- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT03453736
Staff Experiences in Robotic Theatres
A Qualitative Study of Staff Experiences and Practices Within the Robotic Theatre Setup
Studies have shown that team work impacts patients safety. This is particularly the case in surgical theatres where individuals from different backgrounds (surgeon, anaesthetists, nurses, ..etc) work together to achieve a common goal which is looking after the patient. The robotic theatre set up is different due to the physical separation of the surgeon from the patient and the rest of the team. This may represent a communication challenge. The Study investigators aim to study theatre staff experiences and practices of communication and teamwork in this special setup, investigating any challenges participants may be facing and possible ways of adapting to them. Staff opinions and suggestions for improvement will be explored for utmost surgical performance and patient safety.
The study will involve two parts:1) individual staff interviews and 2) teamwork observations during real life surgery. The two parts should complement each other giving an overall picture of the teamwork in the robotic theatre setup.
Studieoversikt
Studietype
Registrering (Faktiske)
Kontakter og plasseringer
Studiesteder
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-
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Leicester, Storbritannia
- University Hospitals of Leicester NHS Trust
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
Inclusion Criteria:
- Robotic theatre staff as above.
- Willing and able to participate.
- Good command of the English language.
Exclusion Criteria:
- Theatre staff not involved in robotic surgery.
- Participants not willing / unable to participate.
- Staff that have not worked in a conventional theatre setup before.
- Inability to read/speak/understand English.
- Lack of capacity for consent.
Studieplan
Hvordan er studiet utformet?
Designdetaljer
Kohorter og intervensjoner
Gruppe / Kohort |
Intervensjon / Behandling |
---|---|
Robotic procedures
Experiences and practices in Robotic theatres will be studied via semi-structured interviews with staff as well as team observations during real time robotic surgery.
As the study is a qualitative one, data collection will continue till we reach saturation of theoretical categories.
We expect 20 interviews and 10 observations to suffice.
|
This is a qualitative study involving staff interviews and observations.
No intervention is being applied.
|
Non-Robotic procedures
Staff involved in robotic surgery will have almost definitely worked in non-robotic theatres ie major abdominal and laparoscopic. Staff interviews will explore differences in experiences and practices between these different theatre setups. In addition, we aim to observe further 5 non-robotic procedures to evaluate staff teamwork and communication within the more regular theatre setup. |
This is a qualitative study involving staff interviews and observations.
No intervention is being applied.
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Robotic staff experiences.
Tidsramme: 1 year
|
This will be explored using individual interviews and team observations.
Textual data of interview transcripts and observation field notes will be analysed using constant comparative method.
|
1 year
|
Robotic staff practices
Tidsramme: 1 year
|
This will be explored using individual interviews and team observations.
Textual data of interview transcripts and observation field notes will be analysed using constant comparative method.
|
1 year
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Staff communication in robotic theatres.
Tidsramme: 1 year
|
This will be explored using individual interviews and team observations.
Textual data of interview transcripts and observation field notes will be analysed using constant comparative method.
|
1 year
|
Staff teamwork
Tidsramme: 1 year
|
This will be explored using individual interviews and team observations.
Textual data of interview transcripts and observation field notes will be analysed using constant comparative method.
|
1 year
|
Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Faktiske)
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Andre studie-ID-numre
- 0647
- 237227 (Annen identifikator: Integrated Research Application System (IRAS))
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
Legemiddel- og utstyrsinformasjon, studiedokumenter
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Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
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