[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100624290":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":20,"centralContacts":21,"locations":27,"responsibleParty":43,"collaborators":20,"id":45,"slug":46,"hasResults":47,"nctId":48,"briefTitle":49,"officialTitle":49,"acronym":50,"eligibilityCriteria":51,"healthyVolunteers":52,"sex":53,"minAge":54,"maxAge":20,"enrollmentInfo":55,"targetDuration":20,"studyType":58,"phases":59,"briefSummary":61,"conditions":62,"keywords":20,"overallStatus":30,"whyStopped":20,"lastUpdateSubmitDate":64,"lastUpdatePostDateStruct":65,"startDateStruct":68,"completionDateStruct":70,"leadSponsor":72,"locationsCount":73},{"fullName":5,"class":6},"Sheffield Teaching Hospitals NHS Foundation Trust","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"All participants","EXPERIMENTAL","All participants will have a sleep intervention",[13],"Behavioral: Sleep intervention",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"BEHAVIORAL","Sleep intervention","Participants will have a face-to-face consultation with a sleep consultant, which will be tailored to the specific sleep profile.\n\n* The consultation will include advice on sleep hygiene and may involve identifying potential sleep disorders.\n* They may be referred for additional testing at a local sleep lab if a sleep disorder is suspected.\n* 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.",[9],null,[22],{"name":23,"role":24,"phone":25,"phoneExt":20,"email":26},"Respiratory Research Coordinator","CONTACT","01142265424","sth.researchadministration@nhs.net",[28],{"facility":29,"status":30,"city":31,"state":20,"zip":20,"country":32,"countryCode":33,"cosmosGeoPoint":34,"geoPoint":39,"contacts":40},"Sheffield Teaching Hospitals","RECRUITING","Sheffield","United Kingdom","UK",{"type":35,"coordinates":36},"Point",[37,38],-1.4659,53.38297,{"lat":38,"lon":37},[41],{"name":42,"role":24,"phone":25,"phoneExt":20,"email":26},"Respiratory research coordinator",{"type":44,"investigatorFullName":20,"investigatorTitle":20,"investigatorAffiliation":20,"oldNameTitle":20,"oldOrganization":20},"SPONSOR","100624290","better-outcomes-through-optimal-sleep-in-surgical-training-100624290",false,"NCT07407712","Better Outcomes Through Optimal Sleep in Surgical Training","BOOST","Inclusion Criteria:\n\n* The study will recruit general surgical trainees and consultant surgeons from the Yorkshire and Humber region.\n* Individuals must be willing and able to give informed consent to take part in the study.\n\nExclusion Criteria:\n\n* • Participants with a previously diagnosed sleep disorder\n\n  * Anyone who is unable to give informed consent will be excluded.\n  * Individuals who are not general surgical trainees or consultant will be excluded.\n  * 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.",true,"ALL","18 Years",{"count":56,"type":57},20,"ESTIMATED","INTERVENTIONAL",[60],"NA","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.",[63],"Staff","2026-02-05",{"date":66,"type":67},"2026-02-12","ACTUAL",{"date":69,"type":67},"2026-01-01",{"date":71,"type":57},"2027-12-01",{"name":5,"class":6},1]