The Together on Diabetes Intervention - a Realist Evaluation

January 20, 2021 updated by: Stine Garn, Center for Diabetes, Copenhagen Municipality

The Together on Diabetes Intervention

The Danish healthcare system is universal and free of charge for Danish citizens, as all healthcare services are financed by general taxes. However, socioeconomic differences exist in access to healthcare services, treatment, and consequences of type 2-diabetes (T2D).

Using a realistic evaluation approach, this study aimed to evaluate the implementation of a Danish peer support intervention, targeted on improving self-management and use of healthcare services among socially vulnerable people with type 2-diabetes ("peers"). The study focused on the mechanisms generating the intended outcomes. Further, how contextual factors in peers' everyday life facilitated or hindered the mechanisms to operate.

The study design is a multi-method case study (n=9). Data include qualitative semi-structured interviews with four key groups of informants (peer, peer supporter, project manager, and a diabetes nurse). Each type of informant per case was interviewed (n=25) to obtain different perspectives of how the peers' interacted, and benefited from the intervention. All interviews were completed immediately after the after the 6-month intervention.

Further, a quantitative survey was conducted among peers at baseline (N=9) and follow-up (N=9) to obtain information about how peers' individual contextual factors, such as their sociodemographic characteristics, co-morbidity, diabetes complications, social relations, and other life events influenced how they perceived and interacted in the intervention. Further, to measure improvements in their diabetes-self management (DSM) and use of healthcare services (outcomes). Questions from the Danish National Health Survey were used to measure DSM: (eating habits, physical activity,and medication intake). Use of healthcare services was measured by the number of times (during a 12-month period) the peers' attended diabetes controls at the GP; food therapist, and ophthalmologist or had other form of contacts with relevant health care services.

All data were collected between February 2018 and April 2020.

Hypothesis: 6-month individual face-to-face peer support provided by non-professional persons with T2D can improve self-management and use of healthcare services among socially vulnerable people with T2D if contextual factors such as peers' sociodemographic characteristics, health condition, and social relations facilitate their engagement in the intervention. Potential mechanisms that generate the expected outcomes might be: peers' motivation, trust, perceived beliefs and needs; and experience of being supported by the peer supporters.

Study Overview

Detailed Description

The intervention consists of five components: Recruitment of peers and peer supporters; training of peer supporters; match making of peers and peer supporters; individual face-to-face meetings between peers and peer supporters; and ongoing supervision and network meetings for peer supporters. The peer support meetings are held approximately every second week for six months and contain three activities: 'Social and emotional support'; 'Assistance in daily management'; and 'Linkage to healthcare services'

Study Type

Interventional

Enrollment (Actual)

20

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Peers:

Inclusion Criteria:

  • Poorly regulated T2D
  • multi-morbidity
  • no employment
  • low/no education
  • no contact to the healthcare system
  • living alone with no/spare social network.

Exclusion Criteria:

- Poor regulated mental disease.

Peer supporters

Inclusion criteria:

  • Well-regulated T2D
  • Basic knowledge about T2D and the Danish healthcare system;
  • Good communication skills
  • Empathy
  • An interest in supporting a socially vulnerable person with T2D
  • Available two hours every second week for at least six-month (the intervention period).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Supportive Care
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Together on Diabetes
The intervention consists of five components: Recruitment of peers and peer supporters; training of peer supporters; matching peers and peer supporters; individual face-to-face meetings between peers and peer supporters; and ongoing supervision and network meetings for peer supporters.
Social and emotional support'; 'Assistance in daily management'; and 'Linkage to healthcare services'

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Baseline, diet habits
Time Frame: Assessed among peers before study participation, 0 month
Peers' diet habits (self-reported), Questionnaire data
Assessed among peers before study participation, 0 month
Change from Baseline, diet habits at 6 month
Time Frame: Assessed among peers after study participation, at 6 month
Improvements in the peers' diet habits (self-reported), Questionnaire data
Assessed among peers after study participation, at 6 month
Baseline, physical activity (training)
Time Frame: Assessed among peers before study participation, 0 month
Peers' physical activity level measured by time spend in a typical week on physiclal acitivty were they are breathing (eg. running, exercise gymnastics or ball sports) (self-reported), Questionnaire data
Assessed among peers before study participation, 0 month
Change from Baseline, physical activity (training) at 6 month
Time Frame: Assessed among peers after study participation, at 6 month
Improvements in the peers' physical activity level measured by time spend in a typical week on physiclal acitivty were they are breathing (eg. running, exercise gymnastics or ball sports) (self-reported), Questionnaire data
Assessed among peers after study participation, at 6 month
Baseline, physical activity (everyday activities)
Time Frame: Assessed among peers before study participation, 0 month
Peers' physical activity level measured by time spend in a typical week on everyday activities (eg. walking, cycling or gardening? (self-reported), Questionnaire data
Assessed among peers before study participation, 0 month
Change from Baseline, physical activity (everyday activities) at 6 month
Time Frame: Assessed among peers after study participation, at 6 month
Improvements in the peers' physical activity level measured by time spend in a typical week on everyday activities (eg. walking, cycling or gardening? (self-reported), Questionnaire data
Assessed among peers after study participation, at 6 month
Baseline, diabetes medication adherence
Time Frame: Assessed among peers before study participation, at 0 month
Peers' diabetes medication adherence measured by how often they forget to take their prescribed diabetes medication (self-reported), Questionnaire data
Assessed among peers before study participation, at 0 month
Baseline, diabetes medication adherence
Time Frame: Assessed among peers before study participation, at 0 month
Improvements in peers' diabetes medication adherence measured by how often they forget to take their prescribed diabetes medication (self-reported), Questionnaire data
Assessed among peers before study participation, at 0 month
Baseline, Use of healthcare services (diabetes controls at the GP)
Time Frame: ssessed among peers before study participation, 0 month
Number of diabetes controls at GP (self-reported), Questionnaire data
ssessed among peers before study participation, 0 month
Change from baseline, use of healthcare services (diabetes controls at the GP)
Time Frame: Assessed among peers after study participation, at 6 month
Improvements in the number of diabetes controls at the GP (self-reported), Questionnaire data
Assessed among peers after study participation, at 6 month
Baseline, use of healthcare services (diabetes controls at the foot therapist)
Time Frame: Assessed among peers before study participation, at 0 month
Number of diabetes controls at the food therapist) (self-reported), Questionnaire data
Assessed among peers before study participation, at 0 month
Change from baseline, use of healthcare services (diabetes controls at the foot therapist)
Time Frame: Assessed among peers after study participation, at 6 month
Improvements in the number of diabetes controls at the food therapist) (self-reported), Questionnaire data
Assessed among peers after study participation, at 6 month
Baseline, use of healthcare services (diabetes controls at the ophthalmologist )
Time Frame: Assessed among peers before study participation, at 0 month
Number of diabetes controls at the ophthalmologist ) (self-reported), Questionnaire data
Assessed among peers before study participation, at 0 month
Change from baseline, use of healthcare services (diabetes controls at the ophthalmologist )
Time Frame: Assessed among peers after study participation, at 6 month
Improvements in the number of diabetes controls at the ophthalmologist ) (self-reported), Questionnaire data
Assessed among peers after study participation, at 6 month

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 1, 2017

Primary Completion (Actual)

May 1, 2020

Study Completion (Actual)

May 1, 2020

Study Registration Dates

First Submitted

January 8, 2021

First Submitted That Met QC Criteria

January 20, 2021

First Posted (Actual)

January 25, 2021

Study Record Updates

Last Update Posted (Actual)

January 25, 2021

Last Update Submitted That Met QC Criteria

January 20, 2021

Last Verified

January 1, 2021

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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