Assessing Construction Execution Under Sleep Impairment (NCT07431970) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Assessing Construction Execution Under Sleep Impairment
United States12 participantsStarted 2026-03-01
Plain-language summary
The goal of this study is to learn whether virtual reality (VR) construction tasks can detect performance changes associated with prior sleep, and to determine the extent to which these changes can be distinguished from interacting repetitively with VR itself.
Who can participate
Age range
21 Years – 49 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Fluent in English
* Tolerate virtual reality system
Exclusion Criteria:
* Recent shiftwork
* Recent travel across time zones (\>2 in last month)
* Underlying health conditions (high blood pressure, diabetes, cancer, heart attack, heart failure, angioplasty, heart surgery, etc.)
* Use of nicotine products such as tobacco or e-cigarettes
* Use of illicit drugs in the past year
* Pregnancy
* Sleep disorders (obstructive sleep apnea)
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Feasibility: Recruitment
Timeframe: From first date of recruitment activities to last day of study activities, up to 100 weeks.
2
Feasibility: Retention
Timeframe: From start of recruitment activities to the end of study activities, up to 100 weeks.
3
Feasibility: Tolerability of Repeated VR use and Physiologic Monitoring
Timeframe: Assessed each 8-hour in laboratory visit
4
Feasibility: Data Completeness and Quality
Timeframe: Through study completion, an average of 1 year