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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04274660
Other study ID # 2S01-058 DWELL
Secondary ID 10065G00484
Status Completed
Phase N/A
First received
Last updated
Start date September 8, 2017
Est. completion date December 31, 2022

Study information

Verified date February 2023
Source Canterbury Christ Church University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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 600 patients will participate in the programme, while a non-intervention group will receive routine care for their diabetes


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.


Recruitment information / eligibility

Status Completed
Enrollment 594
Est. completion date December 31, 2022
Est. primary completion date December 31, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
DWELL (Diabetes and WELLbeing) Programme
12-week psychoeducational programme

Locations

Country Name City State
Belgium Arteveldehogeschool Ghent
France Centre Hosptalier Douai Douai
Netherlands Kinetic Analysis Breda 's-Hertogenbosch
United Kingdom Medway Community Healthcare Gillingham Kent
United Kingdom Blackthorn Trust Maidstone Kent

Sponsors (7)

Lead Sponsor Collaborator
Canterbury Christ Church University Arteveldehogeschool, Blackthorn Trust, Centre Hospitalier de Douai, Kinetic Analysis, Medway Community Healthcare, The Health and Europe Centre

Countries where clinical trial is conducted

Belgium,  France,  Netherlands,  United Kingdom, 

References & Publications (4)

Hatzidimitriadou, E., Manship, S., Thompson, T., Morris, R., Moore, J. and Hulbert, S. 2023. Evalatuation study of the diabetes and welbeing (DWELL) - Report 1: Evaluation methodology. Canterbury, UK Canterbury Christ Church University.

Hatzidimitriadou, E., Manship, S., Thompson, T., Morris, R., Moore, J. and Hulbert, S. 2023. Evaluation study of Diabetes and Wellbeing (DWELL) - Report 3: Process evaluation. Canterbury Canterbury Christ Church University.

Hatzidimitriadou, E., Manship, S., Thompson, T., Morris, R., Moore, J., Hulbert, S. and Saloniki, E.-C. 2023. Evaluation study of diabetes and wellbeing (DWELL) - Report 2: Participant outcomes. Canterbury, UK Canterbury Christ Church University.

Hatzidimitriadou, E., Manship, S., Thompson, T., Morris, R., Moore, J., Hulbert, S. and Saloniki, E.-C. 2023. Evaluation study of diabetes and wellbeing (DWELL) - Report 4: Workforce training and cost effectiveness. Canterbury. UK Canterbury Christ Church University.

Outcome

Type Measure Description Time frame Safety issue
Primary 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. Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Secondary 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) Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Secondary 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. Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Secondary 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) Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Secondary 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. Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Secondary 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) Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Secondary 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 Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Secondary 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 Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Secondary 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 Baseline, end of programme (3 months), 6 months after programme, 12 months after programme
Secondary 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. 2.5 years
Secondary 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 2.5 years
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