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Can mobile application-augmented reality improve better skills and knowledge in interventional pain management of lumbar facet joint with fluoroscopic guidance? Comparison with traditional method

Comparison of learning methods: mobile application-augmented reality with traditional learning for interventional pain management skills of lumbar facet joint with fluoroscopic guidance

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN17740832
Enrollment
82
Registered
2024-01-30
Start date
2024-02-05
Completion date
Unknown
Last updated
2024-05-21

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

Conditions

Residents of anesthesiology and intensive care department Not Applicable

Interventions

Current interventions as of 07/05/2024: The study will use a single-blind randomization controlled trial design to investigate the improvement of skill and knowledge of anesthesiology and intensive

Sponsors

Universitas Gadjah Mada
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Current inclusion criteria as of 07/05/2024: 1. Resident of anesthesiology and intensive care department that had passed pain module 2. Willing to take part in research by signing informed consent _____ Previous inclusion criteria: 1. Resident of anesthesia that had passed pain module 2. Willing to take part in research by signing informed consent

Exclusion criteria

Exclusion criteria: 1. Has previously done intervention for lumbar facet joint pain using fluoroscopic guidance 2. Can't speak Indonesian

Design outcomes

Primary

MeasureTime frame
Skills measured using Objective Structured Clinical Examination (OSCE), participants will be examined by given cases and asked to do a simulation of pain intervention or management. The examiner will have a checklist for OSCE scoring (the checklist was made by the investigator and validated by the anesthesiologist and pain management expert). Participants will be given 20 minutes for each case/station.

Secondary

MeasureTime frame
Knowledge measured using questions formulated by the investigators and validated by an anesthesiologist or pain management specialist/expert. The pre-test will be done before all participants are exposed to the learning method (lecture or application). The post-test will be given after all participants finish all the courses.

Countries

Indonesia

Contacts

Public ContactMahmud Mahmud
mahmudanestesi@ugm.ac.id+62-8122697997

Outcome results

None listed

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