The Effect of Auditory Stimulation and the "Love Glove" Technique
16 de mayo de 2026 actualizado por: Celal Bayar University
The Effect of Auditory Stimulation and the "Love Glove" Technique on Vital Signs in Unconscious Patients
The aim of this study was to determine the effect of the "love glove" intervention, combined with the voices of family members and nurses, on vital signs in unconscious patients in the intensive care unit. The following items will be used to collect research data: Patient Information Form (Appendix I), Data Recording Form (Appendix II), MP3 player, external headphones and voice recorder, latex gloves, and thermometer.
Data Collection Tools:
Patient Identification Form : A form containing patients' sociodemographic characteristics and their Glasgow Coma Scale score prior to the start of the study Data Recording Form: A form used to record patients' level of consciousness and hemodynamic parameters before and after the auditory stimulation procedure.
Methods This study is a randomized controlled trial designed to determine the effect of applying a family member's voice, a nurse's voice, and the "love glove" on vital signs in unconscious patients admitted to the intensive care unit. Following approval from the ethics committee, the study is planned to be conducted with comatose patients admitted to the hospital's intensive care unit.
Descripción general del estudio
Estado
Aún no reclutando
Condiciones
Tipo de estudio
Intervencionista
Inscripción (Estimado)
100
Fase
- No aplica
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
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MANİSAYunusemre
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Manisa, MANİSAYunusemre, Turquía (Türkiye)
- Kivan Çevik Kaya
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
No
Descripción
Inclusion Criteria:
- Patients in a coma who have been hospitalized in the intensive care unit for at least 48 hours, have a Glasgow Coma Scale score of 8 or lower,
- have no hearing problems,
- are hemodynamically stable,
- are either on mechanical ventilation or breathing spontaneously, have no history of head trauma,
- have received informed consent from their legal representative
Exclusion Criteria:
- Patients with open wounds,
- those diagnosed with brain death,
- those whose sedative or analgesic doses were adjusted during the study,
- those with severe hemodynamic instability,
- patients with latex allergies
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Cuidados de apoyo
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Doble
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Sin intervención: Control
Sin intervención
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Experimental: family member's voice
A pre-recorded message will be played and recorded for the patient's family members, featuring a prepared script that includes the patient's name, the family member's name, and their relationship to the patient, as well as information on the patient's location and phrases conveying hope and love.
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The audio recording of the patient's family member will be made in a quiet and calm room.
Care will be taken to select family members who have a strong emotional bond with the patient for the recording.
When determining which family member will be recorded, the patient's first-degree relatives will be consulted, and the family's collective decision will be taken into account; in addition to the family member being recorded, consent will be obtained from another family member who volunteers to serve as a witness for this person via a consent form.
A preliminary interview will be conducted with the family member selected for the audio recording in a suitable room, and they will be asked to recite the standard script.
Family members will be given as much time as they need to prepare for the audio recording.
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Experimental: nurse's voice
The audio recording made by the researcher will also be played for the other intervention group, to whom the nurse's voice will be played
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The audio recording containing the standard script to be read by the researcher will also be made in a quiet, calm room
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Experimental: Love glove
The group receiving the "love glove" treatment will be given a treatment involving latex gloves filled with warm water and air
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Latex medical gloves will be filled with warm water (37°C) and air to prevent pressure ulcers and provide a sensation of human touch.
The gloves will be connected to each other and placed on both of the patient's hands, and the treatment will be applied for 15 minutes.
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Experimental: family member's voice+glove of love
The patient's family members voice and the "glove of love" will be used together
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where the patient's voice and the "glove of love" are used together
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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blood pressure
Periodo de tiempo: Twice a day for 7 days
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Blood pressure were recorded on the Form before and after the blood sampling procedure.
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Twice a day for 7 days
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pulse
Periodo de tiempo: Twice a day for 7 days
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Pulse were recorded on the Form before and after the blood sampling procedure.
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Twice a day for 7 days
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oxygen saturation
Periodo de tiempo: Twice a day for 7 days
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oxygen saturation were recorded on the Form before and after the blood sampling procedure.
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Twice a day for 7 days
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Estimado)
1 de junio de 2026
Finalización primaria (Estimado)
1 de junio de 2026
Finalización del estudio (Estimado)
1 de abril de 2028
Fechas de registro del estudio
Enviado por primera vez
23 de marzo de 2026
Primero enviado que cumplió con los criterios de control de calidad
16 de mayo de 2026
Publicado por primera vez (Actual)
22 de mayo de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
22 de mayo de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
16 de mayo de 2026
Última verificación
1 de mayo de 2026
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- MCBU-K-CEVIK-006
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
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