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Comparing levels of physical activity in children with and without type 1 diabetes

Audrie Lim, Charles Stewart
Physical activity has known health benefits in children and young people, and those with type 1 diabetes may benefit additionally from improved glycaemic control. However, there is anxiety over the perceived negative effects of exercise, especially hypoglycaemia. This study compared levels of physical activity in children with and without type 1 diabetes. Participants were asked to fill in a validated physical activity questionnaire adapted for use in the UK. Children with diabetes, in particular girls, were found to be less active than those without the condition. These findings and their implications are discussed in this article.

Publisher’s note: Click here to download Appendix 1.

Physical inactivity has been described as the biggest public health problem of the 21st century, with obesity rates among 10-year-olds in the UK rising from 1.7% in 1974 to 19.1% in 2015 (Blair, 2009). Today, approximately a third of children are either overweight or obese (Stamatakis et al, 2005; Health and Social Care Information Centre, 2015). Despite the benefits of exercise, children’s physical activity (PA) often fails to meet recommended levels (Bélanger et al, 2011).

In response to this pandemic, the World Health Organization (2011) has made global recommendations for activity levels in children, and these have been adopted by the UK Government (Department of Health, 2011). These include moderate to vigorous PA for at least 60 minutes, and up to several hours, every day in all children.

In children with chronic health conditions, there is anxiety over perceived negative effects of exercise that, coupled with low expectations, often result in further restriction of activity (Riner and Sellhorst, 2013; Dantas et al, 2014; Santos-Silva et al, 2014). In type 1 diabetes, this negative perception, especially the fear of hypoglycaemia, exists and may be a contributory factor to low participation rates and a higher prevalence of obesity (Kowalski et al, 2004; Wolfsdorf, 2005). Studies have shown that children with type 1 diabetes derive the same benefits from exercise as any other child, and in addition demonstrate improved glycaemic control (Massin et al, 2005; Quirk et al, 2014; Zebrowska et al, 2014). With individualised participation plans under qualified supervision, exercise should be a safe and rewarding experience (Wolfsdorf, 2005).

Despite being encouraged by the NICE (2015) guideline, PA levels in children with type 1 diabetes have not, to the authors’ knowledge, been assessed previously, and PA promotion does not form a significant part of regular health screening in diabetes clinics. Therefore, in this study, we aimed to compare levels of PA in children with and without type 1 diabetes. Our secondary aim was to compare BMI in the two groups.

Methods
Participants
Children between the ages of 7 and 17 years were eligible to participate. Children with type 1 diabetes were recruited from May to August 2016 from a paediatric diabetes clinic in a London teaching hospital. Clinics were attended by an investigator, who distributed patient information leaflets to children and their parents or carers detailing the study. The patient information leaflets were age-appropriate in their content.

If participation was agreed, written consent was obtained and a PA questionnaire was provided for completion by the children while waiting for their clinic. The investigator remained available to provide assistance upon request.

The control group of children without diabetes was recruited from one primary and one secondary school in Monmouthshire. The same consent was obtained.

The children with type 1 diabetes recruited to the study attended different schools over a wide area, making a truly representative control group impossible to obtain. Due to the disparate nature of the study group, the main criteria for the selection of the control group was not proximity to the clinic but an interest in child healthcare research ideals and the willingness of children, parents and administrative staff to engage with researchers.

Ethical approval
This study was conducted with the approval of the NHS Health Research Authority (16/LO/0723), as well as the local research and development committee, which gave protocol ratification. Informed consent was obtained from the parents or legal guardians of participants under 16, with the option for participants to also give their consent. Two participants, aged 16 and 17, gave their consent independently.

Physical activity questionnaire
We used the Physical Activity Questionnaire (PAQ), a self-report questionnaire developed by Kowalski et al (2004) to measure PA in children. The PAQ comprises nine validated questions relating to PA undertaken in the previous week and is designed for school-age children and young people. Each question is scored out of five and a final score is calculated as the mean of all nine responses; higher scores indicate higher activity.

The original questions were validated for a Canadian population and so minor revisions were made in terms of sporting activities and phrasing to adjust for cultural and sporting preferences in the UK. In particular, question 1 lists 22 sports that respondents are asked to quantify involvement in over the preceding week; in place of floor hockey, street hockey, ice hockey, ice skating, baseball and Canadian football, we inserted tennis, athletics, cricket, rugby, martial arts and gymnastics. Previous studies conducted in the UK and other countries have shown that the revision of questions to suit the local population provides satisfactory results and validity (Janz et al, 2008; Bervoets et al, 2014; Thomas and Upton, 2014; Aggio et al, 2016).

Questions 2–8 relate to activity at specific times of the day and question 9 asks how often PA was performed for each day of the preceding week. The same revised questionnaire was used for all participants, with slight graphic design differences between the 7–11 and 11–17 age groups. The two versions of the revised PAQ are in Appendix 1 (click here to access).

Analysis
Basic demographics, final PAQ activity scores and the types of sports practised were calculated and analysed. To determine the statistical significance between the PAQ responses of the two groups, a two-sample t-test was used. This statistical analysis was also carried out for the comparison of various subgroups (boys, girls, younger children, adolescents, and PA during and after school hours).

We also measured height and weight for both groups to calculate BMI. t-tests were conducted to investigate the potential differences between the BMI results of children with and without type 1 diabetes.

Results
A total of 31 children with type 1 diabetes and 65 without the condition were entered into the study. The population characteristics for the two groups are presented in Table 1. Overall, the group with diabetes was less active than the group without the condition, with an average PAQ score of 2.74 compared with 3.08 (P=0.038).

As can be seen in Table 2, girls with diabetes were less active than those without the condition (PAQ scores 2.33 vs 2.91; P=0.003). There was no difference between the groups when comparing the PA of boys (P=0.197), children (P=0.075) or adolescents (P=0.400).

We analysed the data to compare activity levels during and after school. No significant difference was found between the groups for PAQ questions 2, 3 and 4, which relate to school-time activity (PAQ scores 3.39 vs 3.58 in the diabetes group vs the non-diabetes group, respectively; P=0.370). There was, however, a significant difference in activity after school in those with diabetes compared to those without the condition, as measured by PAQ questions 5, 6, and 7 (mean score 2.54 vs 3.02; P=0.02).

All activities and sports practised in the week leading up to PAQ completion are listed in Table 3. Overall, the five most popular sports were lacrosse (practised by 97% of the total cohort), badminton (93%), volleyball (90%), rollerblading (90%) and hockey (87%). In the group of children with diabetes, hockey, netball and martial arts were the joint fifth most popular sports, whereas in children without diabetes, volleyball and netball came joint fifth.

We aimed to compare BMIs for all participants; however, this was not possible for the primary school-age children in the control group as the necessary equipment was unavailable. We therefore restricted the BMI comparison to children aged 11–17 years. In this age group, there was no significant difference in BMI between the groups (P=0.903; Table 4). There were no significant differences in the BMIs of girls (P=0.562) or boys (P=0.420) with and without diabetes.

Discussion
The benefits of exercise include cardiovascular health, muscle and bone strengthening, psychological and social wellbeing, skill attainment and weight control (Janssen and Leblanc, 2010; Okely et al, 2012). Children with chronic conditions stand to gain as much, if not more, from exercise as otherwise healthy subjects (Wolfsdorf, 2005; Riner and Sellhorst, 2013); however, they face barriers that arise from a fear of “overdoing it” and a misunderstanding of what exercise entails (Thornton, 1997).

In an era where activity rates are deemed generally low, England is ranked joint 34th out of 38 countries according to The Global Matrix 2.0 on Physical Activity for Children and Youth (Tremblay et al, 2016). Intuitively, in light of such poor levels of PA in the general population, expectations in children with chronic illness would be low (Wilkie et al, 2016).

Our results indicate that children with type 1 diabetes are significantly less active than those without diabetes, despite the benefits of exercise described, plus the added advantage of increased insulin sensitivity and reduced HbA1c (Health and Social Care Information Centre, 2015; Massin et al, 2005).

Arguably, there is more PA-related anxiety associated with type 1 diabetes than with other chronic conditions because of the fear of hypoglycaemic events. This fear plays a significant role in the mindset of carers and may contribute to lower PA rates (Brazeau et al, 2008).

Although there was no significant difference between the two groups during school time, PA was found to be significantly lower in the diabetes group after school. School PA includes programmed play, and these results suggest that parents are allowing children with type 1 diabetes to participate in games classes. These children are also active in spontaneous PA during school time, which suggests that they want PA in their daily routine. After school, however, something changes and PA levels become significantly lower in children with diabetes. For most children, especially in the early years, parents have a strong influence on extracurricular activity, and it must be considered that discouragement originating from parents, whether voiced or otherwise, may be a factor in the low out-of-school PA levels in children with diabetes.

BMI was not significantly different between the groups, which is not surprising as the PAQ, while providing good consistency, does not assess duration or intensity of activity and cannot reliably inform on fitness levels (Janz et al, 2008). This does not reduce the relevance of the PAQ, as recent studies have indicated that activity is a more important single variable than obesity in overall health (Ekelund et al, 2015).

Concerns over exercise-induced hypoglycaemia remain controversial. Hypoglycaemia accounts for up to 4–10% of deaths in people with type 1 diabetes (Seaquist et al, 2013), although there are no published cases of deaths occurring during PA due to hypoglycaemia. Overall, the risk for children with type 1 diabetes undertaking PA is deemed to be small (Burr, 2012). Accordingly, NICE (2015) and the American Diabetes Association (2013) support exercise in children, although it would be unwise to ignore the phenomenon of hypoglycaemia completely. During exercise, the sequence of body processes leading to glucose supply and removal from the bloodstream is intricate and will never be precisely mirrored with exogenous insulin regimens or novel delivery systems. In addition, the “after burn” effect of higher-than-normal energy consumption following moderate- to high-intensity PA can be sustained for 24 hours and potentially cause episodes of delayed hypoglycaemia.

In order to remain safe, PA in children with type 1 diabetes needs careful planning with provision of individually tailored advice on nutrition and insulin requirements. This would ideally be supplied at routine diabetes clinic reviews, aided by a physician with an interest in sports and exercise medicine. Support and literature detailing local sports clubs and activity groups should also be made available, with locally provided sports introduction classes offered to break down apprehension and misconceptions about PA.

Our study found that girls with type 1 diabetes exercised significantly less than those without the condition, whereas there was no significant difference between groups in boys. It is widely known, both in the UK and worldwide, that boys engage in PA more than girls at almost every age range (Sherar et al, 2007). As a result, sports participation initiatives for girls have been set up in many countries. “This Girl Can” is an example of one such initiative in the UK. However, it is not clear why girls with type 1 diabetes have fallen behind boys when it comes to exercising as much as their peers without the condition. Whether girls with diabetes are regarded as particularly vulnerable to the perceived ill effects of exercise or whether traditional biological, psychological, social and environmental factors play a significant role needs to be clarified (Sallis, 1995; Telford et al, 2016). We were unable to demonstrate a significant difference in PA between children with type 1 diabetes and controls in the 7–11 and 12–17-year age groups.

Study limitations
This study had a relatively small sample size and further research is required, with more participants, to confirm these findings.

Self-reporting questionnaires are commonly used in sports and exercise medicine, and have been successful, in part, because of their simplicity. As with the PAQ, however, limitations exist. Children with higher PA levels may be more likely to volunteer to participate, and exaggeration may take place due to the natural tendency towards self-promotion. Despite this, the PAQ has demonstrated moderate validity and reliability, and has been extensively utilised in research (Kowalski et al, 2004).

Conclusions
Falling levels of activity in children are a global concern, and children with type 1 diabetes seem particularly susceptible to this trend. Active intervention to increase PA levels in children with diabetes, with a particular focus on girls and after-school activity, should be provided by a multidisciplinary team engaging the whole family. Further work should be extended to other groups of children with chronic illness to ensure that the many benefits of PA are experienced by all.

REFERENCES:

Aggio D, Fairclough S, Knowles Z, Graves L (2016) Validity and reliability of a modified English version of the physical activity questionnaire for adolescents. Arch Public Health 74: 3–11
American Diabetes Association (2013) Sports and recreation. ADA, Arlington, VA, USA. Available at: http://bit.ly/1DmR6TT(accessed 23.08.17)
Bélanger M, Casey M, Cormier M et al (2011) Maintenance and decline of physical activity during adolescence: insights from a qualitative study. In J Behav Nut Phys Act 8: 117–25
Bervoets L, Van Noten C, Van Roosbroeck S et al (2014) Reliability and Validity of the Dutch Physical Activity Questionnaires for Children (PAQ-C) and Adolescents (PAQ-A). Arch Public Health 72: 47–53
Blair SN (2009) Physical inactivity: the biggest public health problem of the 21st century. Br J Sports Med 43: 1–2
Brazeau AS, Rabasa-Lhoret R, Strychar I, Mircescu H (2008) Barriers to physical activity among patients with type 1 diabetes. Diabetes Care 31: 2108–9
Burr JF (2012) Physical activity in type 1 diabetes mellitus. Assessing risks for physical activity clearance and prescription. Can Fam Physician 58: 533–5
Dantas FM, Correia MA Jr, Silva AR et al (2014) Mothers impose physical activity restrictions on their asthmatic children and adolescents: an analytical cross-sectional study. BMC Public Health 14: 287 
Department of Health (2011) Start Active, Stay Active: Report on physical activity from the four home countries’ Chief Medical Officers. DH, London. Available at: http://bit.ly/2vfvcjo (accessed 23.08.17)
Ekelund U, Ward HA, Norat T et al (2015) Physical activity and all-cause mortality across levels of overall and abdominal adiposity in European men and women: the European Prospective Investigation into Cancer and Nutrition Study (EPIC). Am J Clin Nutr 101: 613–21 
Health and Social Care Information Centre (2015) National Child Measurement Programme – England, 2014–15 School Year. HSCIC, Leeds. Available at: http://bit.ly/2v5VS9W (accessed 23.08.17)
Janssen I, Leblanc AG (2010) Systematic review of the health benefits of physical activity and fitness in school-aged children and youth. Int J Behav Nutr Phys Act 7: 40
Janz KF, Lutuchy EM, Wenthe P, Levy SM (2008) Measuring activity in children and adolescents using self-report: PAQ-C and PAQ-A. Med Sci Sports Exerc 40: 767–72
Kowalski KC, Crocker PR, Donen RM (2004) The Physical Activity Questionnaire for Older Children (PAQ-C) and Adolescents (PAQ-A) manual. University of Saskatchewan, Saskatoon, SK, Canada 
Massin MM, Lebrethon MC, Rocour D et al (2005) Patterns of physical activity determined by heart rate monitoring among diabetic children. Arch Dis Child 90: 1223–6
NICE (2015) Diabetes (type 1 and type 2) in children and young people: diagnosis and management [NG18]. NICE, London. Available at: www.nice.org.uk/guidance/ng18 (accessed 23.08.17)
Okely T, Salmon J, Vella S et al (2012) A Systematic Review to Update the Australian Physical Activity Guidelines for Children and Young People. Australian Government Department of Health, Canberra, ACT, Australia
Quirk H, Blake H, Tennyson R et al (2014) Physical activity interventions in children and young people with type 1 diabetes mellitus: a systematic review with meta-analysis. Diabet Med 31: 1163–73 
Riner WF, Sellhorst SH (2013) Physical activity and exercise in children with chronic health conditions. J Sport Health Sci 2: 12–20
Sallis J (1995) A behavioral perspective on children’s physical activity. In: Cheung L, Richmond JB (eds). Child Health, Nutrition and Physical Activity. Human Kinetics, Champaign, IL, USA: 125–38
Santos-Silva R, Melo C, Gonçalves D et al (2014) Comparison between exercise performance in asthmatic children and healthy controls – Physical Activity Questionnaire application. Rev Port Pneumol 20: 138–45 
Seaquist ER, Anderson J, Childs B et al (2013) Hypoglycemia and diabetes: a report of a workgroup of the American Diabetes Association and the Endocrine Society. Diabetes Care 36: 1384–95
Sherar LB, Esliger DW, Baxter-Jones AD, Tremblay MS (2007) Age and gender differences in youth physical activity: does physical maturity matter? Med Sci Sports Exerc 39: 830–5 
Stamatakis E, Primatesta P, Chinn S et al (2005) Overweight and obesity trends from 1974 to 2003 in English children: what is the role of socioeconomic factors? Arch Dis Child 90: 999–1004
Telford RM, Telford RD, Olive LS et al (2016) Why are girls less physically active than boys? Findings from the LOOK longitudinal study. PLoS One 11: e0150041
Thomas EL, Upton D (2014) Psychometric properties of the Physical Activity Questionnaire for Older Children (PAQ-C) in the UK. Psychol Sport Exerc 15: 280–7
Thornton J (1997) Overcoming “protected child syndrome”: kids, exercise, and chronic illness. Phys Sports Med 25: 97–100 
Tremblay MS, Barnes JD, González SA et al (2016) Global Matrix 2.0: report card grades on the physical activity of children and youth comparing 38 countries. J Phys Act Health 13(Suppl 2): 343–66
Wilkie H, Standage M, Sherar L et al (2016) Results from England’s 2016 Report Card on Physical Activity for Children and Youth.J Phys Act Health 13(Suppl 2): S143–9 
Wolfsdorf JI (2005) Children with diabetes benefit from exercise. Arch Dis Child 90: 1215–7 
World Health Organization (2011) Global Recommendations on Physical Activity for Health. WHO, Geneva, Switzerland. Available at: http://bit.ly/1Tkli64 (accessed 23.08.17)
Zebrowska A, Sikira M, Jarosz-Choot P et al (2014) The effects of energy intake, insulin therapy and physical activity on glucose homeostasis in children and adolescents with type 1 diabetes mellitus. In: Szablewski L (ed) Glucose Homeostasis. InTech, Rijeka, Croatia: 71–94

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