Tianjin Medical University General Hospital
Tianjin, 300052, China
NCT Number: NCT05926817
Immersive virtual reality (VR) as a non-pharmaceutical technology may deliver effective behavioral therapies for postsurgical patients with acute pain. To determine the analgesic effects of VR on patients after thoracoscopic surgery. The investigators conducted a randomized clinical trial to determine the postoperative effect of VR on pain relief in patients undergoing thoracoscopic surgery.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
Tianjin, 300052, China
Immersive virtual reality (VR) as a non-pharmaceutical technology may deliver effective behavioral therapies for postsurgical patients with acute pain. Patients in the QTC-VR group had to participate in 15-minute interactive games wearing 3D-VR headsets. QTC-VR intervention had functions for breath-relaxation and attention-concentration training. It instructed the patients to breathe deeply with the marine animal's swimming relaxation rhythm and to constantly switch the vision field by rotating their heads and necks to catch animals. Therefore, the investigators conducted a randomized clinical trial to determine the postoperative effect of QTC-VR on pain relief in patients undergoing thoracoscopic surgery.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients in the Placebo-VR group watched a 10-minute relaxation-based 2D film through VR headsets along with receiving conventional analgesia.
Patients in the QTC-VR group engaged in 10-minute interactive pain relief 3D VR programs while wearing VR headsets along with receiving conventional analgesia.
Time frame: Evaluating pain intensity among postoperative patients 10 minutes prior to and 30 minutes following the intervention
The primary outcome was the change in pain intensity following the QTC-VR and Placebo-VR intervention.
Time frame: The patients' pain interference was evaluated within 30 minutes of the intervention.
Secondary outcomes included the pain interference on their mood.
Time frame: The patients' pain interference was evaluated within 30 minutes of the intervention.
Secondary outcomes included the pain interference on their sleep.
Time frame: The patients' pain interference was evaluated within 30 minutes of the intervention.
Secondary outcomes included the pain interference on their daily life.
Time frame: The patients' pain interference was evaluated within 30 minutes of the intervention.
Secondary outcomes included the pain interference on their enjoyment of life.
Time frame: The patients' pain interference was evaluated within 30 minutes of the intervention.
Secondary outcomes included the pain interference on their walking ability.
Time frame: We assessed patient satisfaction with VR after the end of the third day of the VR intervention.
Secondary outcomes included patient satisfaction regarding the VR intervention.
Tianjin Medical University
Other
Effect of Virtual Reality Intervention on Hospitalized Patients With Acute Pain After Thoracoscopic Surgery: A Randomized Clinical Trial
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