Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT07407712

Better Outcomes Through Optimal Sleep in Surgical Training

Led by Sheffield Teaching Hospitals NHS Foundation Trust · Updated on 2026-02-12

20

Participants Needed

1

Research Sites

99 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Better Outcomes Through Optimal Sleep in Surgical Training

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • General surgical trainees and consultant surgeons from the Yorkshire and Humber region
  • Willing and able to give informed consent to take part in the study
Not Eligible

You will not qualify if you...

  • Participants with a previously diagnosed sleep disorder
  • Anyone unable to give informed consent
  • Individuals who are not general surgical trainees or consultant surgeons
  • Participants unable to wear the Actigraphy device continuously for two weeks
  • Participants unable to complete the daily sleep diary or attend in-person assessments

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Sheffield Teaching Hospitals

Sheffield, United Kingdom

Actively Recruiting

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Research Team

R

Respiratory Research Coordinator

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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