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临床试验/NCT04204486
NCT04204486Unknown早期 1 期

A Multidisciplinary Evaluation on the Effects of an Exercise Intervention on Markers of Health, Wellbeing and Performance in Law Enforcement Workers

University College, London2 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2020年1月3日最近更新:
适应症

试验速览

阶段
早期 1 期
入组人数
90
试验地点
2
主要终点
Change in upper body strength endurance (push)

研究概览

简要总结

This study aims to assess current health and fitness of law enforcement workers in various roles, and to evaluate the impact of an exercise intervention on markers on physical and mental wellbeing in this population.

The intervention will consist of an exercise programme specifically targeted at improving, physical fitness and reducing musculoskeletal pain. Participants will be randomised to three groups: a face to face intervention group, an online intervention group an a control group.

Self-reported physical health, musculoskeletal complaints, quality of sleep and occupational stress will be measured via questionnaires. Pre and post measures of fitness will be measured via functional strength testing and a cardiopulmonary exercise test. Pre and post cognitive function will be measured via computer-based cognitive tests and brain functional near-infrared spectroscopy (fNIRS). Systemic inflammation will be measured via hsCRP. Risk of typeII diabetes will be measured via HbA1c. Daily physical activity and quality of sleep will be measured via accelerometry and heart rate telemetry.

It is hypothesised that, upon completion of the programme, there will be an improvement in cardiovascular fitness and physical strength, reduced musculoskeletal pain, improved cognitive readiness and improved overall mental health and wellbeing.

详细描述

Randomisation Participants will be stratified by shift pattern and by role, and will be randomised to one of three intervention arms using permuted blocks of 3 and 6.

Self-reported information After the consent forms and PAR-Q have been signed, an Operational Police Stress Questionnaire (PSQ-Op), Impact of Events Scale (IES-R), a Leeds Sleep Evaluation (LSE) and an overall health and injury questionnaire (Nordic scale) will be sent to the officers via email using Gorilla software in December 2019.

Participants will be interviewed on the quality of their dietary intake. Trained nutrition research students will collect responses to a Food Frequency Questionnaire (FFQ) in a face to face interview.

Wearables Participants will be given wearable devices to measure their levels of physical activity during an 8-day period (full on and off shift cycle) before the intervention: the heart rate of each participant will be monitored via a Polar heart rate monitor and movement will be measured via an accelerometer worn on the non-dominant wrist (Actigraph, Pensacola, USA). Levels of physical activity, quality of sleep and heart rate variability will be processed as anonymised data on a computer. Participants will be asked to log the quality of their sleep every time they wake up from a long sleep via a Pittsburgh Sleep Quality Index (PSQI). No individuals other than the researchers will have access to the data from the wearable devices. The data will be downloaded from the device and stored in a password-protected file, on an encrypted, password-protected UCL computer in a locked cabinet. After downloading the data to the computer, the wearable device will be formatted.

Oral tests Participant oral health will be assessed on site at the respective stations in January. Oral inflammation has been shown to affect systemic health with cross-sectional evidence suggesting a negative effect on physical activity in Brazilian police. Oral health will be assessed using validated outcome measures routinely employed in both NHS dental practice and research, including: the visual assessment of inflammation of the gum edge and measurement of the depth of the gum pocket (mm) following gentle probing with a calibrated blunt probe; and tooth decay screening assessed through standard clinical methods. Together, these assessments take approximately 15 minutes.

研究设计

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

入排标准

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

入选标准

  • Working in law enforcement

排除标准

  • Participants with any form of physical injury, neuromuscular, respiratory or cardiovascular condition

结局指标

主要结局

Change in upper body strength endurance (push)

时间窗: Change from baseline after 8 weeks

Numbers of pushups performed in one minute with good form (eg. not dipping the hips and using full range of motion)

Changes in musculoskeletal pain: measured via the Nordic Scale

时间窗: Change from baseline after 8 weeks

Complaints of musculoskeletal pain, collected via a Nordic Scale. The scale runs from 0-10, where 0 is no pain at all and 10 is worst imaginable pain.

Change in leg strength, measured via the Triple Hop test

时间窗: Change from baseline after 8 weeks

Participants perform three hops on one leg. The total distance (cm) of the three hops is recorded. The test is repeated for both legs.

Change in lower limb power

时间窗: Change from baseline after 8 weeks

Participants perform a counter-movement jump on a jump mat (Chronojump). Power (Watts) is recorded.

Change in Cardiovascular fitness

时间窗: Change from baseline after 8 weeks

measured via CPET test

Change in upper body strength endurance (pull)

时间窗: Change from baseline after 8 weeks

Numbers of inverted rows performed in one minute with good form (eg. not dipping the hips and using full range of motion)

Change in hand grip strength

时间窗: Change from baseline after 8 weeks

Hand grip strength (Newtons) is measured with a hand-held dynamometer.

次要结局

  • Change in Motor Inhibition after an exercise intervention(Change from baseline after 8 weeks)
  • Change in source memory after maximal exercise(Change from baseline after a single bout of maximal exercise (CPET))
  • Change in Motor Inhibition after maximal exercise(Change from baseline after a single bout of maximal exercise (CPET))
  • Change in source memory after an exercise intervention(Change from baseline after 8 weeks)
  • Change in simple reaction time after an exercise intervention(Change from baseline after 8 weeks)
  • Changes in blood flow in the prefrontal cortex after maximal exercise(Change from baseline after a single bout of maximal exercise (CPET))
  • Changes in blood flow in the prefrontal cortex after an exercise intervention(Change from baseline after 8 weeks)
  • Change in levels of Occupational Stress(Change from baseline after 8 weeks)
  • Nutrition(Change from baseline after 8 weeks)
  • Change in simple reaction time after maximal exercise(Change from baseline after a single bout of maximal exercise (CPET))
  • Cognitive failures(Change from baseline after 8 weeks)
  • Gum inflammation (oral health)(Baseline)
  • Change in levels of Trauma(Change from baseline after 8 weeks)
  • Change in Lifestyle - Physical activity levels(Change from baseline after 8 weeks)
  • Changes in Quality of Sleep (objective)(Change from baseline after 8 weeks)
  • Changes in Quality of Sleep (subjective)(Change from baseline after 8 weeks)
  • Changes in Systemic inflammation(Change from baseline after 8 weeks)
  • Changes in Risk of type II diabetes(Change from baseline after 8 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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