BeyondSilos - More Personalised and Coordinated Care and Improved Outcomes for Elderly Patients

Him SA1,840 enrolled

Overview

The study evaluates the impact of the new organisational models developed in the framework of the BeyondSilos pilot service in order to provide ICT supported integrated health and social care to elderly patients

The overall aim of the evaluation carried out in BeyondSilos is to identify the differences introduced by implementing ICT supported integrated care in different domains according to the MAST evaluation framework, including safety, clinical and social outcomes, resource use and cost of care, user/carer experience and organisational changes. The focus of the evaluation will be the impact of so called "horizontal" integration, which is the integration between social care and health care, and the changing organisational models for elderly patients. The hypothesis in this study is that integrated care (IC) will lead to a more personalised and coordinated care, improve outcomes for elderly patients, deliver more effective care and support, and provide more cost efficient health and social services.

Study Type

OBSERVATIONAL

Enrollment

1,840

Conditions

Heart Failure Stroke COPD Diabetes

Interventions

New CareOTHER

All settings that are in any way relevant to the provision of health and social care are integrated, including: out-of-hospital (community) services as well as hospitals, GPs' offices, community nurses, and any type of care practitioners, users' homes and volunteer service providers' offices

Eligibility

Sex: ALLMin age: 65 Years

Medical Language ↔ Plain English

Potential participants are selected by screening electronic healthcare and social care records or/and the hospital / national databases and/or during long term condition annual reviews in the community setting. If necessary, candidates are informed about the nature and the objectives of the evaluation. If a candidate passes the inclusion/exclusion criteria and signs the informed consent form, if necessary, they participate in the evaluation. Inclusion Criteria: * Age ≥65 years. * Presence of health needs specified as: Presence of heart failure, stroke, COPD or diabetes (diagnosed at hospital or at specialist visit) plus at least one additional chronic disease / condition included in the Charlson Comorbidity Index (CCI). * Presence of social needs based on Barthel Index of Activities of Daily Living and Instrumental Activities of Daily Living (IADL). * Reasonable expectation of permanence in the BeyondSilos project for the whole data collection period (18 months). * Informed consent, signed if necessary (by the subject or his/her delegate). * Capability to handle ICT equipment / devices alone, or with the help from a delegate. * Presence of good/reliable communication connection at home (internet, telephone or what is needed for the ICT connection). Exclusion Criteria: Subjects who have been registered with an active cancer diagnosis and undergoing treatment, has undergone an organ transplant, or is undergoing dialysis prior to enrolment. * Subjects in a terminal state * People with an AIDS diagnose.

Outcomes

Primary Outcomes

Change in length of the hospital stay

Change in the duration of hospitalization (calculated from admission date and discharge date) measured in days

Time frame: Days between admission and discharge of patient's admission episodes, measured based on follow up during whole length of study and accumulated at END of study (at month 18)

Secondary Outcomes

Re-hospitalisation period

Re-hospitalisation within 30 days (calculate from admission date and discharge date) measured in days

Time frame: Days between last discharge of patient and her/his re-hospitalization, measured based on follow up during whole length of study and accumulated at END of study (at month 18)

Patient encounters

Encounters and contacts between patient and GP, Specialists, Nurse, other involved healthcare providers

Time frame: Number of registered encounters/contacts between patient and GP, Specialists, Nurse, other involved healthcare providers within the timeframe based on total count in period between start (month 0) end (month 18) of study

Weight

Weight as disease specific health status measurement

Time frame: Weight measured in kilo grams (kg) at baseline (month 0) and at end (month 18) of study duration

Blood pressure

Blood pressure as disease specific health status measurement

Time frame: Blood pressure measured in mmHg at baseline (month 0) and at end (month 18) of study duration

Heart rate

Heart rate pressure as disease specific health status measurement

Time frame: Heart rate measured in beats per minute (bpm) at baseline and at end of study duration

Data from ClinicalTrials.gov

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