the effect of computer generated virtual reality in patients undergoing palliative pain interventions
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/064507
- Lead Sponsor
- Banaras Hindu University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Chronic cancer patients undergoing pain intervention between 18 to 70 years having NRS more than 4
Exclusion Criteria
1.Patients with sepsis
2.Patients with local site infections
3.Patients with allergy to local anesthetics
4.Patients with coagulation abnormalities
5.Mentally unstable patients
6.Patients with hemodynamic instability
7.Patients with visual and hearing defects
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the perceived pain as assessed by Numerical Rating Scale (NRS) between the study and control group and <br/ ><br>Timepoint: To compare the pain using Numerical Rating Scale (NRS) between the study and control group at baseline 15 minutes before the procedure and after the procedure at 0 hours <br/ ><br>
- Secondary Outcome Measures
Name Time Method 1)To compare the change in distress as assessed by Distress Inventory for Cancer between the two groups (DIC-2) <br/ ><br>2)To compare the Edmonton Symptom Assessment System-revised score between the two groups (ESAS-r) <br/ ><br>3)To compare the post-procedure NRS score at 0, 6, 12, and 24 hours between the two groups <br/ ><br>4) To compare the Post-procedure analgesic requirements between the two groups up to 24 hours <br/ ><br>5)To compare the Patient satisfaction score as per Likerts’ scale between the two groupsTimepoint: DIC-2, NRS, Patient satisfaction score will be assessed at 0 hours, 6 hours, 12 hours and 24 hours