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RecruitingNCT07407712BOOSTUpdated Feb 12, 2026

Better Outcomes Through Optimal Sleep in Surgical Training

An interventional study of Sleep intervention in Staff, sponsored by Sheffield Teaching Hospitals NHS Foundation Trust. Recruiting at 1 site in United Kingdom. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-02-12.

Sponsored by Sheffield Teaching Hospitals NHS Foundation Trust · Not applicable, Interventional, and Other

From the registry’s dates

  • Started Jan 2026; still recruiting 9 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
20
Allocation
Not applicable
Ages
18 Years and older
Sex
All
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Study 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.

02

Conditions studied

  • Staff
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In context

Lead sponsor

Sheffield Teaching Hospitals NHS Foundation Trust is the lead sponsor of 207 studies on the registry; 26 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

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

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.
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Study design

Phase
Not applicable
Primary purpose
Other
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
20 participants (estimated)

Study arms

  • Experimental
    All participants

    All participants will have a sleep intervention

    Behavioral: Sleep intervention

Interventions

  • BehavioralSleep intervention

    Participants will have a face-to-face consultation with a sleep consultant, which will be tailored to the specific sleep profile. * The consultation will include advice on sleep hygiene and may involve identifying potential sleep disorders. * They may be referred for additional testing at a local sleep lab if a sleep disorder is suspected. * If indicated by the sleep profile, they may receive short-form cognitive behavioural therapy for insomnia (CBTi), which typically involves a series of structured sessions.

06

What researchers measure

Primary outcomes

  1. Change in objective sleep quality as measured by Actigraphy data

    Total sleep time

    Time frame: From baseline to 8 weeks

  2. Change in objective sleep quality as measured by Actigraphy data

    sleep efficiency

    Time frame: From baseline to 8 weeks

Secondary outcomes

  1. Change in subjective sleep quality

    PSQI

    Time frame: From baseline to 8 weeks

  2. Change in subjective cognitive load

    SurgTLX

    Time frame: From baseline to 8 weeks

  3. Change in objective cognitive load

    HRV

    Time frame: From baseline to 8 weeks

  4. Change in technical surgical performance

    GOALS framework

    Time frame: From baseline to 8 weeks

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Study locations

1 of 1 sites recruiting
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References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 12, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT07407712
Lead sponsor
Sheffield Teaching Hospitals NHS Foundation Trust
Responsible party
Sponsor
First posted
Feb 12, 2026
Start date
Jan 1, 2026
Primary completion
Dec 1, 2027 (estimated)
Completion
Dec 1, 2027 (estimated)
Last update
Feb 12, 2026

Study contacts

Respiratory Research Coordinator
Contact
sth.researchadministration@nhs.net
01142265424

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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