Patient undergoing lumbar puncture.
Conditions
Interventions
Intervention 1: Intervention group(A): This group receives the core study intervention. Their experince is defined by the use of Virtual Reality (VR) in addition to the standard care protocol for lumb
Sponsors
University of Baghdad/ Colloge of Nursing
University of Baghdad/ Colloge of Nursing
Unversity of Baghdad/ Colloge of Nursing
The University of Baghdad/ Colloge of Nursing
Eligibility
Sex/Gender
All
Age
18 Years to 65 Years
Inclusion criteria
Inclusion criteria: Patients undergoing for Lumbar puncture Patients suspected with Meningitis disease Patients free from chroinc health problem Agree to particpate in the study
Exclusion criteria
Exclusion criteria: Patients having cerebal spinal fluid (CSF) drainage Vitally unstable and unconscious patient Cognitive Impairment: patient unable to provide informal conset Age under 18 years old
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Primary outcome:pain intensity. Timepoint: Immediatly after procedure is complete. Method of measurement: Measured using a validate self report pain sacle Visual Analoge Sacle (VAS).;Fear and Anxiety level. Timepoint: Will be taken both before and immediatly after procedure is complete. Method of measurement: Measured using a validate self report scale Visual Analoge Scale for fear and anxiety. | — |
Secondary
| Measure | Time frame |
|---|---|
| Patient satisfaction. Timepoint: After procedure is compelet. Method of measurement: Patients asked to rate their level of satisfaction on a Visual Analoge Sacle. This sacle is a ruler 10 cm(100mm) the result is determind by measuring the distance in millimeters on vertical line ranging between. 0= not satisfied at all, 100= Iam very satisfied. The participants will give the result of satisfaction immediatly after procedure is complete. | — |
Countries
Iraq
Contacts
Public ContactAmer Maki Kasim
The University of Baghdad/ Colloge of Nursing
Outcome results
None listed