The effect of a multi-disciplinary obesity intervention compared to usual practice in those ready to make lifestyle changes: design and rationale of Whanau Pakari
© Anderson et al. 2015
Received: 18 November 2014
Accepted: 21 September 2015
Published: 8 October 2015
Child obesity internationally has been identified as one of the major threats to future population health. Indigenous people and those from lower socio-economic backgrounds are over-represented in obesity statistics. There is a need for evidence of effect of interventions for child obesity with long-term follow-up. Whether engaging with those that are more motivated to make lifestyle changes is a useful strategy has not been fully explored. We hypothesise that in obese/overweight children, assessed as psychologically “ready for change”, delivery of a 12-month multi-disciplinary intervention programme results in a significant reduction in body mass index standard deviation score.
Whanau Pakari is an unblinded randomised controlled clinical trial comparing a 12 month intervention programme with standard practice, with 6 monthly assessments for 2 years, conducted in Taranaki, New Zealand (a region where 15.8 % of the population are indigenous). It specifically targets indigenous people and those in more deprived households.
Obese/overweight children and adolescents aged 5–16 years are eligible. Exclusion criteria are medical/psychological conditions leading to inability to undertake physical activity/participate in group sessions; those not “ready” to make lifestyle changes; and those without a committed family member.
Assessments of health parameters, dietary history, physical activity and overall health-related quality of life/psychological functioning are completed in the participant’s home. Fasting blood tests are obtained at baseline, 12 and 24 months.
The primary outcome is body mass index standard deviation score. Secondary outcomes include quality of life, dietary behaviour and physical activity, cardiovascular and metabolic profile (blood pressure, resting heart rate, waist circumference), glycaemic control (fasting glucose and glycated Haemoglobin), fasting insulin, and lipids.
A general linear mixed model will be used to assess change from baseline using the 6, 12, 18 and 24 month measures, adjusting for age, gender, socioeconomic status and ethnicity, and whether at the contemplative or preparation/action stages of readiness for change.
This trial will inform the development of management programmes for obese children and adolescents that are appropriate for indigenous populations. It will investigate whether those at the preparation/action stage of “readiness” to make lifestyle changes are more successful in making changes than those who are contemplative.
Australian New Zealand Clinical Trials Registry (ANZCTR):12611000862943. (Date registered 15/08/2011).
KeywordsPediatric Obesity Research methods Indigenous people Whanau Pakari Intervention studies Randomised controlled trials Nutrition Physical activity Body mass index
Childhood obesity causes substantial morbidity, mortality and health cost [1, 2]. The rapid increases in the proportion of the population that are overweight and obese are now apparent in children as well as adults in both developed and developing countries [1, 3]. New Zealand has not avoided the global obesity epidemic, with the country now being ranked fourth in the Organisation for Economic Cooperation and Development (OECD) rankings for overweight and obesity (65 % of the population over 15 years are classed as either overweight or obese) . The Health of New Zealand Children Survey 2013/2014 reported 10 % of children aged 5–14 years are obese, up from 8 % in 2006/2007 . Rates of obesity are higher for Maori – New Zealand’s Indigenous population (15 %), Pacific Island children (25 %), and children living in the most deprived quintile of households (18 %) .
Few children and adolescents struggling with weight issues have access to intervention programmes. In New Zealand, most overweight or obese children and adolescents coming to the attention of medical professionals are either managed by a general practitioner or general paediatrician with minimal intervention programmes being available nationally . No national cohesive approach for managing childhood obesity exists, despite national clinical guidelines being available since 2009 . A recent multi-centre audit showed that, irrespective of type of intervention, a small but significant reduction in BMI SDS was achievable (−0.15 overall), highlighting the importance of health professionals being proactive in identifying and addressing child obesity . However, even when obesity is identified, intervention is infrequently implemented. In Australia, general practitioners were recently shown to provide weight management for <2 % of overweight and obese children attending primary care services , and paediatricians reported lacking confidence in the management of obesity in children, with only 37 % reporting training in the management of obesity-related comorbidities . This is also likely to be the situation in New Zealand, although to date, similar surveys remain unpublished.
Past meta-analyses have supported multi-disciplinary intervention programmes for addressing child and adolescent obesity, as they are deemed as having the greatest chance of success [11, 12]. New Zealand’s Ministry of Health guidelines support an approach of working with family to address food habits, increase physical activity and to promote behavioural change . Evolution of the current trial came from these recommendations, findings from an audit of an existing physical activity/nutrition programme  and recognition of the need to address accessibility for those most affected by obesity. A trial was deemed necessary to ensure future decision-making with regard to child and adolescent obesity was informed by the most reliable evidence possible. The trial has been designed with consideration of the Consolidated Standards of Reporting Trials (CONSORT) 2010 statement .
Theoretical model of stages of readiness for change 
“I do not have a problem”
“I may have a problem”
“I may have a problem and need to do something”
“I will try these changes”
“The changes I have made are now part of what I do”
The transtheoretical model has been used to assess individual’s motivation for smoking cessation , and various tools for readiness for change have been trialled in the obesity setting [17, 18]. The utility of readiness for change remains unclear as it relates to obesity services, and it is too simplistic to expect that every individual would move through these stages in a similar fashion. However, previous studies have highlighted the importance of tailoring interventions to the individual stage of change rather than treating all participants as if they are in preparation or action stages . If there were a quantitative tool that could predict likelihood of success at initial assessment, this would potentially focus health resource where it was most likely to make a difference. Given the complexity of behaviour change as it relates to obesity, the original readiness for change questionnaire  would require modification and expansion to include questions regarding eating behaviour, attitude towards weight and physical activity behaviour. Confidence to make changes in physical activity and eating behaviour would also need to be considered.
The question remains as to whether an individual’s readiness in the “snapshot” situation of an assessment translates to ongoing motivation to make lifestyle changes over time. In the domain of child and adolescent obesity, parental readiness is a vital factor in a child or adolescent’s success in making and maintaining lifestyle changes. If a parent believes their child’s weight is a problem, or that they as parents are overweight, they are more likely to be ready to make lifestyle changes for their child .
It provides a trained roving community coordinator to meet families in their homes, enabling improved access to the clinical service, especially for Maori.
It assesses “readiness for change” both quantitatively and qualitatively.
It provides follow up to 12 months post intervention to assess persistence of lifestyle changes, which is longer than any other multi-disciplinary obesity intervention model trialled in New Zealand.
There is a clear need for evidence-based interventions for child obesity that demonstrate on-going effectiveness . Whether engaging with those that are more motivated to make lifestyle changes is a strategy that warrants further exploration. Our objectives are firstly, to undertake a multi-disciplinary intervention, which is accessible and appropriate for those most affected by child obesity. Secondly, we aim to assess whether a quantitative RFC questionnaire is useful in predicting response to the intervention. We hypothesise that in obese/overweight children, assessed as psychologically “ready for change”, delivery of a 12-month multi-disciplinary intervention programme results in a significant reduction in body mass index standard deviation score at 12 months.
Whanau Pakari is an unblinded randomised controlled clinical trial being conducted in Taranaki, New Zealand (population 23,139 children aged 0–15 years, of which 28 % are Maori) . Ethical approval was granted by the Health and Disability Ethics Committee (Ministry of Health, New Zealand; CEN/11/09/054), and the trial was registered with the Australian New Zealand Clinical Trials Registry (ANZCTR: 12611000862943). Locality approval has been obtained from Sport Taranaki, and the Taranaki District Health Board.
Children from the Taranaki region aged 5–16 years, with a body mass index (BMI) ≥98th centile, or those >91st centile with weight related comorbidities will be offered participation in the trial if referred to “Whanau Pakari”. These cut-offs are a modification of UK Cole data, and have been chosen as they are nationally accepted for use by the Ministry of Health for defining obesity and overweight respectively in the community for 0–5 years [20, 21]. (There are no nationally accepted growth charts or official cut-offs in use for >5 year old children currently.)
Exclusion criteria will be significant medical or psychological conditions leading to inability to undertake physical activity or participate in group sessions; those not “ready” to make lifestyle changes; and those without a committed family member (essential to support the family-based approach of the programme).
Recruitment for the trial will be through the service, which is being advertised across Taranaki through multiple channels, including referrer training half-days (training sessions about the service, and how to have conversations about weight with families), meetings (hui) with all stakeholders, general practice visits, school visits, media releases, pamphlet drops at public places and events, and the Public Health Unit of Taranaki District Health Board.
Whilst the trial will assess a “mainstream” clinical service, the aim is to target Maori and the most deprived in the community. To achieve this aim we will use identified facilitators that enable Indigenous people’s participation such as relationship and partnership building, involvement of Indigenous staff, the use of Indigenous knowledge models (such as He Korowai Oranga: the Maori Health strategy and the Whanau Ora [healthy families] tool) [22, 23], targeted recruitment techniques (such as working with Maori health workers within the community to engage with families) and adapting study material .
All children referred will be seen in the family (whanau) home by the Healthy Lifestyles Coordinator (a health professional trained in focussed weight-related assessment, supported by a Paediatrician). This design aspect allows the trial to run as a community-based service yet with a full clinical component to it. Removal of a hospital-based appointment with a specialist was designed to enable access to the service for larger numbers and minority groups, and to avoid “medicalisation” of the process. Given the service is targeting Maori and those from lower socio-economic areas, ensuring accessibility and appropriateness are crucial to the study design, without compromising clinical care.
Conception and consultation
The multi-disciplinary intervention model was developed after consideration of the national guidelines for implementation of weight management programmes, and the recommendations from the international systematic reviews and meta-analyses [7, 11, 12]. Longer-term follow-up was deemed imperative to determine whether lifestyle changes persisted over time, which has been a deficit of many previous studies. Conceptually, a multi-disciplinary intervention that incorporated dietary, physical and psychological support was considered important, with 12 months the optimal length of intervention. It was necessary for the intervention to be community-based with a strong focus on accessibility to Maori, and those from lower socio-economic areas.
Build appropriate and positive relationships around the region, particularly in South Taranaki, which has a proportionally larger population of Maori.
Ensure acceptability of the intended research by using a community-based approach.
Provide an opportunity for input and contribution from community stakeholders during the consultation process.
This process ensured that potential barriers for engagement for Maori and the most deprived in the community such as lack of access, unfamiliarity with research, distrust and problems with the research material were addressed . The consultation process is ongoing.
Assessment information for all participants
Resting heart rate
Acanthosis nigricans screen
Ear, nose and throat examinationg
Self report of Tanner pubertal stageh
Accompanying adult’s height and weight
BMI, BMI percentile and BMI standard deviation score (SDS) will be calculated using UK Cole normative data  on the uploadable KIGS auxology software (Pfizer Endocrine Care TM). Height percentile will be calculated using gender specific growth charts for 2–18 years recommended by the Australasian Paediatric Endocrine Group for Australian and New Zealand use , based on Centers for Disease Control stature for age and weight for age data . To improve accuracy, BP SDS will be calculated using an age-based paediatric blood pressure reference chart calculator based on data from The Fourth Report [28, 29]. BP SDS will then be converted to percentiles. Peak flow percentile will be calculated based on reference New Zealand peak expiratory flow rates . Waist hip ratio, and waist height ratio (WHtR) will be calculated. Participants will be deemed pubertal if they are female with breast development ≥ B2 or male with pubic hair development ≥ P3 on Tanner pubertal staging . Level of household deprivation will be calculated based on the New Zealand Deprivation Index 2006 .
One aim of this trial is to determine whether there is an association between reported degree of “readiness” to make lifestyle changes at baseline assessment, and improvements in lifestyle, including BMI SDS. Readiness for lifestyle change will be based on the transtheoretical model of stages of change , and will be established with two questionnaires (parent and child/adolescent) and the best judgement of the Healthy Lifestyles Coordinator at the end of the baseline assessments. Both questionnaires will be based on the 12-item Readiness to Change Questionnaire  and will use a 5-point Likert scale to assess the parent’s and child/adolescent’s beliefs, attitudes and behaviour about weight, eating behaviour and physical activity. Given the complexity of obesity, the questionnaires will be expanded. The child questionnaire will have 21-items and will be used for children 11 years and older, and a 27-item parent questionnaire, including 6 questions regarding family attitudes/behaviour, will be administered to parents. Whilst self-efficacy/confidence to make changes are not extensively measured, confidence in making changes in physical activity and eating behaviour has been included in both quantitative questionnaires.
Qualitative assessments of readiness for change will be made by the Healthy Lifestyles Coordinator at the end of the assessment. This will be the Coordinator’s overall subjective opinion as a health professional of stage of change in both the committed family member and child (if >11 years of age), based on the assessment. A qualitative stage of change will be included as this is what is undertaken in current clinical practice, and provides a comparator for the quantitative tool. The quantitative assessment will be scored at point of data entry by the Healthy Lifestyles Coordinator. Cronbach’s alpha will be used to establish the reliability of our readiness for change lifestyle questionnaire. Confirmatory factor analysis will be used to examine convergent and discriminant validity. The questionnaire was tested for understanding and comprehension in a randomly selected cohort of clinic patients prior to trial commencement.
Questionnaires that will be administered to the child/adolescent or parent include the Paediatric Quality of Life Inventory (PedsQL)™ – a measurement model designed to evaluate health-related quality of life in children and adolescents that has been extensively validated [33–38], the Achenbach Child Behavior Checklist (CBCL) (Child Behavior Checklist for Ages 1½-5: 7–28-00 Edition-601, Child Behavior Checklist for Ages 6–18: 6-1-01, Edition-201, Youth Self-report for Ages 11–18: 6-1-01 Edition-501) , children’s physical activity questionnaire (C-PAQ) , modified children’s dietary questionnaire for New Zealand use (CDQ) , 24 h food recall, knowledge of healthy lifestyles questionnaire (modified from the 2008 Nutrition Survey) , and our RFC questionnaire. Any participant deemed not ready for change will be reassessed every six months.
Assessment of physical fitness
Physical fitness assessments include the 550 m walk/run , and 5 days of ActiGraph wGT3X-BT (Actigraph, Pensacola, Florida, USA) accelerometer wear will be requested (3 weekdays and 2 weekend days), giving an estimated reliability of 0.80 in children and 0.70 in adolescents . These levels of reliability have been questioned in more recent studies , however longer wear time is not practical due to resource. Epoch time will be set to 60 s and cut-off time 60 min.
Venous blood sampling will be undertaken to assess for metabolic status (Table 2). These biomarkers identify the biochemical comorbidities associated with obesity [46, 47]. Incentivisation for these samples will be provided.
Weight-related comorbidities will be screened for and referrals will be made where appropriate.
Every child entering Whanau Pakari will be discussed at the multi-disciplinary team meeting, allowing a full clinical review and referrals for further investigation where appropriate, with additional discussion of dietary intake, physical activity, and psychology issues. The assessments and multi-disciplinary meetings will be repeated for each child/adolescent every six months, irrespective of which group they are randomised to.
Home visits with the dietitian and physical activity coordinator in the initial phase
Weekly contact in activity sessions of either physical activity OR
- 3)Psychology sessions (covering topics such as bullying, self-esteem, parenting, making lifestyle changes), and dietitian sessions (covering topics such as portion size, virtual supermarket tours, healthy food on a budget, and vegetable gardens) (Table 3).Table 3
Support provided to each group of trial participants enrolled in Whanau Pakari
Control (Current “standard care”)
6, 12, 18, 24 month assessments with nutrition advice and feedback (blood tests at baseline, 12, 24 months)
Home visit within 1st month from physical activity coordinator and dietitian
Physical activity coordinator/Dietitian review of progress at 6 months (seen at group)
Questionnaire review (team), multi-disciplinary team meeting – review and action of alerts
Weekly activity and education sessions for 12 months
Total home visits over 2 years
The participants will be engaged in the programme one hour per week for four school terms (equating to a total of 40 sessions). The same programme will be delivered to all participants, however these will be tailored to meet the cultural requirements of participants, for example, sessions that include traditional Maori games, recipe makeover of dishes from different cultures, and honouring of particular dietary requirements in cooking sessions. A committed family member will be required to attend to support and learn alongside the child/teenager, as the programme is family-focussed. No incentivisation will be provided for attending sessions. A commitment contract will be signed at entry to the programme, outlining expectations of attendance at a minimum of 70 % of sessions to gain the most out of the programme. After 12 months, families will be linked into local sport centres/aquatic centres/gym facilities.
The non-intervention (control) group will receive the same home-visit model and assessments as the intervention group, but will not undertake any of the intervention sessions (Table 3). The families will receive feedback from the assessments with dietary and physical activity guidelines. This model was chosen for community acceptability and is very similar to what is currently considered ‘standard care’. This group are offered the intervention after 24 months. All participants declining intervention and those who have completed intervention and 12 month follow-up will be discharged back to primary care, with a guideline sheet of what to monitor, and assess with regard to weight-related comorbidities. Any participants withdrawing from the trial before the end of the 24 months will be incentivised to participate in a modified assessment to allow measurement of their progress, thus maximising completeness of data for the intention to treat analysis.
At baseline, there will be 2 assessments of RFC (given it is not known if a quantitative tool will be successful): the clinician’s subjective measure (ranked pre-contemplation, contemplation, preparation/action), and a specifically devised questionnaire using a 5-point Likert scale that is completed by the child (if > 11 years of age) and a second one for the parent. The RFC questionnaire was based on the original readiness to change questionnaire , focussing on beliefs and behaviour around three factors: weight, eating habits and activity levels. If the RFC ranking is scored in the contemplative or further along on either scale, then participants will be offered entry into the trial. We purposely set the bar low (i.e. below the preparation/action level) to assess whether degree of RFC predicts outcomes within those contemplative or above.
Patients will be assessed, consented, and entered into the trial prior to randomisation. Randomisation by minimisation (using age and ethnicity) will be conducted using the Minim randomisation computer programme which maintains approximate balance in the 2 arms for age and ethnicity but incorporates a random element so it cannot be predicted which study arm the subject will be allocated to.
The primary outcome measure is the change in BMI SDS in the intervention group compared with the control group recorded at 6, 12, 18 and 24 months post enrolment.
Secondary outcomes include changes in health-related quality of life; dietary knowledge and behaviour; physical activity (specifically moderate to very vigorous physical activity), sedentary behaviour, knowledge of benefits of physical activity, cardiovascular and metabolic profile (blood pressure, resting heart rate, waist circumference and WHtR) all at 6, 12, 18, and 24 months, and glycaemic control (fasting glucose and HbA1c), fasting insulin and lipids at baseline, 12 and 24 months.
Other aims and outcomes
This study also aims to investigate whether those assessed as ready for change (i.e. preparation/action) experience a greater reduction in BMI SDS compared with those less ready for change (i.e. contemplation). If the intervention is found to be effective, a cost-effectiveness analysis will be undertaken, taking into account multiple outcome parameters.
The Healthy Lifestyles Coordinator will collect all data (apart from physical activity assessments) in the home assessments.
All data from assessments will be entered into a specific purpose-built database, which will be reviewed monthly for data validity and completeness. This database includes alerts for data outside acceptable medical parameters, for example, elevated blood pressure percentiles, for discussion at multi-disciplinary meetings.
Progress will be captured on the multi-disciplinary team meeting database page, so the team can review the results of each 6-month assessment for each participant, and make further recommendations or referrals.
With 107 participants per group (120 to account for a 10 % dropout rate) there is 80 % power to detect a difference in change in BMI of 0.5 SDS at the 5 % level of significance, with a standard deviation of 1.3 . Of note, only 15/54 lifestyle studies included in a systematic review at the time of study design reported power calculations . Subsequent meta-analysis of interventions has shown that even a change of −0.1 BMI SDS can lead to improvements in cardiovascular and metabolic outcomes . It is hoped that even demonstrating smaller differences as this more recent literature has shown will still be important at a population level.
Statistical analyses will be performed using SAS version 9.3 (SAS Institute Inc. Cary NC). A general linear mixed model will be used to assess change from baseline measured at 6, 12, 18 and 24 months after initiating the intervention adjusting for age, gender, socioeconomic status, and ethnicity and degree of readiness for change. Means and standard deviations of changes from baseline in outcomes of interest, for both the raw and modelled data, will be presented.
Baseline characteristics will be summarised using descriptive statistics. Continuous variables will be described as numbers of observed and missing values, mean, standard deviation, median, minimum and maximum. Categorical variables will be described as frequencies and percentages.
Analyses will be performed on the intended to treat population. Reporting will adhere to the CONSORT guidelines for reporting parallel group randomised trials .
Whanau Pakari is expected to provide important new knowledge to the area of child obesity. This will be achieved with its focus on an indigenous group at increased risk for obesity and its resulting comorbidities, and through its engagement with the community to increase acceptability of the programme. It is likely to inform these areas in a robust manner if high participation is achieved and maintained.
This randomised controlled trial is unique in three key ways. First, it is assessing a mainstream multi-disciplinary clinical service that has evolved to specifically ensure accessibility and appropriateness for Indigenous people. Whanau Pakari is a community “real life” intervention programme resulting out of a clinical need, and has the potential to answer critical questions in relation to delivery of interventions in this area. Secondly, Whanau Pakari utilises a home-visit model which replaces hospital medical assessments, therefore “de-medicalising” obesity assessments. The family-based home model is likely to appeal to many ethnic groups who resist the hospital-based mainstream clinical models currently operating in most areas. Thirdly, Whanau Pakari will only include those considered potentially ready for change, and will investigate whether the level of “readiness” to make lifestyle changes predicts improved outcomes in intervention programmes. If the RFC measures provide a reliable and valid measure of outcome success, then the development of paired interventions around motivation for change for those in earlier stages of change followed by direct interventions for those in later stages could result in less programme dropout as well as being a more efficient and cost effective utilisation of limited resource.
A limitation of this study is the use of self-report for Tanner pubertal stage. Previous literature has demonstrated that obese girls tend to overestimate breast size and obese males stage of pubic hair development more than their non-obese counterparts . However, we did not believe it was appropriate to undertake pubertal examination within the home setting, and it was determined this would be a more appropriate cut-off for pre-pubertal and pubertal status than an arbitrary age for males and females.
Weight-related comorbidities are a particular concern in child obesity, given the long-lasting effects of these conditions . Past meta-analysis highlighted that a BMI SDS reduction of −0.1 led to significant improvements in multiple cardiovascular and metabolic outcomes over time . BMI, in conjunction with waist circumference, WHtR, fasting lipids, glucose and insulin, and blood pressure (all being measured at intervals over an extended period of follow-up) will provide a comprehensive assessment of cardiovascular and metabolic outcomes long-term.
Whilst there has been a shifting focus toward early obesity intervention targeting critical periods of human development, there is still a need for an effective intervention programme to provide assistance for those children and adolescents who are already obese. This research aligns with the Ministry of Health’s clinical guidelines for weight management in children and young people , and addresses barriers to accessing services and programmes identified by the Office of the Auditor General’s performance audit into child obesity .
In summary, this trial will determine if this unique multi-disciplinary intervention will result in improved health outcomes, especially among Maori. It will also investigate whether there is an indication that being at the preparation/action stages of RFC compared to those in the contemplative stage results in improved success in intervention programmes. As translational research, it will inform the New Zealand Ministry of Health regarding ways to combat child and adolescent obesity. It is hoped this study will lead to prevention of the adult associated comorbidities of child obesity into later life for some individuals, thereby reducing morbidity, particularly for those most vulnerable in our population.
Australian New Zealand Clinical Trials Registry
Organisation for Economic Cooperation and Development
Consolidated Standards of Reporting Trials
Readiness for change
Body mass index
standard deviation score
Waist height ratio
- Peds QL:
Pediatric Quality of Life
Child Behaviour Checklist
Children’s Physical Activity Questionnaire
Children’s Dietary Questionnaire
This trial is funded by grants from the Health Research Council of New Zealand, Taranaki Medical Foundation, Royal Australasian College of Physicians, Maurice and Phyllis Paykel Trust, and Lotteries Health Research. We would like to acknowledge Dr Katharine Treves and Michelle Butler, who will assist with data collection and entering; Diana O’Neill and Dr Pat Tuohy (Ministry of Health) for their support of the trial; and the Taranaki District Health Board and Sport Taranaki for funding the service. Quality of Life in this paper will be assessed using the PedsQL™, developed by Dr. James W. Varni.
Health Research Council of New Zealand, Taranaki Medical Foundation, Royal Australasian College of Physicians, Maurice and Phyllis Paykel Trust, and Lotteries Health Research.
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