Preoperative Mindfulness Training for Enhanced Hysterectomy Recovery
Mindfulness training
Manifestaciones Neurológicas+4
+ Dolor
+ Dolor postoperatorio
Estudio de Prevención
Resumen
Fecha de inicio: 20 de junio de 2023
Fecha en la que se inscribió al primer participante.This study focuses on the impact of mindfulness training before a minimally invasive hysterectomy surgery. The goal is to find out if this approach can help manage postoperative pain, which can often be challenging to treat and may lead to decreased patient satisfaction and quality of life. Traditionally, pain management has relied heavily on medicines, especially opioids. However, due to potential risks like longer hospital stays, future hospitalizations, and the risk of dependence, there's a growing interest in non-medicinal pain management methods. Mindfulness training, which involves techniques to calm the mind and reduce negative emotions, has shown promise in managing chronic pain. But its effects on acute pain, particularly post-surgery, are not well-studied. This research aims to fill that gap, investigating the benefits of mindfulness training delivered via an internet application for women undergoing hysterectomy. Participants in this study will use a mindfulness app before their surgery. The effectiveness of this intervention will be measured on the first day after surgery using a validated pain rating scale. This scale ranges from 0 to 10, with 0 representing 'No pain' and 10 indicating 'Worst possible pain'. The scores will be compared between those who used the mindfulness app and those who did not. This will help understand if mindfulness training can be a low-cost, low-risk way to improve recovery and reduce pain and stress associated with hysterectomy.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 72 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Estudio de Prevención
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Mujer
Sexo biológico de los participantes elegibles para inscribirse.A partir de 18 años
Rango de edades de los participantes que pueden unirse al estudio.Voluntarios sanos no permitidos
Indica si personas sanas, sin la condición que se estudia, pueden participar.Condiciones
Patología
Criterios
Inclusion Criteria: * Scheduled to undergo minimally invasive hysterectomy * Fluency in English and/or Spanish * Access to a device capable of running the Headspace application (smart phone or computer) Exclusion Criteria: * Minors * Hearing impairment * Inability to access Headspace app * Inability to complete baseline or postoperative surveys: Perceived Stress Scale-10 (PSS-10) or Quality of Recovery-15 (QOR-15) surveys
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.Un solo grupo de intervención está designado en este estudio
0% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
Grupo I
ExperimentalCentros del Estudio
Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.Este estudio tiene una ubicación
Montefiore Medical Center-Albert Einstein College of Medicine
The Bronx, United StatesAbrir Montefiore Medical Center-Albert Einstein College of Medicine en Google Maps