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临床试验/NCT04879758
NCT04879758Unknown不适用

The Effect of Communicating Genetic Risk of Type 2 Diabetes and Wearable Technologies On Objectively Measured Behavioral Outcomes: A Randomized Controlled Study

The University of Hong Kong1 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2021年7月7日最近更新:
适应症

试验速览

阶段
不适用
入组人数
150
试验地点
1
主要终点
Changes in Fairly Active Minutes between baseline and 4-week post-intervention, and between baseline and 6-month follow-up

研究概览

简要总结

This study aims to determine the effects of communicating genetic risk for type 2 diabetes (T2D) alone or in combination with goal setting and prompts from a wearable device on objectively measured physical activity (PA) and sedentary behavior (SB) in East Asians. It is hypothesized that this combination will lead to significant favorable changes in objectively measured PA and SB, and that such changes will be more likely to be sustained over 6-month follow-up.

This study aims to recruit 150 healthy East Asian adults in Hong Kong. At baseline, participants will be invited to visit the research laboratory for measurement of a series of variables including height, body weight, blood pressure and grip strength. Participants will also be invited to complete a set of questionnaires to assess their self-reported PA and SB, fruit and vegetable consumption, smoking status and psychological variables. Blood samples will be collected to analyze key diabetes and cardiovascular disease biochemical markers as well as their estimated genetic risk of T2D. Each individual's unique genetic risk for T2D will be estimated on the basis of established genetic variants associated with T2D specifically for East Asians. Each participant will be asked to wear a Fitbit Charge 4 tracker, an objective activity monitoring device, throughout the entire trial.

Participants will be randomly allocated into 3 groups: 1 control and 2 intervention groups. A control group will receive an e-leaflet containing general lifestyle advice for prevention of T2D. An intervention group will receive an estimated genetic risk of T2D, in addition to the e-leaflet. The other intervention group will have a Fitbit step goal set 10% higher than their baseline step count and use prompt functions of the Fitbit tracker, in addition to the genetic risk estimate and e-leaflet.

Activity data from the Fitbit will be collected at 4-week post-intervention; information about lifestyle and psychological variables will be assessed through the questionnaires at both immediate and 4-week post-intervention. To determine the longer-term effect of the intervention, participants will be asked to visit the research laboratory 6 months after the intervention to repeat the same set of assessments as baseline, except the blood samples collected at 6-month follow-up are used only to analyze cardiometabolic risk profiles (not genetic risk). Activity levels will also be objectively measured using the Fitbit for 4 weeks.

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
Double (Investigator, Outcomes Assessor)

盲法说明

Group allocation will be concealed from study staff until the 7-day pre-intervention period begins (for preparation of corresponding e-leaflets, genetic risk estimates and/or baseline Fitbit step goal calculations), and from participants until the interventions are delivered. Given the nature of the interventions delivered, it will be impossible for participants to be blinded to the specific intervention they receive once the initial interventions are provided; however, study staff analyzing participants' de-identified data will remain blinded to participant randomization assignment.

入排标准

年龄范围
40 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • East Asian ancestry
  • Aged 40-60 years
  • Able to perform daily-living physical activity
  • Able to use English to communicate
  • Use a smartphone

排除标准

  • have been diagnosed with any type of diabetes
  • pregnant or lactating
  • unable to perform daily-life physical activities (determined through Physical Activity Readiness Questionnaire [PAR-Q])
  • participating in another research study or exercise programs
  • had experience of genetic testing
  • cannot use English

结局指标

主要结局

Changes in Fairly Active Minutes between baseline and 4-week post-intervention, and between baseline and 6-month follow-up

时间窗: Baseline, 4-week post-intervention, 6-month follow-up

Fairly Active Minutes (per day) will be objectively measured by the Fitbit tracker.

Changes in Calories Burn between baseline and 4-week post-intervention, and between baseline and 6-month follow-up

时间窗: Baseline, 4-week post-intervention, 6-month follow-up

Calories Burn (kcal per day) will be objectively measured by the Fitbit tracker.

Changes in Steps between baseline and 4-week post-intervention, and between baseline and 6-month follow-up

时间窗: Baseline, 4-week post-intervention, 6-month follow-up

Step count (per day) will be objectively measured by the Fitbit tracker.

Changes in Sedentary Minutes between baseline and 4-week post-intervention, and between baseline and 6-month follow-up

时间窗: Baseline, 4-week post-intervention, 6-month follow-up

Sedentary Minutes (per day) will be objectively measured by the Fitbit tracker.

Changes in Lightly Active Minutes between baseline and 4-week post-intervention, and between baseline and 6-month follow-up

时间窗: Baseline, 4-week post-intervention, 6-month follow-up

Lightly Active Minutes (per day) will be objectively measured by the Fitbit tracker.

Changes in Very Active Minutes between baseline and 4-week post-intervention, and between baseline and 6-month follow-up

时间窗: Baseline, 4-week post-intervention, 6-month follow-up

Very Active Minutes (per day) will be objectively measured by the Fitbit tracker.

次要结局

  • Changes in diastolic blood pressure between baseline and 6-month follow-up(Baseline and 6-month follow-up)
  • Changes in hand grip strength between baseline and 6-month follow-up(Baseline and 6-month follow-up)
  • Changes in Hemoglobin A1c (HbA1c) between baseline and 6-month follow-up(Baseline and 6-month follow-up)
  • Changes in body mass index (BMI) between baseline and 6-month follow-up(Baseline and 6-month follow-up)
  • Changes in systolic blood pressure between baseline and 6-month follow-up(Baseline and 6-month follow-up)
  • Changes in Total cholesterol between baseline and 6-month follow-up(Baseline and 6-month follow-up)
  • Changes in Self-reported Physical Activity between baseline and Immediate post-intervention, between baseline and 4-week post-intervention, and between baseline and 6-month follow-up(Baseline, Immediate post-intervention, 4-week post-intervention, 6-month follow-up)
  • Changes in Self-reported Fruit and Vegetable Consumption between baseline and Immediate post-intervention, between baseline and 4-week post-intervention, and between baseline and 6-month follow-up(Baseline, Immediate post-intervention, 4-week post-intervention, 6-month follow-up)
  • Changes in High-density lipoproteins (HDL) between baseline and 6-month follow-up(Baseline and 6-month follow-up)
  • Changes in Low-density lipoproteins (LDL) between baseline and 6-month follow-up(Baseline and 6-month follow-up)
  • Changes in Triglycerides between baseline and 6-month follow-up(Baseline and 6-month follow-up)
  • Changes in Self-reported Smoking Status between baseline and Immediate post-intervention, between baseline and 4-week post-intervention, and between baseline and 6-month follow-up(Baseline, Immediate post-intervention, 4-week post-intervention, 6-month follow-up)
  • Changes in Self-reported Psychological Status between baseline and Immediate post-intervention, between baseline and 4-week post-intervention, and between baseline and 6-month follow-up(Baseline, Immediate post-intervention, 4-week post-intervention, 6-month follow-up)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Kim, Youngwon

Assistant Professor

The University of Hong Kong

研究点 (1)

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