- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07437469
Ritmos Binaurales para la Reducción del Dolor y la Ansiedad Postoperatorios
Ritmos Binaurales frente a Música de Elección para el Dolor Postoperatorio Temprano tras Artroplastia Total de Rodilla y Cadera Ambulatoria: Un Ensayo Controlado Aleatorizado
To deliver a 30-minute binaural beats audio intervention in PACU and collect pain and anxiety outcomes immediately following surgery, and 4 hours following surgery completion in adults undergoing ambulatory total knee arthroplasty and total hip arthroplasty (TKA and THA).
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Andrew R Moya, MD
- Número de teléfono: 1786-856-6463
- Correo electrónico: arm577@miami.edu, doc.a.moya1@gmail.com
Ubicaciones de estudio
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Florida
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Miami, Florida, Estados Unidos, 33132
- Reclutamiento
- Univeristy of Miami Health System
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Investigador principal:
- Victor H Hernandez, MD
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Contacto:
- Andrew R Moya, MD
- Número de teléfono: 786-856-6463
- Correo electrónico: arm577@miami.edu
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-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- American Society of Anesthesiologists Physical Status Classification System (ASA) 1-3
- Spinal anesthesia
- Patients receiving nerve-block in Post-Anesthesia Care Unit (PACU)
- Primary total hip or total knee arthroplasty
Exclusion Criteria:
- Moderate-severe hearing impairment or use of hearing aids
- History of significant tinnitus, active delirium, chronic high-dose opioid therapy (>60 MME/day baseline)
- Major psychiatric pathology
- General anesthesia
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Binaural Beats (BB)
Participants assigned to this arm will listen to a 30-minute binaural beats audio session at a comfortable volume through standardized over-ear headphones while in the post-anesthesia care unit (PACU). The audio will use a primary target frequency of 10 Hz (alpha range), created using soft sine-wave carriers in the 200-600 Hz range that generate a 10 Hz interaural difference (e.g., 400 Hz left ear / 410 Hz right ear). Volume will be set at a comfortable conversational level (~55-65 dBA) and may be adjusted by the participant. The session will begin within 15 minutes of PACU arrival. Participants may stop the audio at any time. |
30-minute binaural beats audio session targeting 400 and 410 hertz (Hz) alpha 400 hertz (Hz) in one ear 410 hertz (Hz) in other ear frequency delivered through standardized headphones in the PACU. |
|
Comparador activo: Music of Choice (MOC)
Participants in this arm will receive usual postoperative care in the post-anesthesia care unit (PACU) and may listen to music of their choice using standardized headphones. They will select their preferred music and listen for 30 minutes at a comfortable volume (~55-65 dBA), which they may adjust as needed. No binaural beat frequencies will be used. Music listening is optional and may be stopped at any time. |
Usual postoperative care in addition to patient-selected music using standardized headphones |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Change in Pain Score Numeric Pain Rating Scale (NPRS)
Periodo de tiempo: Baseline (pre-operative) to 4 hours post-operation.
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Pain intensity will be measured using the Numeric Pain Rating Scale (NPRS), a validated 0-10 scale where 0 = no pain and 10 = worst imaginable pain. Change will be calculated as the difference between the pre-operative NPRS score and the NPRS score obtained 4 hours after surgery. Higher scores indicate greater pain intensity. |
Baseline (pre-operative) to 4 hours post-operation.
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Change in Anxiety Score State-Trait Anxiety Inventory (STAI-S)
Periodo de tiempo: Baseline (pre-operative) to 4 hours post-operation.
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Anxiety will be measured using the State-Trait Anxiety Inventory - State Subscale (STAI-S). The STAI-S consists of 20 items scored from 1 to 4, producing a total score range of 20-80, with higher scores indicating greater state anxiety. Change will be calculated as the difference between the pre-operative STAI-S score and the STAI-S score obtained 4 hours after surgery. |
Baseline (pre-operative) to 4 hours post-operation.
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Total Opioid Consumption in the Post-Anesthesia Care Unit (PACU) (MME)
Periodo de tiempo: From PACU arrival (time 0) until PACU discharge (typically 1-4 hours post-operation)
|
Total opioid use administered during the post-anesthesia care unit (PACU) stay will be recorded, including all intravenous and oral opioid medications. All doses will be converted to morphine milligram equivalents (MME) using standard Centers for Disease Control and Prevention (CDC) conversion factors. Unit of Measure: Morphine milligram equivalents (MME) |
From PACU arrival (time 0) until PACU discharge (typically 1-4 hours post-operation)
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Postoperative Vital Signs Heart Rate
Periodo de tiempo: Every 30 minutes from PACU arrival until PACU discharge (approximately 1-4 hours post-operation).
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Heart rate (beats per minute) recorded at fixed 30-minute intervals during PACU recovery. Values will be abstracted from the electronic medical record. |
Every 30 minutes from PACU arrival until PACU discharge (approximately 1-4 hours post-operation).
|
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Patient Satisfaction Score
Periodo de tiempo: Measured once during the PACU stay, at the earliest feasible time point up to 4 hours post-operation
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Patient satisfaction with the postoperative experience will be measured using a 5-point Likert scale, where 1 = very dissatisfied and 5 = very satisfied. Unit of Measure: Likert score (1-5) |
Measured once during the PACU stay, at the earliest feasible time point up to 4 hours post-operation
|
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Postoperative Vital Signs Blood Pressure
Periodo de tiempo: Every 30 minutes from PACU arrival until PACU discharge (approximately 1-4 hours post-operation).
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Systolic and diastolic blood pressure (millimeters of mercury) recorded at fixed 30-minute intervals during PACU recovery. Values will be abstracted from the electronic medical record. |
Every 30 minutes from PACU arrival until PACU discharge (approximately 1-4 hours post-operation).
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Postoperative Vital Signs Respiratory Rate
Periodo de tiempo: Every 30 minutes from PACU arrival until PACU discharge (approximately 1-4 hours post-operation).
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Respiratory rate (breaths per minute) recorded at fixed 30-minute intervals during PACU recovery. Values will be abstracted from the electronic medical record. |
Every 30 minutes from PACU arrival until PACU discharge (approximately 1-4 hours post-operation).
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Victor H Hernandez, MD, MSc, University of Miami
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 20251389
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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