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Feasibility, acceptability and outcomes at a 12-month follow-up of a novel community-based intervention to prevent type 2 diabetes in adults at high risk: mixed methods pilot study
  1. Linda Penn1,2,
  2. Vicky Ryan1,
  3. Martin White1,2
  1. 1Institute of Health and Society, Newcastle University, Newcastle upon Tyne, UK
  2. 2Fuse, UKCRC Centre for Translational Research in Public Health
  1. Correspondence to Linda Penn; linda.penn{at}


Objectives and design Lifestyle interventions can prevent type 2 diabetes (T2D) in adults with impaired glucose tolerance. In a mixed methods pilot study, we aimed to assess the feasibility, acceptability and outcomes at a 12-month follow-up of a behavioural intervention for adults at risk of T2D.

Participants Adults aged 45–65 years with a Finnish Diabetes Risk Score (FINDRISC) ≥11.

Setting The intervention was delivered in leisure and community settings in a local authority that ranks in the 10 most socioeconomically deprived in England.

Intervention A 10-week supported programme to promote increased physical activity (PA), healthy eating and weight loss was delivered by fitness trainers as twice-weekly group PA or cookery sessions, each followed by behavioural counselling with support to 12 months.

Outcome measures We assessed feasibility and acceptability of the intervention, and change in behavioural and health-related outcomes at 6 and 12 months.

Results From 367 registers of interest, 218 participants were recruited to the programme with baseline mean (SD): age 53.6 (6) years, FINDRISC 13.9 (3.1), body mass index 33.5 (5.9) kg/m2, waist circumference 108.1 (13.7) cm, PA levels (self-report): daily total 49.1 (5.9) metabolic-equivalent (MET) h/day. Follow-up at 12 months was completed by 134 (61%) participants, with an estimated mean (95% CI) change from baseline in weight −5.7 (−7.8 to −2.8); −2.8 (−3.8 to −1.9) kg, waist circumference −7.2 (−9.2 to −5.2); −6.0 (−7.1 to −5.0) cm, and PA level 7.9 (5.8 to 10.1); 6.7 (5.2 to 8.2) MET h/day equivalent, for men and women, respectively (from covariance pattern mixed models). Participants reported an enjoyable, sociable and supportive intervention experience.

Conclusions Participants’ views indicated a high level of intervention acceptability. High retention and positive outcomes at 12 months provide encouraging indications of the feasibility and potential effectiveness of the intervention. A definitive trial of this intervention is warranted.

  • Diabetes & Endocrinology
  • Public Health
  • Preventive Medicine

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Strengths and limitations of this study

  • Social marketing and modelling strategies were used to design an engaging intervention.

  • The recruitment campaign was successful in reaching the target population, but was time consuming.

  • Positioning the intervention in leisure services helped to avoid ‘medicalising’ type 2 diabetes risk and facilitated the provision of a variety of physical activities with opportunities for maintenance of these postprogramme. This mode of delivery is scalable, but assessment of cost-effectiveness is necessary.

  • The group-based physical activity and cookery sessions encouraged social support, engagement and positive reinforcement regarding behaviour change.

  • More women than men were recruited, although retention in the programme was slightly greater for men than women.

  • We identified a need to adapt the programme to attract people from ethnic minority communities.


Type 2 diabetes (T2D) is an increasingly prevalent chronic disease that is progressive, debilitating and costly to treat.1 There is strong evidence from efficacy trials that onset of T2D can be delayed or prevented by lifestyle interventions in adults with impaired glucose tolerance (IGT),2 ,3 but translating such interventions to effective, routine delivery remains challenging. Early translational diabetes prevention studies conducted in Finland, Germany and the US assessed weight loss as an intermediate health outcome, thus assuming that weight loss, achieved through these interventions delivered to high-risk individuals, would predict reduced T2D incidence.4 More recently, a translational trial delivered to adults at high risk in a primary care setting, with a 4.2-year median follow-up and T2D incidence as the primary outcome, demonstrated 36.5% relative risk reduction (p < 0.005) in T2D incidence in the lifestyle intervention group compared to a usual care control group.5 This risk reduction is less than the 57% risk reduction achieved in some efficacy trials.6 The authors of this primary care trial acknowledge the difficulties in translating evidence for effective implementation and suggest that “the feasibility and effectiveness of lifestyle interventions need to be validated within the population in which they are intended to be used.”5

The UK National Institute for Health and Care Excellence (NICE) guidance for preventing T2D in high-risk individuals identified evidence gaps relating to risk identification of those suitable for lifestyle-change programmes and the need for translation of research evidence to UK practice.3 A report commissioned by NICE highlighted the increased prevalence of T2D in low socioeconomic status groups and acknowledged that engaging people from these groups in preventive interventions is challenging.7

Translational T2D prevention studies have generally used classroom-based behavioural counselling4 ,8 and this approach is advocated in the development and implementation of a European Guideline and Training Standard for Diabetes Prevention (IMAGE) guidelines.9 ,10 Similarly, the Good Ageing in Lahti region (GOAL) before-and-after implementation study for T2D prevention used a structured counselling programme that drew on social cognitive and self-regulation theories of behaviour change.11 However, the Finnish Diabetes Prevention Study (DPS)12 and American Diabetes Prevention Programme (DPP)13 trials (which provided efficacy evidence for T2D prevention) both included group delivered physical activity (PA) sessions. Experiential learning theory emphasises the central role that a ‘here-and-now’ concrete experience, along with observation and reflection, plays in promoting subsequent higher order purposeful action.14 In this experiential approach, performing an action in a specific instance and considering its effects is precedent to generalisation.15 We therefore developed an alternative approach to intervention delivery that included group delivered PA sessions to provide immediate experience of different exercise activities, facilitate peer interaction and accommodate different learning styles.16 We have drawn on experiential learning theory as well as behaviour change theories and techniques in intervention development.17–19

We report on the feasibility, acceptability and behavioural and health-related outcomes at a 12 month follow-up of a novel community-based intervention called ‘New life, New you’ (NLNY), directed at adults at risk of T2D. NLNY was novel in its delivery via supported group PA and cookery sessions, each followed by reflection, advice and counselling.20 ,21

In England, health improvement responsibilities are assigned to local government (from April 2013). Thus, NLNY, which was designed as a health and leisure service partnership to be delivered by local authority employed fitness trainers, offers a model with strong potential for future public health commissioning and service delivery. Feasibility and acceptability of this novel intervention were assessed in preparation for a definitive effectiveness trial.



We aimed to assess the feasibility, acceptability and likely effectiveness of the intervention to change PA, weight and other health-related outcomes at 12 months of follow-up.

Study design, participants and data collection

We used mixed methods to assess process and outcomes at 6 and 12 months of follow-up,22 using an uncontrolled before-and-after study design, with embedded qualitative interviews.

Two participant cohorts were recruited between March 2009 and November 2010, the first supported by social marketing campaigns and the second by word of mouth or ‘signposted’ from primary care. Inclusion criteria were: age 45–65 years, living in central Middlesbrough UK, and with elevated risk of T2D. Individualised 10 year risk of T2D was determined at baseline using the Finnish Diabetes Risk Score (FINDRISC), a prospective risk assessment tool that uses simple, non-invasive measures, including height, weight and waist circumference, as well as questions about family history and lifestyle.23 To give an indication of socioeconomic status, we used home post codes to assign the English Index of Multiple Deprivation (IMD), an ecological, composite measure based on routinely available data in seven categories of deprivation (income, employment, health and disability, education skills and training, barriers to housing and other services, crime and living environment) at the Lower Super Output Area (LSOA: a small administrative area with a population of about 1500) level to each participant.24 Previous diagnoses of T2D or inability to participate in moderate PA were exclusion criteria. Details of the target population, and recruitment strategies have been reported previously.20 ,21 Participants completed the standard local authority leisure services questionnaire, which included questions regarding medication, diagnosed medical conditions and any other condition that might prevent people from participating in PA. The leisure services standard protocol for reporting injury or other adverse side effects was used. Following a brief screening (self-report of: age, area of domicile and history of T2D), potential participants were invited to attend an individual assessment that was conducted by one of the NLNY health and fitness trainers in a convenient community location. The consultation incorporated motivational interviewing techniques to promote engagement in the intervention.25 After their baseline assessment, those with FINDRISC 11–20 who wished to participate were allocated to the intervention programme. Those with FINDRISC>20 were advised to see their general practitioner (GP) and were able to join the programme with their GP's permission (providing there was no diagnosis of T2D). The trainers conducted further assessments at 6 and 12 months in one-to-one consultations.

To assess intervention feasibility and acceptability, we recorded recruitment and retention through the programme and follow-up. We conducted qualitative interviews with participants at 6 and 12 months of postprogramme. The interview topic guide was developed from our previous research in this area.26 Interviewees were purposively selected for success in PA increase at 6 or 12 months of follow-up. Interviews were recorded and transcribed verbatim. As part of the qualitative evaluation, we sought to elicit participants’ views on acceptability of the intervention and research procedures. Participant perspectives of their behaviour changes are reported separately.21

Outcome measurements

To evaluate likely effectiveness, the primary outcome measures were change in PA levels and variety. These were assessed through a self-report instrument that we developed from the PA diary used in the Newcastle arm of the European Diabetes Prevention Study (EDIPS-Newcastle) randomised controlled trial.27 We calculated the daily total PA level in metabolic-equivalent tasks for each hour (MET h) from a 24 h recall, recorded in half-hour periods of activity level (eg, lying down=1, standing=3, brisk walking=5, strenuous activities=8).28 The amount and variety of leisure time PA over level 5 was recorded as a recall of type of activity and number of sessions of each activity of at least 15 min duration over the previous week. Secondary outcomes were change in weight and waist measurements and FINDRISC.23 Dietary assessment was based on questions about specific foods (number of portions of fruit and vegetables consumed daily, and type of bread, milk and fat usually consumed), and was aligned with the dietary advice given to participants. All measures were assessed at each time point.

Intervention development

Intervention design built on research evidence for T2D prevention including the Finnish DPS12 and EDIPS-Newcastle.26 ,27 The intervention was developed in accordance with the UK National Social Marketing Centre benchmark criteria,29 designed for adults living in socioeconomically disadvantaged areas, and intended to be delivered in leisure and community settings.20 ,21 Market segmentation identified target groups as middle-aged and older men and women on low incomes.30 Consultations with stakeholders (potential participants and experienced local fitness trainers) informed creative work with the delivery staff to develop the intervention design, name, logo and project documents, all of which were refined in usability testing.31


NLNY trainers delivered a 10-week programme of twice-weekly 1.5 h sessions to groups of 15–20 participants. Participant preferences, for example for a single-sex activity group or for particular PAs, were accommodated where possible. Each NLNY session comprised a supervised PA or, on two or three occasions within each 10-week programme, a cookery session, followed by a reflective discussion that covered PA, nutrition, weight management and strategies for behaviour change. Monthly NLNY newsletters with information, advice and recipes were available to participants, mostly online. PAs centred on the interests of each participant group, with flexibility to repeat popular activities. Sessions were leisure centre based, but also included trainer-led walks. The supported cookery sessions were designed to encourage healthy eating and to demonstrate the ease with which healthy food could be prepared. Nutritional information incorporated the importance of reading food labels with advice based on the Eat-well plate,32 including reduction in fat and increase in fibre intake, in line with the DPS protocol and NICE guidance.3 ,12 Weight reduction was advised for those overweight, who were the majority. The trainers introduced behaviour change strategies (including goal setting, action planning, barrier identification, social support, self-monitoring, advance planning for relapse prevention and contingent rewards), as the need arose, with regular repetition during the supported sessions.18

At the end of the 10-week programme, participants who had completed ≥80% attendance received an ‘access to leisure’ card that enabled free leisure service use for 12 months. After the programme, ongoing support with regular mobile phone text message and email reminders, ‘drop-in’ activity sessions and encouragement to join in local events such as organised walks and runs continued up to the assessment at 12 months of follow-up. The full intervention manual is available from the corresponding author.

Data analysis

We analysed outcome data using SPSS (IBM SPSS Inc, V.17) and SAS/STAT, V.9.2 software.33 For this feasibility study, analyses of the data collected were mainly descriptive. For repeated measures analysis of continuous outcome variables, we used covariance pattern mixed models which allow appropriate estimation of the mean change (and associated SE) between visits, allowing for missing observations over time.34 We estimated (with 95% CIs) mean change from baseline to 6 and 12 months for PA level, weight, waist circumference and FINDRISC data for those participants who started the 10-week programme. From the available self-report data, we report the number and percentage of those who participated in different activities in the previous week and the number and percentage of different foods consumed within food groups at each time point for those who completed 12 months in the study.

We analysed transcribed data, from the interview study, using the framework approach.35 A priori themes explicit in the topic guide were extended with themes emerging from the data. NVivo software was used to arrange the data. Detailed qualitative analysis, based on the theoretical domains framework, is reported separately.19 ,36 For the analysis reported here, key themes relating to acceptability were extracted along with illustrative quotes.


From 271 registers of interest for the first cohort 166 (61%), participants were recruited to the programme, including 56 (26%) recruited via word of mouth. From 96 registers of interest for the second cohort, 52 (54%) participants were recruited, including 44 (85%) recruited via word of mouth. In total, there were 367 registers of interest and the trainers recruited 218 (59%) participants to the programme. Just over half (53%) of the NLNY participants lived in an LSOA within the lowest quintile of deprivation based on 2010 IMD ranks for all England. A total of 134 (61%) programme group participants completed follow-up at 12 months. More women than men were recruited, although this difference was less in the second cohort, and a slightly higher proportion of men than women completed the 12-month follow-up. A flow chart of progress through the NLNY programme to 12 months of follow-up is detailed in figure 1.

Figure 1

Flow chart of recruitment and progress through the ‘New life, New You’ pilot evaluation.

Baseline data (continuous variables) for all those recruited to the programme and for male and female participants separately are shown in table 1 and distributions across key categories of these variables are shown in table 2. A total of 194 (89%) participants were recorded as overweight or obese, of which 64 (29%) were severely obese (body mass index, BMI>35 kg/m2). Of the men recruited, 61 (91%) recorded a waist circumference >91 cm; 126 (83%) of women recorded a waist circumference >83 cm. Participants reported taking part in PA at a level of >5 MET h/day for only 1 h/day on average with one activity being the median number of PA types. The trainers recruited 21 participants with baseline FINDRISC<11, all of whom were overweight and inactive, into the programme. The question, “Do you smoke currently?” was answered by 125 (57%) participants, of whom 3 men and 3 women reported currently smoking. The question, “Have you ever smoked?” was answered by 140 (64%) participants, of whom 20 men and 44 women reported smoking at some time previously.

Table 1

Mean (SD) for continuous baseline variables of ‘New life, New You’ participants, n=218 (men=67, women=151)

Table 2

Numbers (%) in each category of baseline variable for ‘New life, New You’ participants

Baseline values for key variables were mostly similar for those who completed 12 months of follow-up and for those who left the study early. However, participants who dropped out of the programme by 10 weeks or left before 6 or 12 months of follow-up came from significantly more deprived areas than those who completed these follow-up assessments, as shown in table 3.

Table 3

Mean (SD) for key baseline variables by retention/attrition at each follow-up stage

Changes in key variables are shown in table 4. The results suggest overall increases in PA levels (total and leisure time), an increase in the variety of PA and decreases in the BMI, weight, waist circumference and FINDRISC. Changes were greater in the first 6 months of follow-up than in the period from 7 to 12 months. Nevertheless, beneficial changes in all outcomes occurred between 0 and 12 months with estimated mean (95% CI) change from baseline in weight −5.7 (−7.8 to −2.8); −2.8 (−3.8 to −1.9) kg, waist circumference −7.2 (−9.2 to −5.2); −6.0 (−7.1 to −5.0) cm and PA level 7.9 (5.8 to 10.1); 6.7 (5.2 to 8.2) MET h/day equivalent for men and women, respectively.

Table 4

Model estimates with 95% CIs for key variables at baseline with changes at 6 and 12 months of follow-up for men and women separately

Table 5 shows the change in numbers (%) participating in specific leisure time activities at baseline, 6 and 12 months. Participation in gym-based activities, sports and ‘other’ activities (ie, any activities not otherwise specified, including the popular aqua-fit sessions) showed substantial increases over time.

Table 5

Number (%) of participants engaging in each leisure time physical activity (with level greater than 5 MET h equivalent) in the previous week*

Table 6 shows changes in numbers (%) consuming categories of specific foods at baseline, 6 and 12 months. There were notable increases in consumption of brown bread, soft margarine and five or more portions of fruit and vegetables/day, and decreases in consumption of white bread, butter and hard margarine.

Table 6

Number (%) of participants eating specific categories of food at baseline, 6 and 12 months of follow-up*

Table 7 shows key themes and associated quotations relating to acceptability of the intervention, derived from the qualitative interviews. The intervention delivery environment was viewed as welcoming, friendly, sociable, enjoyable, comfortable and convenient. The only negative comment was about the potential for disruptive elements within groups, although this comment was balanced by an appreciation of the trainers’ efforts to contain this. Participants had high praise for the trainers and would recommend the programme to others.

Table 7

Acceptability of the New Life New You intervention: key themes from participant interviews and illustrative quotes


Statement of principal findings

Most participants came from areas of social deprivation, reflecting the target population, and fewer men than women were recruited. High retention and further recruitment by word-of-mouth recommendation, along with positive comments in the qualitative interviews, suggest high levels of acceptability of the intervention. Positive outcomes at 12 months, including increased PA, weight loss, reduction in waist circumference and FINDRISC, and increase in the consumption of fruit and vegetables, are encouraging indications of the likely effectiveness of the intervention. Intervention delivery, by fitness trainers in leisure and community settings incorporating robust outcome data collection for monitoring purposes, provides a viable model for service provision in the UK.

Almost all NLNY participants were overweight or obese at baseline, with elevated risk of developing T2D. Just over half (53%) of the participants were living in areas located in the lowest, and 65% in the lowest two, quintiles of deprivation based on 2010 IMD ranks for all England. Recruitment and retention of people from this population in a preventive intervention is challenging and the retention rate of 61% at 12 months, with many participants recruited by word of mouth, demonstrates intervention acceptability. Mean beneficial change was demonstrated in measures of PA and in objective measures of weight and waist circumference, resulting in reduction in FINDRISC for many participants. The main areas of PA increase were gym-based and sports activities (including badminton) as well as popular ‘aqua-fit’ sessions (which were provided separately for men and women). Walking, hobbies and swimming activities were fairly consistent across the study time period, which suggests that the new activities were additions rather than replacements.

The dietary assessment was limited by resources and a perceived need to minimise respondent burden. Of interest was the increase in reported portions of fruit and vegetables consumed per day. There were only modest beneficial changes in other food groups. Refinement of dietary advice to promote wholemeal (rather than brown) bread and skimmed (rather than semiskimmed) milk should be considered.

Strengths and limitations of the study

Recruitment and retention

Intervention development was strengthened by drawing on social marketing (profiling a target population, pretesting intervention design through stakeholder consultations and positioning in community settings) and modelling (using behavioural and intermediate health outcomes) strategies to ensure an appropriate, engaging and pragmatic intervention.31 ,37 The promotional campaign, led by the fitness trainers, was time consuming and ‘signposting’ from the National Health Services (NHS) Health Checks programme within primary care might be a more efficient long-term option for recruitment.38 However, we cannot be sure whether this different recruitment strategy would affect retention and outcomes.

More women than men were recruited, in common with previous diabetes prevention studies,12 ,13 and this remains a concern, especially in view of the greater prevalence of T2D in men.39 Our social marketing approach to intervention development led us to provide single-sex PA classes. However, further gender-sensitive strategies need to be developed to attract men to participate in T2D prevention interventions.40

Themes from the interview study suggest a high degree of acceptability. However, these interviews were conducted with participants who remained in the study and may not reflect the perspectives of those who dropped out. Those who left the study early tended not to respond to contacts. Participants were recruited from the community and although the early recruitment strategy involved advertising the programme, later participants were mainly recruited through word of mouth. We suggest that as later recruits only became interested in this opportunity through those already participating, they were not a population subfraction with prior interest in supervised PA training.

We did not exclude ethnic minorities from taking part in the programme, but as only two people from these groups became involved we identified this as a design limitation, considering the potentially raised prevalence of T2D within the UK South Asian and African communities.3 We are currently developing an adaptation of the programme,41 specifically to target local ethnic minority communities, which also includes provision for younger age participants from these groups in line with NICE guidance.3 This adaptation will be similarly assessed for feasibility, acceptability and outcomes at 12 months.

Recruitment to this study relied on a self-reported FINDRISC.23 We agreed on some flexibility for inclusion in this feasibility study because the FINDRISC algorithm includes a heavily weighted family history question and validity is compromised where data on family history are unavailable. Family history in risk score assessment introduces bias (eg, for people from single-parent families or people with younger than average parents),42 which might have importance for this socioeconomically disadvantaged participant population. Seven of those recruited to NLNY who did not report family history at baseline did so at 6 months, and we know that some of this difference was due to new T2D diagnoses in family members. The participants with baseline FINDRISC<11 were all overweight and inactive.23 However, this flexibility in recruitment introduces a design limitation and highlights the difficulty that the trainers experienced in ‘turning away’ people who were keen to participate in the programme. This difficulty was an important finding from the feasibility evaluation and an alternative strategy will be needed for a definitive trial. A risk score and confirmatory blood test, as advised in NICE guidance, would ensure more precise inclusion criteria. In this context, point of care glycated haemoglobin (HbA1c) may be convenient. HbA1C cut-points to identify high-risk individuals are recommended in NICE guidance, but these do not identify a population with IGT and the appropriate HbA1c cut-points for the purpose of preventive interventions are untested.3

Data administration

In this pilot study, we asked the fitness trainers to undertake risk assessment and collect all data. This strategy was designed to reflect the likely future practice, with inbuilt potential for robust monitoring and quality assurance measures for service provision. However, data collection involved new procedures for the fitness trainers and some baseline data were not recorded. We have subsequently improved the data administration procedures. However, in a definitive trial, trial data collection will need to be independent of intervention delivery.

Respondent burden was a key consideration for this participant group and the data collection procedures were designed to minimise this. Nevertheless, the dietary assessment method was weak. We have subsequently used the Dietary Instrument for Nutrition Education (DINE) questionnaire as advised by the National Obesity Observatory for weight management interventions.43 In a definitive trial, the need for a more robust, objective measurement of PA and better dietary assessment will need to be balanced against increased respondent burden.

Intervention delivery and capacity

The intervention design was strengthened by the incorporation of individual and group-based delivery. The one-to-one risk assessment consultations provided opportunities to introduce topics that facilitated motivational interviewing.23 The group-based PA and cookery sessions encouraged social support with mutual encouragement. Group-based sessions are likely to reduce cost and potentially improve the cost-effectiveness of the intervention.44 Positioning the intervention within leisure services helped to avoid ‘medicalising’ the problem and enabled a variety of PAs to be provided. The trainers were accessible to the participants on a casual basis, both during the 10-week programme and after its completion, as they were regularly present in the leisure centres with other groups. The trainers encouraged participants to make independent use of leisure centre facilities and join mainstream activity classes. New mainstream classes were introduced in response to the requirements of NLNY participants, some of whom invested in their own access to leisure service cards after completing follow-up at 12 months. The local leisure centre continued to provide a meeting point for participants post follow-up. The standard (Register of Exercise Professionals) training programmes for fitness trainers provided a good foundation for intervention delivery, which we enhanced with extra training in motivational interviewing and good clinical practice. Similar delivery capacity would be available in other areas of the UK by utilising staff trained to deliver fitness programmes, such as within local authority leisure services.

Intervention cost

In this study, we focused on developing an engaging intervention and sustainable administration procedures. Group sessions were used to maximise efficiency. Funding provision was appropriate for a developmental project and further cost savings are being explored in refining the service model. Economic evaluation of the NLNY service model will be undertaken as part of a definitive trial.

Sample size

This feasibility study has provided data that will inform sample size estimation for a definitive trial and show how the NLNY intervention performs in comparison to interventions used in previous trials: for example, in NLNY, 21% of participants lost ≥5% of their body weight at 12 months of follow-up; the equivalent value in EDIPS was 38%.6 A comparison of reductions in the waist circumference will also be informative.45 ,46

Strengths and weaknesses in relation to other studies

In planning the NLNY intervention, we were able to draw on the experience of EDIPS-Newcastle as previously described.27 The efficacy evidence for lifestyle, diet and PA interventions to prevent T2D has been tested in research settings.3 Although it is difficult to compare across studies with different participant gender distributions and baseline levels for the outcome variables of interest, it appears that weight loss observed at 12 months in this pilot study (mean 5.7 kg men, 2.8 kg women and 4.3 kg overall) was comparable to that achieved in the Finnish DPS (mean 4.2 kg) and more than in EDIPS-Newcastle (mean 2.3 kg). Similarly, it appears that the reduction in waist circumference (mean 7.2 cm men, 6 cm women and 6.6 cm overall) was more than in the Finnish DPS (mean 4.4 cm) and EDIPS-Newcastle (mean 1.7 cm).12 ,27 In the International Day for the Evaluation of Abdominal Obesity (IDEA) study, waist circumference was shown to be a better predictor than BMI of diabetes and cardiovascular disease.46

Some countries have already implemented large-scale diabetes prevention programmes for high-risk groups. Finnish national diabetes prevention program (FIN-D2D) and GOAL were both conducted in Finland,47–49 and a state-wide primary prevention programme has been implemented in Saxony in Germany.8 The Australian ‘Life!’ Study in Victoria State was developed with a direct recruitment strategy, underpinned by social marketing and developed from the Greater Green Triangle Translational study.50 ,51 These programmes did not achieve the same degree of weight change as the DPP and DPS. The DPP and DPS included supervised group PA sessions within their protocols, but service provision models have relied mainly on classroom-based counselling.8 The alternative approach used here may be more effective, especially for hard-to-reach groups. Provision of the 12 month free access to leisure card increased the cost of the intervention and this may make the NLNY intervention inefficient or difficult to afford. The commissioners are considering alternatives such as subsidised service access for continued implementation.

Recruitment in previous diabetes prevention trials has relied on assessment of IGT using an oral glucose tolerance test. This is not practical for service provision3 and large-scale prevention programmes have used risk scoring methods.52 Blood testing is required to exclude undiagnosed T2D, but was not included in the NLNY pilot. Addressing this limitation will be important prior to a definitive trial. The most convenient procedure would be a risk score screening together with a simple blood test (such as point of care HbA1c followed by venous blood testing for those with high risk to exclude T2D).5

Importance of the study: possible mechanisms and implications for clinicians or policymakers

The NLNY feasibility study has demonstrated successful recruitment and retention, the feasibility of collecting individual level outcome data within a service model, and likely effectiveness to change behavioural and intermediate health outcomes.

The NHS Health Checks programme in England offers simple tests including BMI and, where appropriate, HbA1c to adults aged between 40 and 74 years.38 NICE guidance advocates lifestyle intervention for T2D prevention linked to NHS Health Checks.3 Delivery capacity is a major consideration in planning service provision for diabetes prevention. By citing the NLNY intervention within local authority leisure services, we have utilised appropriate and available facilities together with the expertise of existing trained staff. This study demonstrates the feasibility of an intervention model, delivered by fitness trainers in leisure and community settings with collection of robust outcome data. This model has potential for scalable service provision.

Future research

The outcome data reported here are encouraging and the next step is a formal test of effectiveness and cost-effectiveness in a definitive trial prior to translation for mainstream practice. The results of a qualitative process evaluation of participants’ perspectives of their behavioural change53 provide further evidence to complement the findings reported here on feasibility, acceptability and potential effectiveness.


High retention and positive outcomes at 12 months are encouraging indications of the potential success of the NLNY intervention. A controlled trial with assessment of cost-effectiveness is warranted. The intervention provides a potential model for sustainable service provision in the UK and is scalable.


The authors would like to thank the participants and all the staff who helped with the study. The study was funded by a consortium including Sport England; Middlesbrough Primary Care Trust; Public Health North East; and Middlesbrough Council. The authors wish to thank Diabetes UK for their input to the Steering Group. In 2012, London hosted the Olympic and Paralympic Games. The aspiration that the Games would encourage greater participation in physical activity inspired the development of the ‘New life, New You’ (NLNY) intervention for T2D prevention as a health and sports sector partnership and the project was awarded the 2012 ‘Inspire’ mark. We acknowledge the contribution made by local organisations in planning this intervention in connection with the Olympic and Paralympic legacy.



  • Contributors MW was a member of the Steering Group responsible for securing funding and for the outline plan for the NLNY intervention and evaluation. LP contributed to the development of the NLNY pilot intervention, designed the pilot evaluation and the qualitative study, and conducted the qualitative interviews. VR conducted the statistical analyses. MW and VR reviewed and contributed to the manuscript drafted by LP. All authors read and agreed on the final version.

  • Funding Middlesbrough Council; Middlesbrough Primary Care Trust; Public Health North East, Sport England. Newcastle University, Institute of Health and Society provided funding for open access publication.

  • Competing interests The business case and outline plan for this pilot study was determined by a steering committee. This included representatives from members of the organisations that comprised the funding consortium as well as the Principal Investigator for the evaluation, co-author MW. The detailed development of the intervention was then progressed by a small operational team including the evaluation researcher, co-author LP. The operational team reported to the steering committee. The funders had no role in the collection, analysis and interpretation of data, writing of the article or in the decision to submit it for publication. MW, VR, and LP receive salaries from Newcastle University, Institute of Health and Society that provides open access funding for the publication.

  • Ethics approval Newcastle University Ethics Committee.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement No additional data are available.