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Home care is the assistance provided at home to those who can not travel to their Health Center. There are multiple studies on models of home care and many discrepancies about the impact that preventive home visits can have. Hypothesis: home care is expected to be better if performed by a team dedicated exclusively to the home patient, than to the traditional model, where the patient is assisted by the team that cares for the rest of the community.
Goals:
Main: determine the difference in median cumulative days of hospital admission in 12 months.
Secondaries:
Full description
Our purpose will be to compare 2 models of home care corresponding to 2
Primary Care Centers (EAP):
HYPOTHESIS. A care group dedicated exclusively to the ATDOM patient with what it entails in dedication of time and specific knowledge could get better results in health, optimize health resources and at the same time achieve greater satisfaction and quality of life to these patients. That is why our hypothesis will be that it is expected that the patient's global assistance attended from Primary Care in your home is better if it is performed by a Primary Care team trained for it with exclusive dedication to this type of patient, that, with the traditional model, where the patient that is attended at home is assisted by the clinical team that serves the rest of the community.
OBJECTIVES Main objective The main objective will be the comparison of the two models of home care in Primary care previously described by the difference in the average number of days hospitalized for 12 months among the people served in an integrated model of home care and among those served in a functional model. 3.2 Secondary objectives We will analyze them under a triple vision AIM, triple goal, better health, better care, lower costs, -effectiveness, efficiency and experience in people's health-
Comparison of both models in terms of self-perception in patients' health included in the preventive home care program, the patient's experience in attention to their health and overload of the caregiver.
-Results in efficiency and resource utilization: comparison in professional assistance, consumption of intermediate resources, consumption of social products, quality in the prescription.
METHODOLOGY OF THE STUDY.
To the subjects of this obtained sample, a telephone call will be made inviting them to participate in the study, agreeing a visit by the doctor or nurse responsible for the patient and the subject of the project will be informed. In the agreed view, will give the informed consent and the information sheet to the patient. Once signed in informed consent by the subject or in case of patients with deterioration cognitive, by the caregiver, the self-administered scales EuroQOL and IEXPACto the patient, in the case of patients with cognitive impairment, at caregiver and the Zarit questionnaire to the main caregiver so that complete They will be given an envelope to enter the completed scales that will be delivered closed to the healthcare professional. Fragility will be measured with instrument of Gérontopole at that time. These scales will be redelivered the patient and the caregiver at the end of the study, after 2 years, with the same methodology.
It is considered inevitable that professionals know how to measure themselves since they have their collaboration for the delivery of informed consent and information sheet to patient and the EuroQol, IEXPAC and Zarit scales and calculation of fragility index.
There will be 2 training sessions for healthcare professionals on the project of the study and the use of the scales they will deliver. Losses of selection of the sample are considered to the subjects or main caregivers, in the case of subjects with cognitive impairment, who do not sign informed consent.
Every 6 months the researchers will contact the subjects by telephone participants of the study (each of their Primary Care Center) and on that call will proceed to question about possible admission to private hospitals, stay in day centers or answer questions or provide information about the study. Study groups.
They are the following:
A control group of patients included in the Home Care program of the ABS Gran Sol where11 healthcare teams work with 241 patients in total in the Home care program (date December 2016) And a study group, of patients included in the Home Care program of ABS Apenins, the which have a healthcare team that works exclusively for home care with 113 patients (date December 2016) Study sample. Patients will be included who are in the Home care program and who comply with the Inclusion and exclusion criteria.
Enrollment
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Inclusion criteria
-Patients of 65 or more years, with or without cognitive impairment, that during the period of recruitment are new or existing users in a home care program long duration of the centers participants.
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
354 participants in 2 patient groups
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Central trial contact
Carolina Burgos Diez; Sebastià Santaeugènia González
Data sourced from clinicaltrials.gov
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