The Effect of Preoperative Training With Virtual Reality on Anxiety, Readiness for Surgery and Recovery Process of Patients in Colorectal Cancer Surgery
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In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Patients undergoing colorectal surgery will be trained using virtual reality glasses..
- Who it may be relevant to
- Registry conditions: Anxiety, Surgical Preparation, and Recovery Process in Colorectal Cancer Surgery. Basic parameters: 18 years — 70 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Turkey (Türkiye)
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
The aim of the study is to determine the effect of The Effect of Preoperative Training with Virtual Reality on Anxiety, Readiness for Surgery and Recovery Process of Patients in Colorectal Cancer Surgery. Research Hypotheses In patients undergoing colorectal surgery: H1 The comfort level of patients who received preoperative training using virtual reality is higher than that of patients who received training using written brochures and the control group. H2. The anxiety level of patients who received preoperative education using the virtual reality method is lower than that of patients who received education via written brochures and the control group. H3 The satisfaction level of patients who received preoperative education using the virtual reality method is lower than that of patients who received education via written brochures and the control group.
Interventions
- Device Patients undergoing colorectal surgery will be trained using virtual reality glasses.
Patients undergoing colorectal surgery will be trained using virtual reality glasses.
Primary outcome measures
- (State Trait Anxiety Inventory I-II) [Time frame: 24 hour]
- The Preparedness for Colorectal Cancer Surgery Questionnaire (PCSQ) [Time frame: 24 hour]
- Recovery Quality-40 Survey (QoR-40) [Time frame: 24 hour]
Secondary outcome measures (2)
- Cortisol Level [Time frame: 24 hour]
- Number of Steps [Time frame: 24 hour]
Eligibility criteria
Inclusion criteria
Agreement to participate in the study, Ability to read and write in Turkish, Being conscious and communicative.
Exclusion criteria
Those with any psychiatric illness, Those diagnosed with an anxiety disorder and taking medication for anxiety, Those with active nausea, vomiting, or headache, Those with vision or hearing problems, Those with a history of seizures
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Single blind
- Primary purpose
- Supportive care
Study locations
Turkey (Türkiye) · 1 center
- İstanbul University-Cerrahpasa — Istanbul
Identifiers
NCT: NCT07294690 · E-83045809-604.01-1017096