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The Effect of Virtual Reality Headsets on Pain, Anxiety, Patient Satisfaction, and Physiological Parameters in Patients Undergoing Open-Heart Surgery

31 oktober 2026 uppdaterad av: Gizem Göktuna, Dokuz Eylul University

The Effect of Virtual Reality Headsets on Pain, Anxiety, Patient Satisfaction, and Physiological Parameters in Patients Undergoing Open-Heart Surgery: A Randomized Controlled Trial

This randomized controlled trial aims to investigate the effects of virtual reality headset use on pain, anxiety, patient satisfaction, and physiological parameters in patients undergoing open-heart surgery. Participants will be randomly assigned to two groups: the virtual reality group and the control group. Pain levels, anxiety levels, satisfaction levels, and physiological parameters will be assessed both before and after the procedure. The study aims to determine whether this non-pharmacological method improves postoperative pain, anxiety, patient satisfaction, and physiological parameters.

Studieöversikt

Studietyp

Interventionell

Inskrivning (Beräknad)

44

Fas

  • Inte tillämpbar

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studieorter

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

Inclusion Criteria:

  • Aged 18 and older
  • Who have not previously undergone open-heart surgery
  • Non-emergency, elective surgeries
  • Who have not taken pain medication 4-6 hours prior to the procedure
  • Who have a numerical pain scale score of 3 or higher prior to the procedure
  • Patients with sufficient cognitive ability to tolerate the virtual reality headset application
  • Patients who voluntarily agree to participate in the study
  • Patients extubated on the second postoperative day
  • Patients with no history of chronic pain (e.g., arthritis)
  • Being alert and oriented enough to communicate (Glasgow Coma Scale 15)
  • Not being addicted to alcohol or drugs
  • Not using anxiolytics
  • Having no psychological problems (such as depression or anxiety disorders)
  • Being able to read and understand Turkish

Exclusion Criteria:

  • • Under 18 years of age

    • With vision or hearing loss
    • Clinically unstable
    • With a known history of epilepsy, vertigo, or limited mobility
    • With a surgical incision or scar on the face that prevents wearing VR goggles
    • Chronic opioid use or use of psychiatric medications

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Stödjande vård
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Enda

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: Virtual Reality Group

For patients admitted to the ward for surgery, the researcher will have them complete the State Anxiety Scale and the Satisfaction Scale one day before surgery. On the third postoperative day in the clinic, the researcher will fit patients with virtual reality goggles, and the patient will watch nature-themed videos-such as forest scenes, beach walks, and parks-for 10 minutes. After 10 minutes, the virtual reality session will end. Immediately after the intervention and 30 minutes later, the same researcher will have the patients complete the Numerical Pain Scale, the State Anxiety Scale, the Numerical Satisfaction Scale, and the Physiological Parameters Monitoring Form.

One day before surgery, the researcher will have participants in this group complete the State Anxiety Scale and the Satisfaction Scale. On the third postoperative day at the clinic, the researcher will fit patients with virtual reality goggles, and the patient will watch nature-themed videos-such as forest scenes, beach walks, and parks-for 10 minutes. After 10 minutes, the virtual reality session will end. Immediately after the intervention and 30 minutes later, the same researcher will have the patients complete the Numerical Pain Scale, the State Anxiety Scale, the Numerical Satisfaction Scale, and the Physiological Parameters Monitoring Form. This distraction technique aims to reduce pain perception and anxiety levels, increase patient satisfaction during the procedure, and improve physiological parameters.

Andra namn:
  • VR-glasögon
Inget ingripande: Control Group

Patients admitted to the ward for surgery will complete the State Anxiety Scale and the Satisfaction Scale administered by the researcher one day before surgery. Patients will be admitted to the clinic on the third postoperative day, and their care will continue to be provided by the nurse responsible for their care as part of routine clinical practice. The researcher will not perform any additional interventions. At the same time as the group receiving the virtual reality headset intervention, the researcher will again have patients complete the Numerical Pain Scale, State Anxiety Scale, Numerical Satisfaction Scale, and Physiological Parameters Monitoring Form.

(Measurements will be taken during the preoperative period; however, patients who do not meet the inclusion criteria postoperatively will not be included in the study.)

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
postoperative pain
Tidsram: The second day after surgery, immediately before the procedure, immediately after the procedure, and 30 minutes later.

Pain intensity will be measured using a Visual Analogue Scale (VAS) ranging from 0 (no pain) to 10 (worst possible pain) immediately after the procedure. Measurements will be taken three times: on the second day after surgery, immediately before the procedure, immediately after the procedure, and 30 minutes later.

The second day after surgery, immediately before the procedure, immediately after the procedure, and 30 minutes later.

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Preoperative and postoperative anxiety levels
Tidsram: One day before surgery; the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure.

Anxiety levels will be assessed using the State Anxiety Inventory-Short Form (STAIS-S). The scale measures temporary anxiety levels. Scores range from 20 to 80. Measurements will be taken four times: one day before surgery; on the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure. Higher scores indicate higher (worse) anxiety.

One day before surgery; the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure.
Pre- and post-surgery satisfaction levels
Tidsram: One day before surgery; the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure.

Patient satisfaction will be assessed using a Visual Analog Scale (VAS) ranging from 0 (not at all satisfied) to 10 (extremely satisfied). Measurements will be taken four times: one day before surgery; on the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure. Higher scores indicate greater satisfaction.

One day before surgery; the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure.
Systolic Blood Pressure
Tidsram: On the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure.

Systolic blood pressure will be measured in millimeters of mercury (mmHg). Higher values indicate higher systolic blood pressure.

On the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure.
Diastolic Blood Pressure
Tidsram: On the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure.

Diastolic blood pressure will be measured in millimeters of mercury (mmHg). Higher values indicate higher diastolic blood pressure.

On the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure.
Pulse Rate
Tidsram: On the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure.

Pulse rate will be measured in beats per minute (beats/min).

On the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure.
Respiratory Rate
Tidsram: On the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure.

Respiratory rate will be measured in breaths per minute (breaths/min).

On the second day after surgery; immediately before the procedure; immediately after the procedure; and 30 minutes after the procedure.

Samarbetspartners och utredare

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Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

30 september 2026

Primärt slutförande (Beräknad)

1 mars 2027

Avslutad studie (Beräknad)

1 mars 2027

Studieregistreringsdatum

Först inskickad

21 september 2026

Först inskickad som uppfyllde QC-kriterierna

25 september 2026

Första postat (Faktisk)

28 september 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

3 november 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

31 oktober 2026

Senast verifierad

1 september 2026

Mer information

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