← Back to Clinical Trials
Recruiting NCT07407712

NCT07407712 Better Outcomes Through Optimal Sleep in Surgical Training

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT07407712
Status Recruiting
Phase
Sponsor Sheffield Teaching Hospitals NHS Foundation Trust
Condition Staff
Study Type INTERVENTIONAL
Enrollment 20 participants
Start Date 2026-01-01
Primary Completion 2027-12-01

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Sleep intervention

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 20 participants in total. It began in 2026-01-01 with a primary completion date of 2027-12-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This research project is investigating the impact of sleep quality on cognitive and laparoscopic surgical performance. The background to this study is the growing recognition that factors beyond technical skill, such as sleep, can significantly influence a surgeon's performance. The aim is to understand how sleep patterns affect surgeons' ability to perform surgical tasks, both technically and cognitively. After this, we will aim to see if a targeted sleep intervention has a positive impact on technical skills and cognitive performance. This is a preliminary feasibility study and is part of ongoing research by the research team.

Eligibility Criteria

Inclusion Criteria: * The study will recruit general surgical trainees and consultant surgeons from the Yorkshire and Humber region. * Individuals must be willing and able to give informed consent to take part in the study. Exclusion Criteria: * • Participants with a previously diagnosed sleep disorder * Anyone who is unable to give informed consent will be excluded. * Individuals who are not general surgical trainees or consultant will be excluded. * Participants who are unable to wear the Actigraphy device continuously for two weeks, complete the daily sleep diary, or attend the in-person assessments will be excluded.

Contact & Investigator

Central Contact

Respiratory Research Coordinator

✉ sth.researchadministration@nhs.net

📞 01142265424

Frequently Asked Questions

Who can join the NCT07407712 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Staff. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07407712 currently recruiting?

Yes, NCT07407712 is actively recruiting participants. Contact the research team at sth.researchadministration@nhs.net for enrollment information.

Where is the NCT07407712 trial being conducted?

This trial is being conducted at Sheffield, United Kingdom.

Who is sponsoring the NCT07407712 clinical trial?

NCT07407712 is sponsored by Sheffield Teaching Hospitals NHS Foundation Trust. The trial plans to enroll 20 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology