Healthy Eating & Active Lifestyles for Diabetes: Feasibility Trial (HEAL-D)
Primary Purpose
Type2 Diabetes
Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
HEAL-D
Control
Sponsored by

About this trial
This is an interventional treatment trial for Type2 Diabetes focused on measuring type 2 diabetes, Ethnicity, African-caribbean, Education, Self-management
Eligibility Criteria
Inclusion Criteria:
- documented diagnosis of type 2 diabetes
- self-declared African, Caribbean or Black British ethnicity
Exclusion Criteria:
- Complex dietetic needs e.g. advanced renal disease, making them unsuitable for general diet and lifestyle advice.
- Complex educational needs making them unsuitable for general group education.
- Unable to communicate in English.
Sites / Locations
- Guys and St Thomas NHS Foundation Trust
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Intervention
Control
Arm Description
HEAL-D diet and lifestyle education and behavioural change intervention, 7 sessions over 14 weeks.
Usual care.
Outcomes
Primary Outcome Measures
HbA1c
glycosylated hemoglobin, mmol/mol
Waist circumference
Waist circumference, cm
Secondary Outcome Measures
Body weight
Body weight, kg
Total cholesterol
Total cholesterol, mmol/l
LDL-cholesterol
LDL-cholesterol, mmol/l
HDL-cholesterol
HDL-cholesterol, mmol/l
triglycerides
triglycerides, mmol/l
Diabetes knowledge
Measured using the Short Diabetes Knowledge Instrument
Perceived Diabetes & Dietary Competence
Measured using the Perceived Diabetes & Dietary Competence (PDDC) questionnaire
Diabetes Empowerment
Measured using the Diabetes Empowerment Scale-Short Form (DES-SF). It measures an individuals psychosocial self-efficacy with regard to their type 2 diabetes management. It uses a 5 point scale: Strongly Disagree; Somewhat disagree; Neutral; Somewhat Agree; Strongly Agree Strongly Disagree has a score of 1 through to strongly agree with a score of 5. The questionnaire is scored by averaging scores for all completed items. Total score ranges from a minimum of 1 to a maximum score of 5. The higher the score the higher the self-efficacy/empowerment. There are no sub-scales in this measure.
Perceived social support
Measured using the Multidimensional Scale of Perceived Social Support (PSS). It measures the degree to which an individual feels socially supported. Scores are on a numerical scale from 1 to 7 with 1 being the lowest social support and 7 the highest. The scores are summed. Three subscales are reported: family; friends; and significant other. Each subscale scores a minimum 4 and maximum 28. The total score ranges from 12 to 84.Higher scores indicate higher the degree of perceived social support.
Quality of Life
The EuroQol Five Dimension Three Level (EQ-5D-3L) scale measures health status. Level 1: respondents choose one statement which best describes their health status (5 dimensions: mobility, self-care, usual activities,pain/discomfort, and anxiety/depression), coded as 1 (no problems), 2 (some problems), or 3 (extreme problems). Numerals 1-3 have no arithmetic properties and should not be used as a cardinal score.The person's health status is defined by a 5-digit number, ranging from 11111 (no problems in all dimensions) to 33333 (extreme problems in all dimensions). There are potentially 243 different scores. Level 2 is the Visual Analogue Scale giving a score from 0 to 100, higher values indicating better health. The total score ranges from 0-1, it is calculated by applying a formula that essentially attaches values ('weights') to each of the levels in each dimension. The index can be calculated by deducting the appropriate weights from 1, the value for full health (i.e. state 11111).
Diabetes-specific Quality of Life
Measured using the Problem Areas In Diabetes-5 point scale (PAID-5). Each question has five possible answers with a value from 0 to 4, with 0 representing "no problem" and 4 "a serious problem". The scores for each of the 5 questions are added up to give a total score ranging from 0 to 20, with higher scores indicating higher degree of problems with diabetes.
Dietary carbohydrate intake
Measured in grams/day from a 24 hour recall interview
Physical activity
Measured as minutes of moderate intensity exercise per day using the Motion Watch accelerometer
Full Information
NCT ID
NCT03531177
First Posted
May 3, 2018
Last Updated
March 9, 2021
Sponsor
King's College London
Collaborators
University College, London
1. Study Identification
Unique Protocol Identification Number
NCT03531177
Brief Title
Healthy Eating & Active Lifestyles for Diabetes: Feasibility Trial
Acronym
HEAL-D
Official Title
Healthy Eating & Active Lifestyle for Diabetes in UK African & Caribbean Communities: a Feasibility Trial With Process Evaluation
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
April 26, 2018 (Actual)
Primary Completion Date
May 30, 2019 (Actual)
Study Completion Date
March 30, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
King's College London
Collaborators
University College, London
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
The HEAL-D feasibility trial is a randomised control study to determine the feasibility of conducting an effectiveness trial of the Healthy Eating & Active Lifestyles for Diabetes programme; a culturally-tailored diet and lifestyle intervention for the management of type 2 diabetes in African and Caribbean communities. In this feasibility study HEAL-D will be evaluated against usual care in 80 patients with type 2 diabetes. HEAL-D is a programme of culturally-tailored diabetes self-management education and support, delivered over 7 sessions. Key outcomes are the acceptability of the programme; and recruitment and retention of the research participants. The current study will also pilot the feasibility and acceptability to participants of measuring proposed primary and secondary outcomes including HbA1c, blood lipids (triglyceride, total cholesterol, HDL-cholesterol, LDL-cholesterol), body weight, waist circumference, diabetes knowledge, diabetes and dietary competence, diabetes empowerment, perceived social support, quality of life, dietary intake, and physical activity.
Detailed Description
This study is a feasibility trial with an embedded process evaluation of the HEAL-D intervention compared with usual care. The study will use a randomised controlled trial (RCT) design, with individual patients as the unit of randomisation, evaluating the HEAL-D programme against usual care. The RCT design has been chosen primarily to evaluate the feasibility of recruiting and retaining a control arm, as well as to define what constitutes 'usual care' and the variability within that. Patients with diagnosed type 2 diabetes (T2D) will be recruited from General Practice surgeries in the London Boroughs of Lambeth and Southwark. In addition participants from the phase 1 co-design study will be invited to participate and self-referral methods will also be used, for example posters and advertisements in community locations. Patients will be eligible if they have a documented diagnosis of T2D and are of self-declared African or Caribbean ethnicity. Patients with complex therapeutic dietary needs may be ineligible if their individual needs are deemed incompatible with the aims of the intervention. Additionally patients who are unable to communicate in English will be ineligible.
A pragmatic sample size of 80 randomised patients, 40 in each arm, is anticipated to be sufficient to evaluate the programme, allowing for 20% drop-out/non-completion. As this is a feasibility trial it is not powered to detect statistically significant intervention effects, unless these estimated effects are extremely large. The purpose of the study is to assess the feasibility and acceptability of the intervention and of trial methods, and to provide estimates of key parameters such as potential effect sizes, recruitment and retention rates of the trial and participation rates of the programme, so that the optimal design of a full-scale trial can be determined.
The HEAL-D intervention consists of 7 sessions; the programme will have a flexible schedule allowing participants to attend either fortnightly or monthly sessions. Each patient who participates will be in the study for approximately 7 months and will be asked to complete two assessment visits, one at baseline and one 6-8 months later, depending on the intensity of programme attendance. A range of potential primary and secondary outcome data will be collected including HbA1c, blood lipids (triglyceride, total cholesterol, HDL-cholesterol, LDL-cholesterol), body weight, waist circumference, diabetes knowledge, diabetes and dietary competence, diabetes empowerment, perceived social support, quality of life, dietary intake, and physical activity. Participants may also participate in an interview or focus group as part of the study's process evaluation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Type2 Diabetes
Keywords
type 2 diabetes, Ethnicity, African-caribbean, Education, Self-management
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomised model, two arms. Intervention assessed against control.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
77 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Intervention
Arm Type
Experimental
Arm Description
HEAL-D diet and lifestyle education and behavioural change intervention, 7 sessions over 14 weeks.
Arm Title
Control
Arm Type
Active Comparator
Arm Description
Usual care.
Intervention Type
Behavioral
Intervention Name(s)
HEAL-D
Intervention Description
HEAL-D is a 7 session programme of self-management education and behaviour change support for African and Caribbean patients with type 2 diabetes. The sessions will support participants with behaviour change to adopt evidence-based diet and physical activity targets for type 2 diabetes. The intervention has been systematically developed with defined theory and behavioural change techniques mapped to this theory.
Intervention Type
Behavioral
Intervention Name(s)
Control
Intervention Description
Participants receive usual care from their healthcare team.
Primary Outcome Measure Information:
Title
HbA1c
Description
glycosylated hemoglobin, mmol/mol
Time Frame
6 months
Title
Waist circumference
Description
Waist circumference, cm
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Body weight
Description
Body weight, kg
Time Frame
6 months
Title
Total cholesterol
Description
Total cholesterol, mmol/l
Time Frame
6 months
Title
LDL-cholesterol
Description
LDL-cholesterol, mmol/l
Time Frame
6 months
Title
HDL-cholesterol
Description
HDL-cholesterol, mmol/l
Time Frame
6 months
Title
triglycerides
Description
triglycerides, mmol/l
Time Frame
6 months
Title
Diabetes knowledge
Description
Measured using the Short Diabetes Knowledge Instrument
Time Frame
6 months
Title
Perceived Diabetes & Dietary Competence
Description
Measured using the Perceived Diabetes & Dietary Competence (PDDC) questionnaire
Time Frame
6 months
Title
Diabetes Empowerment
Description
Measured using the Diabetes Empowerment Scale-Short Form (DES-SF). It measures an individuals psychosocial self-efficacy with regard to their type 2 diabetes management. It uses a 5 point scale: Strongly Disagree; Somewhat disagree; Neutral; Somewhat Agree; Strongly Agree Strongly Disagree has a score of 1 through to strongly agree with a score of 5. The questionnaire is scored by averaging scores for all completed items. Total score ranges from a minimum of 1 to a maximum score of 5. The higher the score the higher the self-efficacy/empowerment. There are no sub-scales in this measure.
Time Frame
6 months
Title
Perceived social support
Description
Measured using the Multidimensional Scale of Perceived Social Support (PSS). It measures the degree to which an individual feels socially supported. Scores are on a numerical scale from 1 to 7 with 1 being the lowest social support and 7 the highest. The scores are summed. Three subscales are reported: family; friends; and significant other. Each subscale scores a minimum 4 and maximum 28. The total score ranges from 12 to 84.Higher scores indicate higher the degree of perceived social support.
Time Frame
6 months
Title
Quality of Life
Description
The EuroQol Five Dimension Three Level (EQ-5D-3L) scale measures health status. Level 1: respondents choose one statement which best describes their health status (5 dimensions: mobility, self-care, usual activities,pain/discomfort, and anxiety/depression), coded as 1 (no problems), 2 (some problems), or 3 (extreme problems). Numerals 1-3 have no arithmetic properties and should not be used as a cardinal score.The person's health status is defined by a 5-digit number, ranging from 11111 (no problems in all dimensions) to 33333 (extreme problems in all dimensions). There are potentially 243 different scores. Level 2 is the Visual Analogue Scale giving a score from 0 to 100, higher values indicating better health. The total score ranges from 0-1, it is calculated by applying a formula that essentially attaches values ('weights') to each of the levels in each dimension. The index can be calculated by deducting the appropriate weights from 1, the value for full health (i.e. state 11111).
Time Frame
6 months
Title
Diabetes-specific Quality of Life
Description
Measured using the Problem Areas In Diabetes-5 point scale (PAID-5). Each question has five possible answers with a value from 0 to 4, with 0 representing "no problem" and 4 "a serious problem". The scores for each of the 5 questions are added up to give a total score ranging from 0 to 20, with higher scores indicating higher degree of problems with diabetes.
Time Frame
6 months
Title
Dietary carbohydrate intake
Description
Measured in grams/day from a 24 hour recall interview
Time Frame
6 months
Title
Physical activity
Description
Measured as minutes of moderate intensity exercise per day using the Motion Watch accelerometer
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
documented diagnosis of type 2 diabetes
self-declared African, Caribbean or Black British ethnicity
Exclusion Criteria:
Complex dietetic needs e.g. advanced renal disease, making them unsuitable for general diet and lifestyle advice.
Complex educational needs making them unsuitable for general group education.
Unable to communicate in English.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Louise M Goff, PhD
Organizational Affiliation
King's College London
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Barbara McGowan, PhD
Organizational Affiliation
Guy's and St Thomas NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Guys and St Thomas NHS Foundation Trust
City
London
ZIP/Postal Code
SE1 9RT
Country
United Kingdom
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34518159
Citation
Goff LM, Rivas C, Moore A, Beckley-Hoelscher N, Reid F, Harding S. Healthy Eating and Active Lifestyles for Diabetes (HEAL-D), a culturally tailored self-management education and support program for type 2 diabetes in black-British adults: a randomized controlled feasibility trial. BMJ Open Diabetes Res Care. 2021 Sep;9(1):e002438. doi: 10.1136/bmjdrc-2021-002438.
Results Reference
derived
PubMed Identifier
30826792
Citation
Goff LM, Moore AP, Rivas C, Harding S. Healthy Eating and Active Lifestyles for Diabetes (HEAL-D): study protocol for the design and feasibility trial, with process evaluation, of a culturally tailored diabetes self-management programme for African-Caribbean communities. BMJ Open. 2019 Mar 1;9(2):e023733. doi: 10.1136/bmjopen-2018-023733.
Results Reference
derived
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Healthy Eating & Active Lifestyles for Diabetes: Feasibility Trial
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