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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 de outubro de 2026 atualizado por: 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.

Visão geral do estudo

Tipo de estudo

Intervencional

Inscrição (Estimado)

44

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos e mais velhos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Não

Gêneros Elegíveis para o Estudo

Tudo

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Cuidados de suporte
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Solteiro

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: 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.

Outros nomes:
  • Óculos de Realidade Virtual
Sem intervenção: 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.)

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
postoperative pain
Prazo: 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.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Preoperative and postoperative anxiety levels
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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.

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

30 de setembro de 2026

Conclusão Primária (Estimado)

1 de março de 2027

Conclusão do estudo (Estimado)

1 de março de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

21 de setembro de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

25 de setembro de 2026

Primeira postagem (Real)

28 de setembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

3 de novembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

31 de outubro de 2026

Última verificação

1 de setembro de 2026

Mais Informações

Termos relacionados a este estudo

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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