Augmented Reality

4

Review clinical trials related to Augmented Reality. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Augmented Reality/Virtual Reality (AR/VR) for Ultrasound-guided Medical Procedures

The study seeks to assess the efficacy of incorporating augmented reality (AR) or virtual reality (VR) technology into ultrasound-guided medical procedures such as regional anesthesia and line placement. By utilizing AR/VR devices, the investigators will improve the ergonomics when using ultrasound to guide procedures. The aims are to enhance visualization of anatomical structures and improve procedural accuracy for clinicians. The study aims to evaluate the feasibility, and effectiveness of integrating AR/VR technology into ultrasound-guided procedures, with the ultimate goal of improving patient outcomes.

Participants needed: 100
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Stanford UniversityUpdated: May 7, 2026Locations: 1
Eligibility criteria

adult patients presenting for ultrasound-guided procedures, with ASA physical st...

pregnancy [+2]

Status: Not yet recruiting

The Effect of Augmented Reality Based Training on Preeclampsia Case

However, no study has been found in the care of preeclampsia, which is highly effective on maternal and fetal health. Therefore, this study was planned to determine the effect of augmented reality-based training on the diagnosis and intervention planning skills of nursing students.

Participants needed: 84
Trial details
Age: 18-45Biological sex: FemaleType: InterventionalSponsor: Inonu UniversityUpdated: Dec 12, 2024Locations: 1
Eligibility criteria

Continuing the course of Women's Health and Diseases Nursing, [+2]

- Not watching the whole case given with virtual glasses, [+1]

Status: Recruiting

A Low-Cost Balance Training Platform Using Augmented Reality in Neurorehabilitation: a Usability Study

The goal of this clinical trial is to assess the Usability, adherence, acceptance, and security of an augmented reality platform for balance training in patients with balance disorders due to degenerative injuries or cerebrovascular diseases. The main questions it aims to answer are: * Is the augmented reality system usable, acceptable, and safe with good adherence? * Does the system improve the balance in our population? * Participants will be asked to assist at Vall d'Hebrón Hospital, where patients will undergo balance training under the supervision of a physiotherapist three days a week for four weeks. * If the patients meet the inclusion criteria, the intervention will be extended for two more weeks at home.

Participants needed: 15
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Hospital Universitari Vall d'Hebron Research InstituteUpdated: Oct 4, 2024Locations: 1
Eligibility criteria

Balance impairment due cerebrovascular diseases or neurodegenerative diseases. [+8]

The presence of a condition or abnormality that could compromise the patient's s... [+5]

Status: Not yet recruiting

Augmented Reality in Learning Anatomy: The TEACHANATOMY Randomized Cross-over Trial

Cadaver use in anatomy education is undergoing several limitations in many universities, due to high costs, time constraints and supply difficulties. As alternatives to cadaver dissections, new teaching methods based on visual technologies, such as augmented reality (AR), are being implemented worldwide. Augmented reality (AR), based on virtual interactive 3-dimensional elements (holograms) overlaid in the real-world, represents a promising alternative to explore the human body. In this study, we will test the efficacy of AR as an alternative teaching method in anatomy education by comparing traditional learning methods based on 2-dimensional (2D) images, videos, and online learning programs with the novel AR learning module The primary endpoint will consist of the score in the final theoretical and practical knowledge tests, assessed at two timepoints: immediately after the study session and after 3 months. Secondary endpoints will include adverse health symptoms and user experience, assessed immediately after the study session.

Participants needed: 300
Trial details
Age: 18-25Biological sex: AllType: InterventionalSponsor: Balgrist University HospitalUpdated: Aug 13, 2024
Eligibility criteria

Medical students attending the 1st or 2nd year of undergraduate medical educatio... [+1]

Epilepsy [+4]