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Evaluation of Diabetes and WELLbeing Programme (DWELL)

Primary Purpose

Type 2 Diabetes, Type 2 Diabetes Treated With Insulin

Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
DWELL (Diabetes and WELLbeing) Programme
Sponsored by
Canterbury Christ Church University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Type 2 Diabetes

Eligibility Criteria

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

Inclusion Criteria:

  • Clinical diagnosis of type 2 diabetes
  • Over the age of 18

Exclusion Criteria:

  • Under the age of 18
  • Pregnant women
  • Individuals who do not have the mental capacity to participate

Sites / Locations

  • ArteveldehogeschoolRecruiting
  • Centre Hosptalier DouaiRecruiting
  • Kinetic AnalysisRecruiting
  • Medway Community HealthcareRecruiting
  • Blackthorn TrustRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

DWELL Intervention

DWELL non-intervention/Control

Arm Description

People with type 2 diabetes participating in the 12-week DWELL (Diabetes and WELLbeing) Programme

People with type 2 diabetes who are receiving routine care from their GP and healthcare team. People with type 2 diabetes will continue to receive routine standard care. Routine care in this respect constitutes usual health and social care or any other nationally or locally commissioned education programmes

Outcomes

Primary Outcome Measures

Change in diabetes self-management as assessed by the Diabetes Self-Care Activities Measure
Changes in self-management and self-care will be measured using the Diabetes Self-Care Activities Measure at four time points. The SDSCA assesses aspects of the diabetes regimen. Higher scores indicate greater taking of prescribed medication and undertaking footcare regime.

Secondary Outcome Measures

Change in quality of life as assessed by the Short Form Health Survey (SF-12)
Changes in health related quality of life will be measured using the Short Form Health Survey (SF-12) at four time points. SF-12 measures eight health domains to assess physical health (min 6, max 20 - higher scores indicate better physical health) and mental health (min 6, max 24 - higher scores indicate better mental health)
Change in levels of physical activity as assessed by the International Physical Activity Questionnaire (IPAQ)
Changes in levels of physical activity will be measured using the International Physical Activity Questionnaire (IPAQ) at four time points. IPAQ collects information on physical activity participation in three domains as well as sedentary behaviour. There is no min or max score - participants indicate how much exercise they do per week which is converted into MET minutes. Greater MET minutes indicate greater levels of physical activity.
Change in illness perception as assessed by the Illness Perception Questionnaire (IPQ-R)
Changes in perception and attitudes towards type 2 diabetes will be measured using the Illness Perception Questionnaire (IPQ-R) at four time points. IPQ-R measures an individual's beliefs and feelings about their illness. The IPQ-R is split into 7 sub-scales: Timeline (min 6, max 30 - higher scores indicate participants expect diabetes to last longer); Consequences (min 6, max 30 - higher scores indicate perceived worse consequences of diabetes); Personal Control (min 6, max 30 - higher scores indicate higher perceived control over diabetes); Treatment Control (min 5, max 25 - higher scores indicate higher perceived effect of treatment); Illness Coherence (min 5, max 25 - higher scores indicate better perceived understanding of illness); Timeline Cyclical (min 4, max 20 - higher scores indicate greater unpredictability of diabetes symptoms); Emotional Representations (min 6, max 30 - higher scores indicate more negative emotions associated with diabetes)
Change in psychosocial self-efficacy as assessed by the Diabetes Empowerment Scale (DES-SF)
Changes in self-efficacy will be measured using the Diabetes Empowerment Scale (DES-SF) at four time points. DES-SF measures changes in psychosocial self-efficacy. Minimum score is 8, max is 40. Higher scores indicate greater sense of empowerment to self-manage condition.
Change in eating behaviour as assessed by the Dutch Eating Behaviour Questionnaire (DEBQ)
Changes in eating behaviour will be measured using the Dutch Eating Behaviour Questionnaire (DEBQ) at four time points. DEBQ assesses three distinct eating behaviours in adults: Emotional Eating (min 10, max 50 - higher scores indicate the patient makes more effort to restrain eating) ; External Eating (min 13, max 65 - higher scores indicate patient eats more for emotional reasons); Restrained Eating (min 10, max 50 - higher scores indicate more motivated to eat by external factors, such as the smell and look of food)
Change in Body Mass Index (BMI) as assessed by height and weight
Changes in height and weight will be combined to report BMI in kg/m^2 where a lower score indicates an improvement for this outcome
Change in waist circumference
Changes in waist circumference will be measured and reported in cm where a lower measurement indicates an improvement for this outcome
Change in average blood glucose levels as assessed by Hemoglobin A1c levels (HbA1c)
Changes in blood glucose (sugar) levels will be assessed by reports of HbA1c blood test results, where a lower score indicates improvement in this outcome
Quality Adjusted Life Years (QALYs)
Health related quality of life will be measured using the EuroQol Five Dimensions (EQ-5D-5L). The EQ-5D contains 5 sub-scales with a min score of 1 and max score of 3. Higher scores indicate worse mobility, worse ability to self-care, worse ability to perform usual activities, more pain and more anxiety. Utility values will also be multiplied by the time spent in each state to generate QALYs. 1 QALY is equivalent to perfect health while less than perfect health carries a QALY between 0 and 1. The higher the number of QALYs gained the better the health outcomes for people living with type 2 diabetes.
Cost effectiveness
The cost of Quality Adjusted Life Years (QALYs) of people with type 2 diabetes in the intervention group will be compared with the control group to illustrate cost effectiveness of the DWELL Programme

Full Information

First Posted
February 5, 2020
Last Updated
July 27, 2021
Sponsor
Canterbury Christ Church University
Collaborators
Interreg 2 Seas Mers Zeeen, Medway Community Healthcare, Blackthorn Trust, Arteveldehogeschool, Kinetic Analysis, Centre Hospitalier de Douai
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1. Study Identification

Unique Protocol Identification Number
NCT04274660
Brief Title
Evaluation of Diabetes and WELLbeing Programme
Acronym
DWELL
Official Title
Evaluation of the Diabetes and WELLbeing (DWELL) Programme for People With Type 2 Diabetes
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
September 8, 2017 (Actual)
Primary Completion Date
March 31, 2023 (Anticipated)
Study Completion Date
March 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Canterbury Christ Church University
Collaborators
Interreg 2 Seas Mers Zeeen, Medway Community Healthcare, Blackthorn Trust, Arteveldehogeschool, Kinetic Analysis, Centre Hospitalier de Douai

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
This study evaluates the impact of 'DWELL' - a 12-week psycho-social education programme designed to help people with type 2 diabetes to better self-manage their condition. Up to 800 patients will participate in the programme, while a non-intervention group will receive routine care for their diabetes
Detailed Description
The DWELL (Diabetes and WELLbeing) 12-week programme has been designed to incorporate specific elements of diabetes education and is underpinned by motivational interviewing to ensure it is tailored to individuals. Each of the four elements of the programme - education, nutrition, physical activity and wellbeing - have been carefully selected based on previous research into diabetes education. The Canterbury Christ Church University (CCCU) DWELL Team are responsible for the evaluation of DWELL, which will explore whether the combination of the programme elements is effective in improving self-management. Additionally, a process evaluation and cost effectiveness analysis will be conducted alongside participant outcomes The programme will be delivered at five sites (two in the UK, one in Belgium, one in France, one in the Netherlands). The CCCU DWELL research team will be responsible for quality assurance, management and analysis of data, sample size assessment and reporting of adverse events. Each delivery site is responsible for adhering to their own Standard Operating Procedures.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type 2 Diabetes, Type 2 Diabetes Treated With Insulin

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Model Description
Participants will be invited to take part in the 12-week DWELL Programme (the intervention) based on their eligibility as per the inclusion criteria. They will all receive the psycho-social education element in addition to two motivational interviews. Each element will be evaluated alone and in combination. The non-intervention group will be recruited in one of two ways - they will either be people with type 2 diabetes who do not wish to participate in the 12-week programme, or they are receiving routine care (which, for UK participants, is a locally commissioned 6-week programme).
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
800 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
DWELL Intervention
Arm Type
Experimental
Arm Description
People with type 2 diabetes participating in the 12-week DWELL (Diabetes and WELLbeing) Programme
Arm Title
DWELL non-intervention/Control
Arm Type
No Intervention
Arm Description
People with type 2 diabetes who are receiving routine care from their GP and healthcare team. People with type 2 diabetes will continue to receive routine standard care. Routine care in this respect constitutes usual health and social care or any other nationally or locally commissioned education programmes
Intervention Type
Behavioral
Intervention Name(s)
DWELL (Diabetes and WELLbeing) Programme
Intervention Description
12-week psychoeducational programme
Primary Outcome Measure Information:
Title
Change in diabetes self-management as assessed by the Diabetes Self-Care Activities Measure
Description
Changes in self-management and self-care will be measured using the Diabetes Self-Care Activities Measure at four time points. The SDSCA assesses aspects of the diabetes regimen. Higher scores indicate greater taking of prescribed medication and undertaking footcare regime.
Time Frame
Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Secondary Outcome Measure Information:
Title
Change in quality of life as assessed by the Short Form Health Survey (SF-12)
Description
Changes in health related quality of life will be measured using the Short Form Health Survey (SF-12) at four time points. SF-12 measures eight health domains to assess physical health (min 6, max 20 - higher scores indicate better physical health) and mental health (min 6, max 24 - higher scores indicate better mental health)
Time Frame
Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Title
Change in levels of physical activity as assessed by the International Physical Activity Questionnaire (IPAQ)
Description
Changes in levels of physical activity will be measured using the International Physical Activity Questionnaire (IPAQ) at four time points. IPAQ collects information on physical activity participation in three domains as well as sedentary behaviour. There is no min or max score - participants indicate how much exercise they do per week which is converted into MET minutes. Greater MET minutes indicate greater levels of physical activity.
Time Frame
Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Title
Change in illness perception as assessed by the Illness Perception Questionnaire (IPQ-R)
Description
Changes in perception and attitudes towards type 2 diabetes will be measured using the Illness Perception Questionnaire (IPQ-R) at four time points. IPQ-R measures an individual's beliefs and feelings about their illness. The IPQ-R is split into 7 sub-scales: Timeline (min 6, max 30 - higher scores indicate participants expect diabetes to last longer); Consequences (min 6, max 30 - higher scores indicate perceived worse consequences of diabetes); Personal Control (min 6, max 30 - higher scores indicate higher perceived control over diabetes); Treatment Control (min 5, max 25 - higher scores indicate higher perceived effect of treatment); Illness Coherence (min 5, max 25 - higher scores indicate better perceived understanding of illness); Timeline Cyclical (min 4, max 20 - higher scores indicate greater unpredictability of diabetes symptoms); Emotional Representations (min 6, max 30 - higher scores indicate more negative emotions associated with diabetes)
Time Frame
Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Title
Change in psychosocial self-efficacy as assessed by the Diabetes Empowerment Scale (DES-SF)
Description
Changes in self-efficacy will be measured using the Diabetes Empowerment Scale (DES-SF) at four time points. DES-SF measures changes in psychosocial self-efficacy. Minimum score is 8, max is 40. Higher scores indicate greater sense of empowerment to self-manage condition.
Time Frame
Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Title
Change in eating behaviour as assessed by the Dutch Eating Behaviour Questionnaire (DEBQ)
Description
Changes in eating behaviour will be measured using the Dutch Eating Behaviour Questionnaire (DEBQ) at four time points. DEBQ assesses three distinct eating behaviours in adults: Emotional Eating (min 10, max 50 - higher scores indicate the patient makes more effort to restrain eating) ; External Eating (min 13, max 65 - higher scores indicate patient eats more for emotional reasons); Restrained Eating (min 10, max 50 - higher scores indicate more motivated to eat by external factors, such as the smell and look of food)
Time Frame
Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Title
Change in Body Mass Index (BMI) as assessed by height and weight
Description
Changes in height and weight will be combined to report BMI in kg/m^2 where a lower score indicates an improvement for this outcome
Time Frame
Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Title
Change in waist circumference
Description
Changes in waist circumference will be measured and reported in cm where a lower measurement indicates an improvement for this outcome
Time Frame
Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Title
Change in average blood glucose levels as assessed by Hemoglobin A1c levels (HbA1c)
Description
Changes in blood glucose (sugar) levels will be assessed by reports of HbA1c blood test results, where a lower score indicates improvement in this outcome
Time Frame
Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Title
Quality Adjusted Life Years (QALYs)
Description
Health related quality of life will be measured using the EuroQol Five Dimensions (EQ-5D-5L). The EQ-5D contains 5 sub-scales with a min score of 1 and max score of 3. Higher scores indicate worse mobility, worse ability to self-care, worse ability to perform usual activities, more pain and more anxiety. Utility values will also be multiplied by the time spent in each state to generate QALYs. 1 QALY is equivalent to perfect health while less than perfect health carries a QALY between 0 and 1. The higher the number of QALYs gained the better the health outcomes for people living with type 2 diabetes.
Time Frame
2.5 years
Title
Cost effectiveness
Description
The cost of Quality Adjusted Life Years (QALYs) of people with type 2 diabetes in the intervention group will be compared with the control group to illustrate cost effectiveness of the DWELL Programme
Time Frame
2.5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of type 2 diabetes Over the age of 18 Exclusion Criteria: Under the age of 18 Pregnant women Individuals who do not have the mental capacity to participate
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sharon Manship, MSc, MA
Phone
01634 894472
Email
sharon.manship@canterbury.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Eleni Hatzidimitriadou, PhD
Organizational Affiliation
Canterbury Christ Church University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Arteveldehogeschool
City
Ghent
ZIP/Postal Code
9000
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ruben Vanbosseghem
Phone
+32 9 234 90 00
Email
ruben.vanbosseghem@arteveldehs.be
Facility Name
Centre Hosptalier Douai
City
Douai
ZIP/Postal Code
59507
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marie Duezcalzada
Phone
+33 3 27 94 70 00
Email
Marie.Duezcalzada@ch-douai.fr
Facility Name
Kinetic Analysis
City
Breda
State/Province
's-Hertogenbosch
ZIP/Postal Code
5211 DA
Country
Netherlands
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maarten Gijssel
Phone
+31 6 21566017
Email
mpe.gijssel@kinetic-analysis.com
Facility Name
Medway Community Healthcare
City
Gillingham
State/Province
Kent
ZIP/Postal Code
ME8 0PZ
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Julie Webster
Phone
01634 334620
Email
julie.webster1@nhs.net
Facility Name
Blackthorn Trust
City
Maidstone
State/Province
Kent
ZIP/Postal Code
ME16 9AN
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nathalie Belmas
Phone
01622 828382
Email
nathalie@blackthorn.org.uk

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
Anonymous participant data relating to results in publications with regards to primary and secondary outcome measures will be shared through publishing platforms. Anonymised individual participant datasets may be shared via a suitable public data repository. A final report of the evaluation study will be made available via the Canterbury Christ Church University DWELL Project web page.
IPD Sharing Time Frame
It is anticipated that the study protocol will be published in a suitable academic journal by 31 December 2020. Individual participant data sets relating to the study will be made available via an appropriate data repository starting 6 months after formal publication of results. The final report of the evaluation study will be available on Canterbury Christ Church University DWELL Project web page by 31 December 2020.
IPD Sharing Access Criteria
Anonymised participant data sets relating to publications will be shared through the control measures of the publishing journals, such as full access to subscribers.

Learn more about this trial

Evaluation of Diabetes and WELLbeing Programme

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