Anxiety / Surgical Fear Scale / Experimental Group · Interventional Study
ClinicalTrials.gov · August 19, 2026
Early or partial results. Treat as a signal, not a conclusion.
This is a completed clinical trial registration for a single-arm or inadequately specified comparative study of immersive VR on preoperative anxiety in bariatric surgery patients. No results are posted in this registry record; the study cannot be evaluated for efficacy, and the evidence base remains absent.
Interventional, Randomized, Parallel, Single masking, Prevention purpose. Virtual Reality, Surgical Fear Scale, Anxiety; age from 20 Years; to 60 Years. Intervention: VR group. Compared with: Control group — No Intervention. n = 120. 1 site: Turkey (Türkiye).
This is a completed clinical trial registration for a single-arm or inadequately specified comparative study of immersive VR on preoperative anxiety in bariatric surgery patients. No results are posted in this registry record; the study cannot be evaluated for efficacy, and the evidence base remains absent.
Safety was not reported in the material analysed. Check the source before drawing any conclusion about harm.
The source did not state who this applies to in practice.
This is a completed registry record with no posted results; the study design and enrollment are documented but outcomes remain unreported, precluding evidence evaluation.
As stated by the source record.
Quoted from the source exactly as published.
Graded across the dimensions that decide whether you should act, each from what the source actually supports. There is no single score, and where a dimension was not assessed it says so.
What is missing. This record has no key findings. That is a gap in the analysis, not a judgement about the study.
Registry record from ClinicalTrials.gov (NCT07774156). This is a study registration, not published results. Lead sponsor: Firat University. Recruitment status: COMPLETED. Phase: NA. Study type: INTERVENTIONAL. Enrollment: 120 participants (ACTUAL). Conditions: Virtual Reality, Surgical Fear Scale, Anxiety. Interventions: BEHAVIORAL: Experimental Group. Primary outcome measures: Surgical Fear Questionnaire (SFQ) , 40 minutes. Brief summary: To determine whether a single 20-minute immersive VR nature session delivered in the immediate preoperative period reduces surgical fear and state anxiety in patients scheduled for bariatric surgery.
Taken from the source record, never inferred. Follow any of these and new work involving them reaches your briefing.