An observational study in Anesthesia Residents and Critical Care Staff, sponsored by Ain Shams University. Not yet recruiting. Per ClinicalTrials.gov, last updated 2026-10-16.
Sponsored by Ain Shams University · Observational
This survey aims to find the relation, if any, between the perceived work load and the adopted coping strategy among newly recruited anesthesia and critical care residents.
This survey assesses the work load perceived by newly recruited anesthesia and critical care residents as evaluated with the National Aeronautics and Space Administration Task Load Index (NASA-TLX) and relate it to the type of coping strategy adopted by them as assessed using the Coping Inventory for Stressful Situations (CISS).
Ain Shams University is the lead sponsor of 1,930 studies on the registry; 433 are open to participants now.
Of its 33 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.
Counted across the registry records on this site, refreshed daily.
Anesthesia and critical care residents of either sex who have spent 3 to 6 months of their training program working in operating theaters, intensive care units, or pain management units.
Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.
Exclusion Criteria:
Anesthesia and critical care residents who have started their residency program for 3 to 6 month.
Other: NASA-TLX to assess the perceived work load
This inventory assesses the coping strategy
Also known as: CISS
Coping Inventory for Stressful Situations (CISS) Questionnaire
The Coping Inventory for Stressful Situations (CISS) is a standardized questionnaire assessing three main coping styles: Task-Oriented, Emotion-Oriented, and Avoidance-Oriented coping. The CISS questionnaire consists of 48 items, with responses rated on a 5-point Likert scale ranging from 1 (Not at all) to 5 (Very much).
Time frame: After spending 3 to 6 months in the residency program.
No study locations are listed for this record.
Plan to share: Yes — Data will be available from the study director (S.M.H.) upon reasonable request.
No publications or documents are linked to this record.
Start is estimated for Nov 2026; primary completion for May 2027, 6 months later.
How these figures are worked out, and which studies are left out of them.
From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗
This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.
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