- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01706133
An Intervention for Elderly in Emergency Services
Elderly in Emergency Services: Effectiveness of an Intervention to Improve Health Outcomes
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
- Usual care as the comparison group
Usual care or standard refers to those processes or services that the elderly claimant receives the IMSS services network, after the acute phase of their illness has been stabilized and is defined that can be discharged from the emergency department, following clinical and therapeutic recommendations for improving their health.
- Elders risk population for emergency
The aging population brings a major change in health conditions and social conditions around the elderly, the analysis of the elderly population is considered according to functionality and risks of old age, when it comes to care services emergency, care becomes more critical as the elderly are older, have been identified adults of 70 and over as more vulnerable to health services, especially for the emergency services as they do not exhibit classic patterns to acute events of prevalent diseases.
- Functionality and dependence
The commitment of the functionality in adults older than 65 may be present in 5% of cases, while in over 70 years this figure rises to 50% or more. Functional impairment may be a "marker" of the effect of systemic disease on the patient and is also an indicator of severity of disease because it measures the ability of independence
The accumulation of normal aging characteristics define a threshold, which once pierced, tends to increase the propensity for loss of functional abilities due to aging. However, not everyone ages the same way, since factors such as inherited genetic capital, especially the accumulation of risks associated with lifestyle and work activities, and the opportunity to identify the disease in its period latency coupled with the accessibility and use of health services, can delay or exacerbate the loss of functionality and increase the dependency of the elderly.
- Quality of life of older
Frailty in the elderly is a state of increased susceptibility due to less booking multiple physiological systems resulting in lower resilience, negative energy balance, sarcopenia, decreased strength and reduced exercise tolerance. Frailty is associated with adverse health outcomes such as institutionalization, falls, reduced performance status and increased mortality.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
-
-
Distrito Federal
-
Mexico, Distrito Federal, México, 06725
- XXI Century National Medical
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Adults 70 and over.
- Both sexes
- Affiliation force in the IMSS
- Attending spontaneously or referred to the emergency department of hospitals in the study.
- Agree to participate in the study phase in observational or intervention by signed written informed consent
Exclusion Criteria:
Adults 70 and older whose income is service by:
a. A very serious acute condition with imminent risk to life and requires immediate emergency care, cataloged by the Triage system marked by the IMSS as Red or (state the patient's functional impairment characterized by high and low, with imminent risk life or the integrity and function of some of their organs and requires immediate medical attention since his arrival to the emergency room) or require emergency care (patient condition characterized by acute and severe functional impairment, life-threatening or the integrity and function of some of their organs and requires medical attention within the next 10 minutes after arrival at the emergency department).
- An automobile accident
- Burn-grade II or III
- Partial or total unconsciousness
- Severe cognitive impairment
- Individuals who do not agree to participate in the study
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Investigación de servicios de salud
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
---|---|
Sin intervención: Basal phase
Integrated measurement of all variables involved impact and frequency of prior use of health services and specifically to the emergency room, service access, patient characteristics, features for the classification of frailty, cognitive impairment and depression, why consultation, triage scale level on admission to the service and to the service variables in terms of length of stay, diagnosis and medical management, and related services with internal consultants percentage of inpatients discharged or deceased, in further analysis the researchers undertake group estimating frequency of use and the identification of factors associated with the use of emergency departments and adverse events
|
Participants who were assigned to the intervention will be evaluated jointly by the medical service by a medical specialist in geriatrics and a nurse trained in gerontology and geriatrics.
The doctor will monitor the apparition and / or aggravation of any geriatric syndromes already established by the specialty in geriatrics, namely, polypharmacy, delirium, dementia, depression, risk of falls, etc..
The nurse will monitor and follow up in four areas I. medical issues (pressure ulcers, infusion, mobility); II.
Mental and emotional state and coping strategies with hospitalization; III.
functionality, and IV.
Atmosphere (A.
Service status, architectural difficulties for mobility, bathing etc. B. Support Network, caregiver, and C. hardship)
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Change in hand grip strength (HS) as a physical performance test
Periodo de tiempo: Basal and Six months
|
A standardized technique and digital dynamometers (Exacta TM) wil lbe used, and the best result of two tests in the dominant hand will be used for analysis.
No cut-off points will be applied; instead the variable will be assessed as a continuous one with kilograms as the units of measure.
|
Basal and Six months
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Evaluation of individual and institutional impact
Periodo de tiempo: Six Months
|
Evaluate the impact of a scheme based on internal consultation geriatricians and home visiting nurses oriented elders 70 and over, in terms of individual outcomes and health services: a. Individual Impacts: a.1 Primary: • Fragility |
Six Months
|
Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Quantify hospital readmissions
Periodo de tiempo: One Year
|
Estimate the readmission to hospital adverse events in adults older than 70 years, underwent surgery and its comparison group from discharge from service
|
One Year
|
Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Carmen García-Peña, PhD, Epidemiological Research Unit and Health Services. XXI Century National Medical Center
- Silla de estudio: Sergio Sánchez García, PhD, Epidemiological Research Unit and Health Services. XXI Century National Medical Center
- Silla de estudio: Teresa Juarez Cedillo, PhD, Epidemiological Research Unit and Health Services. XXI Century National Medical Center
- Silla de estudio: Rogelio Moncada Tobias, Doctor, Emergency Service. General Hospital Zone No.2
- Silla de estudio: Nubia Franco Alvarez, Doctor, Internal Medicine. General Hospital Zone No. 2
- Silla de estudio: José García González, Master, Department of Nephrology. Regional General Hospital No. 1
- Silla de estudio: Ulises Pérez Zepeda, Master, Institute of Geriatrics
- Silla de estudio: Leslie Viridiana Robles Jiménez, Doctor, National Institute of Psychiatry
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (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
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- R-201 l-785-056
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .