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临床试验/NCT05250700
NCT05250700Unknown不适用

Characterisation of Objectively Measured Physical Activity and Self-reported Habitual Exercise in Healthy Adults. An Observational Trial

University of Bath1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2020年11月4日最近更新:
适应症

试验速览

阶段
不适用
入组人数
66
试验地点
1
主要终点
Total energy expenditure [kilocalories per minute]

研究概览

简要总结

This study aims to observe participants' physical activity (PA) using a blinded multisensor physical activity monitor as they go about their typical daily physical activities across a 6-week time frame. Participants will also complete a subjective, self-reported, online form to denote structured activities undertaken.

详细描述

This study will observe participants' objectively measured PA and energy expenditure in a naturalistic manner. Individuals expressing interest will be invited to attend an online familiarisation meeting to assess eligibility for the study - procedures will be presented/explained in detail before participants are given a chance to question and discuss any concerns. Once aware of the requirements, participants will be asked if they wish to take part in the main trial and asked for written informed consent.

In Visit 1 (Day 0) willing participants will then undergo a familiarisation of protocol components, and they will be provided with the SenseWear armband to be worn, constantly, over a 42-day period (except during water-based activities such as showering and swimming). The device does not include a display and so participants are blinded to the measurement. Participants will be instructed to continue with their normal lifestyles and not make any changes. On or around day 43, participants will be asked to return the device (Visit 2).

During visit 1 and visit 2 participants will be measured and weighed using a stadiometer and floor scale. Throughout the trial, weekly reminder emails will be distributed by the research team to all participants reminding them of the study requirements and providing them with an additional opportunity to raise concerns. Due to the data storage capacity of the devices, new monitors will be distributed and used monitors returned remotely via post at weeks 2 and 4.

Additionally, during this period of objective PA measurement, participants will be invited to note the start and end time of any 'structured exercise' - defined as any PA that is "planned, structured, repetitive and aimed at improving or maintaining physical fitness (Caspersen, Powell and Christenson 1985 cited by Simmich, Deacon and Russell 2019)". Participants will also be required to note time spent sleeping. Data from this self-report component of the trial will be used to demarcate bouts of purposeful, structured exercise as well as total self-reported waking time.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
40 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy adults aged 40-
  • Available to attend Department for Health, University of Bath, Bath, UK.
  • Capable of conducting typical daily task (e.g., housework, walking etc.).
  • Willingness to wear a PA monitor for 24hr for a total of 42 days.

排除标准

  • No cold/flu-like symptoms within the last month.
  • Known history of cardiac or circulatory dysfunction.
  • Known to live with diabetes or other metabolic disorders.
  • Known to live with severe visual or audio impairment.
  • Known to live with epilepsy or have seizures.
  • Known disabilities that impede daily physical activity.
  • Known allergy to nickel.

结局指标

主要结局

Total energy expenditure [kilocalories per minute]

时间窗: 6 weeks

24-hour energy expenditure will be assessed via a wearable device enabling the estimation of total daily kilocalorie expenditure.

Domain specific energy expenditure [kilocalories per minute].

时间窗: 6 weeks

24-hour energy expenditure will be assessed via a wearable device enabling the estimation of kilocalorie expenditure during sedentary (\<1.5 metabolic equivalents) , light (1.5 - 3 metabolic equivalents), moderate (3-6 metabolic equivalents), vigorous (\>6 metabolic equivalents) activities.

次要结局

未报告次要终点

研究者

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

Liam Beasley

Principal Investigator

University of Bath

研究点 (1)

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