start of the intervention
Title
Dietary behaviour will be measured using a Food Frequency Questionnaire
Description
Asses the dietary behaviour during the last month
Time Frame
at baseline, three months after the start of the intervention, at the end of the intervention = seven months after the start of the intervention, follow-up = 14 months after the start of the intervention
Title
Physical activity will be measured using the 'International Physical Activity Questionnaire Short Form' (IPAQ-SF)
Description
IPAQ-SF asks seven questions to assess 'vigorous-intensity' and 'moderate-intensity' physical activity as well as 'walking' and 'sitting'. Participants indicate the time in minutes or hours for each activity level. Based on this information, three levels of physical activity (low, moderate, high) are calculated and expressed in metabolic equivalent of task (MET) minutes per week.
Time Frame
at baseline, three months after the start of the intervention, at the end of the intervention = seven months after the start of the intervention, follow-up = 14 months after the start of the intervention
Title
Biochemical parameters
Description
fasting blood glucose [mg/dl], total cholesterol [mg/dl], high-density lipoprotein [mg/dl], low-density lipoprotein [mg/dl], blood pressurge [mmHg], body height [cm], body weight [cm], body fat [%]
Time Frame
at baseline, three months after the start of the intervention, at the end of the intervention = seven months after the start of the intervention, follow-up = 14 months after the start of the intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria participants exclusive moderators: diagnosed type 2 diabetes mellitus according to the Austrian definition HbA1c of ≥ 6.5% (48 mmol/mol) at the last measurement receive the antidiabetic therapy according to the current guidelines older than 40 years living in Lower Austria get oral hyperglycaemic agents for maximum three years understand the individual commitments during trial must be able to visit training and measurements Inclusion criteria moderators: diagnosed type 2 diabetes mellitus according to the Austrian definition HbA1c of ≥ 6.5% (48 mmol/mol) at the last measurement receive the antidiabetic therapy according to the current guidelines get oral hyperglycaemic agents for three years minimum older than 60 years living in the vicinity of the training location in St. Pölten, which means residing in St. Pölten, St. Pölten Land, Melk, Krems, or Lilienfeld engaged participating (= regular participation) in the Austrian disease management program 'Therapie aktiv - Diabetes im Griff' understand the individual commitments during trial must be able to visit training and measurements commitment to undergo the moderator training Exclusion Criteria for all participants: hospitalization of more than 3 weeks during the intervention eye disorders that severely limit vision and, hence, inability to read the display (e.g., proliferative retinopathy or macular edema) severe illnesses such as kidney, liver, heart disease, or malignant cancer, neurological of mental illness which make a longer hospitalization likely substance abuse pregnancy limitation in the German language unable to visit training and measurements
Facility Information:
Facility Name
Sankt Pölten University of Applied Sciences
City
St. Pölten
State/Province
Lower Austria
ZIP/Postal Code
3100
Country
Austria

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
35422003
Citation
Hold E, Grublbauer J, Wiesholzer M, Wewerka-Kreimel D, Stieger S, Kuschei W, Kisser P, Gutzer E, Hemetek U, Ebner-Zarl A, Pripfl J. Improving glycemic control in patients with type 2 diabetes mellitus through a peer support instant messaging service intervention (DiabPeerS): study protocol for a randomized controlled trial. Trials. 2022 Apr 14;23(1):308. doi: 10.1186/s13063-022-06202-2.
Results Reference
derived

Learn more about this trial

Improving Glycaemic Control in Patients With Type 2 Diabetes Mellitus Through Peer Support Instant Messaging

We'll reach out to this number within 24 hrs