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The effect of virtual reality on pain and anxiety during treatments for chronic lower back pain

Impact of virtual reality on procedural pain and anxiety in chronic low back pain patients: a quasi-experimental study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN11994372
Enrollment
30
Registered
2024-05-21
Start date
2022-04-16
Completion date
Unknown
Last updated
2024-06-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic low back pain Musculoskeletal Diseases

Interventions

This quasi-experimental study design will be conducted at the Intervention Unit of King Fahad University Hospital in Khobar, Saudi Arabia. Between May 2022 and May 2023, chronic low back pain (CLBP) p
odd numbers were set for the VR group and even numbers for the SD group. The nurse then prepared both groups of patients accordingly. Patients in the SD group will be given sedative medication (2-3 mg

Sponsors

Imam Abdulrahman Bin Faisal University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Both males and females were included in the study 2. Patients who had been referred to the pain clinic because they had been suffering from non-specific low back pain persisting for more than three months 3. Patients older than 18 years old 4. American Society of Anesthesiologists (ASA) physical status classification I-III The ASA physical status classification system is a pre-operative tool that helps anticipate a patient's risks. On a scale of I to VI: I represents healthy patients with minimal risks and VI represents patients who are brain dead and whose organs tend to be donated upon approval.

Exclusion criteria

Exclusion criteria: 1. Patients aged 17 years old and under 2. Patients who have visual or hearing impairments, dementia, and/or have been diagnosed with epilepsy or balance disorders.

Design outcomes

Primary

MeasureTime frame
1. Periprocedural pain intensity score measured using the numeric pain scale (with 0 denoting no pain and 10 denoting worst possible pain) before and after the procedure 2. Anxiety measured using the State-Trait Anxiety Inventory (STAI) scale before and after the procedure

Secondary

MeasureTime frame
The secondary outcome measures included: 1. Patient comfort measured using a five-point Gloucester Comfort scale, with 1 being the most comfortable and 5 being the most uncomfortable, immediately after the procedure 2. Patient satisfaction measured using a 5-point Likert scale (1 referred to dissatisfied; 2 to less satisfied; 3 to satisfied; 4 for very satisfied; and 5 for completely satisfied) once fully alert patients reach the recovery room after the procedure 3. Hemodynamic parameters: systolic blood pressure (SBP), diastolic blood pressure (DBP), heart rate (HR), and oxygen saturation (SPO2), measured using by GE Aisys CS2® anesthesia machine throughout the procedure

Countries

Saudi Arabia

Contacts

Public ContactAbrar;Abrar Bakhurji;Bakhurji

;

gs.vd@iau.edu.sa;abrar_bakhurji@hotmail.com+966538026888;+966538026888

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026