Effect of Complementary and Alternative Medicine on Pain Among Inpatients
The proposed study has 3 aims: 1) quantitatively describe a model for delivering complementary and alternative medicine (CAM) therapies to understand the selection of patients and CAM therapies used for pain management, 2) examine the effects of selected CAM therapies on immediate change in pain, and 3) examine the effects of selected CAM therapies on duration of pain change.
Positive results from this study will assist hospitals in the integration of usual care and CAM therapy for pain reduction. Findings may also drive future research on the cost effectiveness of these therapies for pain management, as well as the impact on patient outcomes such as length of stay and use of narcotics.
Descripción general del estudio
Estado
Condiciones
Tipo de estudio
Inscripción (Actual)
Contactos y Ubicaciones
Ubicaciones de estudio
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Minnesota
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Minneapolis, Minnesota, Estados Unidos, 55407
- Abbott Northwestern Hospital
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Método de muestreo
Población de estudio
Descripción
Aims 1 and 2 Inclusion Criteria:
- Admission to Abbott Northwestern Hospital
- Consent to release of electronic health record for research purposes
- 18 years of age or older
- Length of stay greater than 24 hours
Aims 1 and 2 Exclusion Criteria:
- None
Aim 3 Inclusion Criteria:
- Admission to Abbott Northwestern Hospital
- Length of stay greater than 24 hours
- 18 years of age or older
- Consent to release of electronic health record for research purposes
- Received CAM therapy in current hospitalization
- Pain level of 1 or greater at the pre-treatment assessment by practitioner
- English-speaking
- Integrative medicine therapy ended between 9:00 am and 4:00 pm
Aim 3 Exclusion Criteria:
- Refuses consent
- Unable to provide consent due to competency concerns
- Has declined study participation 3 times during current hospitalization
- Has hard declined during current hospitalization
- Has been approached 6 times during current hospitalization
- Has been approached to consent earlier that day
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Model of delivering CAM therapies
Periodo de tiempo: Up to 4 years
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Quantitatively describe a model for delivering CAM therapies to understand selection of patients and CAM therapies used for pain management.
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Up to 4 years
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Effects of selected CAM therapies on immediate change in pain
Periodo de tiempo: CAM Visit (30-45 minutes)
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We will examine the effectiveness of CAM therapies on self-reported (11 point scale) pain measured just before and immediately after service delivery.
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CAM Visit (30-45 minutes)
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Effects of selected CAM therapies on duration of pain change.
Periodo de tiempo: 5 hours
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We will examine the effectiveness of CAM therapies on repeated measures of self-reported pain over several hours after therapy to assess the distribution and decay of the pain change effect.
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5 hours
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Jeffery Dusek, PhD, Allina Health
Publicaciones y enlaces útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
- AT006518-01
- R01AT006518-01 (Subvención/contrato del NIH de EE. UU.)
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