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临床试验/NCT02845791
NCT02845791已完成不适用

Prevention Strategies for Adolescents at Risk of Diabetes - A Randomised Controlled Trial of an Interactive Family-based Lifestyle Programme

University Hospitals, Leicester2 个研究点 分布在 1 个国家目标入组 318 人开始时间: 2016年7月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
318
试验地点
2
主要终点
The primary endpoint is to detect a change in objectively measured MVPA of 10 minutes per day within the intervention group at 6 months.

研究概览

简要总结

To investigate whether the interactive family based lifestyle programme leads to behaviour change at 6 months with the primary outcome being increased levels of moderate to vigorous physical activity (MVPA).

详细描述

To investigate whether the lifestyle programme results in changes to the following outcomes 3 and 6 months after baseline assessment (Child)

  • An increase in objectively measured total amount of physical activity
  • An increase in the proportion meeting MVPA guidelines (measured objectively)
  • Reduction in time spent sedentary (measured objectively and self-reported)
  • Change in self-reported physical activity
  • Reduction in measures of adiposity (body mass index percentile, per cent body fat)
  • Improvement in psychological factors that may mediate physical activity participation (self-efficacy, motivation, attitudes, social support and enjoyment of physical activity; and physical self-perceptions)
  • Change in healthy food provision and parenting practices for healthy food
  • Improvement in diet composition.
  • Improvement in knowledge of physical activity and nutrition.
  • Improvement in cardio-metabolic variables (blood pressure, glucose, HbA1c, cholesterol)

The Investigators will also include qualitative data collected from:

  • Evaluation forms following each intervention workshop session which will be completed by the Parent/guardian, child and facilitator
  • Feedback from focus groups to be held following completion of the total intervention i.e. 8 sessions

To investigate whether the lifestyle programme results in changes to the following outcomes 3 and 6 months after baseline assessment (Parent(s)/guardian(s))

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
12 Years 至 14 Years(Child)
性别
All
接受健康志愿者

入选标准

  • Parents/guardians will answer questions in the eligibility questionnaire about their child and family health history. Participants will be invited to participate if they are 12-14 years old inclusive (12 years 0 days to 14 years 354 days old) and are identified as having the following risk factors for development of Type 2 Diabetes (which will be identified from the eligibility questionnaire):
  • BMI > 95th percentile for age and gender OR
  • BMI > 85th percentile PLUS one other from the following list:
  • Family history of Diabetes (first degree relative).
  • Non-white ethnicity.
  • Watching TV/play computer games for more than 2 hours a day (self-report).
  • Sugar intake more than 1.5 cans (or 532 ml) of fizzy pop/fruit juice per day (self-report).

排除标准

  • Young people will not be eligible for participation in the study if they are outside the age range of interest (<11 years and 364 days or >14 years and 1 day), have an existing diagnosis of Type 1 or Type 2 Diabetes, < 85th percentile. Young people will also be excluded if they themselves do not provide written assent or their parent/guardian does not provide written consent.

研究组 & 干预措施

Control

No Intervention

The control participants will not receive the educational intervention but will be provided with a detailed advice leaflet for themselves and their parents/guardians.

Intervention

Other

The educational intervention participants will receive the eight 90 minute sessions of an interactive family based lifestyle programme.

干预措施: Interactive Lifestyle programme workshop (Behavioral)

结局指标

主要结局

The primary endpoint is to detect a change in objectively measured MVPA of 10 minutes per day within the intervention group at 6 months.

时间窗: 6 months post baseline

Participating children and adults will be asked to wear the wrist worn GENEActiv accelerometer (ActivInsights, Kimbolton, Cambridgeshire, UK) continuously for up to 8 days.

次要结局

  • An increase in total volume of physical activity(3 and 6 months)
  • Improvement in HbA1c(3 and 6 months)
  • Reduction in time spent sedentary(3 and 6 months)
  • Change in physical activity levels(3 and 6 months)
  • Improvement in Triglycerides(3 and 6 months)
  • Blood Pressure (Child)(3 and 6 months)
  • Improvement in Total Cholesterol(3 and 6 months)
  • Improvement in HDL-C(3 and 6 months)
  • An increase in the proportion meeting MVPA guidelines(3 and 6 months)
  • Improvement in diet composition(3 and 6 months)
  • Improvement in cardio-metabolic variables(3 and 6 months)
  • Reduction in Body mass index percentile (BMI)(3 and 6 months)
  • Change in healthy food provision and parenting practices for healthy food(3 and 6 months)
  • Improvement in knowledge of physical activity and nutrition(3 and 6 months)
  • Improvement in Glucose(3 and 6 months)
  • Blood Pressure (Parent(s)/guardian(s))(3 and 6 months)

研究者

发起方
University Hospitals, Leicester
申办方类型
Other
责任方
Sponsor

研究点 (2)

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