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Pelvic vs Virtual Reality Simulator

Cairo University (CU) logo

Cairo University (CU)

Status

Completed

Conditions

Laparoscopic Training

Treatments

Device: Pelvic trainer:
Device: Virtual reality Simulator

Study type

Interventional

Funder types

Other

Identifiers

NCT05255614
Pelvic trainer vs VRS

Details and patient eligibility

About

The aim of this study is to evaluate the proper sequence of Pelvic trainer and VR simulator training in order to improve gynecological laparoscopic skills and assess training levels.

Full description

In this study, the investigators will determine the proper sequence of simulation training. Pelvic Trainer Versus Virtual reality Simulator in order to improve laparoscopic skills of residents with no or little previous laparoscopic experience.

  • This study will compare the proper sequence of simulation training. Pelvic Trainer Versus Virtual reality Simulator of two groups: Group A versus Group B.
  • Group A will start training on the pelvic trainer (training on educational intervention 1) and assessment will be via assessment via a checklist (test 1). Then at a later time, they will be trained on VR simulator (Sim Surgery) (educational intervention 2) and assessment will be via Electronic auto assessment via the Simulator (test 2).
  • Group B will start training on the VR simulator (Sim Surgery) (educational intervention 2) and assessment will be via Electronic auto assessment via the Simulator (test 2). Then at a later time, they will be trained on the pelvic trainer (training on educational intervention 1) and assessment will be via assessment via a checklist (test 1).

Enrollment

20 patients

Sex

All

Ages

26 to 29 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All the residents in Obstetrics and Gynecology department who have no or little previous laparoscopic experience

Exclusion criteria

  • Residents who have previous good laparoscopic experiences.
  • Age below 26 or Above 29 years

Trial design

Primary purpose

Health Services Research

Allocation

Non-Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

20 participants in 2 patient groups

First Group
Active Comparator group
Description:
the participants will start training on the pelvic trainer and assessment will be via assessment via a checklist. Then at a later time, they will be trained on VR simulator (Sim Surgery) and assessment will be via Electronic auto assessment via the Simulator.
Treatment:
Device: Pelvic trainer:
Device: Virtual reality Simulator
Second Group
Active Comparator group
Description:
the participants will start training on VR simulator (Sim Surgery) and assessment will be via Electronic auto assessment via the Simulator. Then at a later time, they will be trained on the pelvic trainer and assessment will be via assessment via a checklist.
Treatment:
Device: Pelvic trainer:
Device: Virtual reality Simulator

Trial contacts and locations

1

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Central trial contact

Marwa M Abdalla, MD

Data sourced from clinicaltrials.gov

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