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

H

Him SA

Status

Completed

Conditions

Diabetes
Stroke
COPD
Heart Failure

Treatments

Other: New Care

Study type

Observational

Funder types

Other

Identifiers

NCT03111004
BeyondSilos_CIP_No.621069

Details and patient eligibility

About

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

Full 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.

Enrollment

1,840 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion 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).

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.

Trial design

1,840 participants in 2 patient groups

Study Group
Description:
The Study Group receives 'new care' (integrated health and social care)
Treatment:
Other: New Care
Comparator Group
Description:
The comparator group receives usual care

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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