Effect of Virtual Reality Application Applied to Patients with Total Knee Replacement At Different Times
NCT ID: NCT06792123
Last Updated: 2025-01-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ACTIVE_NOT_RECRUITING
NA
120 participants
INTERVENTIONAL
2024-04-21
2025-04-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Effect of Virtual Reality on Patient Outcomes and Satisfaction in Total Knee Replacement
NCT06933732
Effect of Intraoperative Virtual Reality on Anxiety and Vital Findings in Patients Total Knee Replacement Surgery
NCT05668143
Effect of Virtual Reality-Based Relaxation Exercise on Postoperative Pain and Kinesiophobia After Total Knee Replacement
NCT06591832
Effects of Virtual Reality in TKA Patients
NCT05875324
Applicability and Efficiency of Virtual Reality Intervention in Knee Surgery Patients
NCT06311994
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
SUPPORTIVE_CARE
DOUBLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
group 1
pre-op VR application group
pre-op VR application group
VR application group during preoperative process
Group 2
Intra-op VR application group
intra-op VR application group
VR application group during intraoperative process
Control
Standart care and treatment
No interventions assigned to this group
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
pre-op VR application group
VR application group during preoperative process
intra-op VR application group
VR application group during intraoperative process
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* No psychiatric medication
* No mental and cognitive disabilities
* Those who underwent Total Knee Replacement,
Exclusion Criteria
* Receiving general anesthesia
* Experiencing complications during surgery
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Özge İşeri
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Özge İşeri
Assistant Professor, Ondokuz Mayıs University
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Özge İşeri Assistant Professor, PhD
Role: STUDY_DIRECTOR
Ondokuz Mayıs University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Ondokuz Mayıs Unıversity
Samsun, Atakum, Turkey (Türkiye)
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Ondokuz Mayıs University
Identifier Type: OTHER
Identifier Source: secondary_id
OMUKAEK 2023/423
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.