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

BeyondSilos - Integrated Care Leading to a More Personalised and Coordinated Care, Improving Outcomes for Elderly Patients, Delivering More Effective Care and Support, and Provide More Cost Efficient Health and Social Services

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03111004
Acronym
BeyondSilos
Enrollment
1840
Registered
2017-04-12
Start date
2014-09-01
Completion date
2017-10-01
Last updated
2018-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COPD, Diabetes, Heart Failure, Stroke

Keywords

information technology, telemedicine, integrated care, MAST framework, organizational change, social care, elderly patients

Brief summary

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

Detailed description

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.

Interventions

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

Sponsors

Him SA
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

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).

Design outcomes

Primary

MeasureTime frameDescription
Change in length of the hospital stayDays 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)Change in the duration of hospitalization (calculated from admission date and discharge date) measured in days

Secondary

MeasureTime frameDescription
Patient encountersNumber 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 studyEncounters and contacts between patient and GP, Specialists, Nurse, other involved healthcare providers
WeightWeight measured in kilo grams (kg) at baseline (month 0) and at end (month 18) of study durationWeight as disease specific health status measurement
Blood pressureBlood pressure measured in mmHg at baseline (month 0) and at end (month 18) of study durationBlood pressure as disease specific health status measurement
Heart rateHeart rate measured in beats per minute (bpm) at baseline and at end of study durationHeart rate pressure as disease specific health status measurement
Oxygen saturationOxygen saturation measured in SpO2 (or %) based on measurement at baseline (month 0) and at end (month 18) of study durationOxygen saturation pressure as disease specific health status measurement
Blood glucoseBlood glucose measured in mg/dl based on measurement at baseline (month 0) and at end (month 18) of study durationBlood glucose pressure as disease specific health status measurement
HbA1cHbA1c measured in percentage (%) based on measurement at baseline and at end of study durationHbA1c pressure as disease specific health status measurement
CreatinineCreatinine measured in mg/dl based on measurement at baseline (month 0) and at end (month 18) of study durationCreatinine pressure as disease specific health status measurement
Re-hospitalisation periodDays 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)Re-hospitalisation within 30 days (calculate from admission date and discharge date) measured in days
Barthel indexBarthel index measured in index scale based on measurement at baseline (month 0) and at end (month 18) of study durationBarthel index as a generic health related / functional quality of life
Self-maintaining and instrumental activities of daily living (IADL)Self-maintaining and instrumental activities of daily living (IADL) measured in (IADL) scale based on measurement at baseline (month 0) and at end (month 18) of study durationSelf-maintaining and instrumental activities of daily living (IADL) as a generic health related / functional quality of life
Geriatric Depression Scale (GDS Short Form)GDS measured in GDSsf-scale based on measurement at baseline (month 0) and at end (month 18) of study durationGeriatric Depression Scale (GDS Short Form) as a psychological measure
Anxiety and depression based on HADSAnxiety and depression according to HADS-scale measurements based on measurement at baseline (month 0) and at end (month 18) of study durationAnxiety and depression (according to HADScale) as a psychological measure
PIRU questionnaire on user experience (selected questions) of Integrated Care (IC)User experience (PIRU) measurements based on PIRU-scale measurement at baseline and at end of study durationPIRU questionnaire on user experience of IC as a user perspectives measure
End user perception of service utility according to eCCIS (selected questions)End user perception of service utility based on eCCIS-scale measurement at baseline (month 0) and at end (month 18) of study durationEnd user perception of service utility (eCCIS) as a user perspectives measure
Carer perception of service utility according to eCCIS (selected questions)Carer perception of service utility based on eCCIS-scale measurement at baseline (month 0) and at end (month 18) of study durationCarer perception of service utility (eCCIS) as a user perspectives measure
Charlson Comorbidity Index (CCI)Charlson Comorbidity Index (CCI) measured in (a) ICD-10-CM and (b) CCI scale based on measurement at baseline (month 0) and at end (month 18) of study durationCharlson Comorbidity Index (CCI) as a generic health related / functional quality of life

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 17, 2026