跳至主要内容
临床试验/NCT05039528
NCT05039528已完成不适用

Design and Usability Testing of a Tailored Intervention to Increase Awareness About Sleep and Sleep Disorders Among Transportation Workers

Brigham and Women's Hospital1 个研究点 分布在 1 个国家目标入组 38 人开始时间: 2022年10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
入组人数
38
试验地点
1
主要终点
Change in OSA self-management efficacy as measured by the Survey of OSA Functional Health Literacy (SOFHL)

研究概览

简要总结

The objective of this protocol is to conduct a focus group to identify OSA beliefs, attitudes, and knowledge among employees in the transportation industry on shift schedules.

详细描述

Transportation shift workers (TSW, e.g., overnight, on-call, or rotating) have been identified as a high-risk group for health conditions (e.g., obesity, cardiovascular disease). Also, TSW are at risk for obstructive sleep apnea (OSA). According to one study, approximately 36% of TSWs have OSA, a condition that exacerbates health risks and daytime sleepiness. A recent report from the American Academy of Sleep Medicine (AASM) showed that those with untreated OSA cost on average $4,261 more than those without OSA. Also concerning, workers with OSA who are non-adherent to recommended OSA treatment (i.e., continuous positive airway pressure, CPAP) are at particularly high risk for motor vehicle accidents compared to those who are adherent.

This protocol outlines focus groups that will aim to identify knowledge, attitudes, and beliefs about OSA among TSW. Results of these focus groups will be used in future research to design a tailored website for relaying OSA information to TSW.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Participant)

入排标准

性别
All
接受健康志愿者
是

入选标准

  • •Age 18 years or older
  • •Access to a smartphone device
  • •Commitment to completing all study activities
  • •Score 4 or higher (mild or higher on OSA risk) according to the Apnea Risk Evaluation System (ARES) questionnaire.

排除标准

  • •Significant medical or psychiatric illness according to the PROMIS Short Form (SF-12)
  • •No OSA risk (a score below 4 on the ARES).

研究组 & 干预措施

Intervention

Experimental

Participants will receive the personalized OSA messages.

干预措施: Personalized OSA messages (Behavioral)

Control

Placebo Comparator

Placebo participants will receive no treatment during the experiment.

干预措施: Control (Other)

结局指标

主要结局

Change in OSA self-management efficacy as measured by the Survey of OSA Functional Health Literacy (SOFHL)

时间窗: The SOFHL will be administered at baseline and post-intervention. Change in SOFHL score on self-management efficacy will be computed by comparing responses at baseline and post-intervention.

OSA self-management efficacy will be examined using the SOFHL

次要结局

  • Change in Daytime sleepiness as measured by the Epworth Sleepiness Scale (ESS).(Sleepiness will be assessed at baseline and post-intervention. Change in daytime sleepiness will be computed by comparing responses at baseline and post-intervention..)
  • Change in Attentional Failures as measured by previously validated questions assessing Attentional Failures.(Attentional failures will be measured at baseline and post-intervention.Change in attentional failures will be computed by comparing responses at baseline and follow-up.)
  • Change in OSA general knowledge as measured by the SOFHL.(The SOFHL will be administered at baseline and post-intervention. Change in SOFHL score on OSA general knowledge will be computed by comparing responses at baseline and post-intervention.)

研究者

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

Rebecca Robbins

Assistant Professor of Medicine at Harvard Medical Scool and Associate Scientist at Brigham & Women's Hospital

Brigham and Women's Hospital

研究点 (1)

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