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Model for the Integral Assessment of Chronic Disease Management Supported in Information Technology and Communication.

I

Instituto de Investigacion Sanitaria La Fe

Status

Completed

Conditions

Chronic Disease

Treatments

Other: Phone-based care group
Other: Usual care group
Device: Platform NOMHADchronic

Study type

Interventional

Funder types

Other

Identifiers

NCT02447562
GECHRONIC

Details and patient eligibility

About

Controlled and Randomized Clinical trial with 3 parallel groups (intervention group with a health platform NOMHADchronic, phone-based care group, usual care group) developed in the Valencia La Fe Health Department. 495 high-complexity chronic patients will be included according to a combined recruitment based on a risk predictive model plus clinical opinion. Patients will be followed-up during 12 months in order to evaluate health-related quality of life, mortality, health consumption, health direct cost and treatment satisfaction.

Enrollment

495 patients

Sex

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥18 years old.
  • High complexity: according to a combined criteria a) predictive model of Valencia La Fe Health department for hospital resources consumption in next 12 months (probability >95%) and b) risk confirmation by a clinical team with experience on chronic patients management.
  • Participants that accept to participate in the study by the informed consent signature
  • Participants that don't meet any of the exclusion criteria

Exclusion criteria

  • Age <18 años.
  • Participants with cognitive or sensorial difficulties or with insufficient knowledge of one of the 2 official languages of Valencian Community that, according to the healthcare professional, may affect their study participation.
  • No residents or temporary residents in the Health Department
  • Homeless or participants with high-risk of social exclusion.
  • Terminal patients or in palliative care according to the SECPAL (Spanish Society of Palliative Care) criteria .
  • Community-dwelling patients
  • Inability for mobile phone management if there is a caregiver with this capability.
  • Participants without a phone line
  • Non high-complexity chronic patients according to the recruitment healthcare professional.
  • Members of the research team, workers related to the centers implied in the study or any other person directly involved in the study -
  • First degree consanguinity or similar affinity with the team members.
  • Participants already involved in case management.
  • Participants already participating in clinical trials or experimental trials.
  • Participants that don't accept to participate in the study or not signing the informed consent
  • Participants with a main diagnostic of mental diseases
  • Participants with active oncological diagnosis
  • Participants already following specific interventions for hemodialysis, organ transplanting, day hospital
  • Participants with an infectious chronic disease as unique chronic disease (HIV, BHV (Hepatitis B Virus)...)

Trial design

495 participants in 3 patient groups

G_AH
Active Comparator group
Description:
Usual care group
Treatment:
Other: Usual care group
G_SP
Other group
Description:
Phone-based care
Treatment:
Other: Phone-based care group
G_NOMHAD
Experimental group
Description:
Intervention group with a health platform NOMHADchronic
Treatment:
Device: Platform NOMHADchronic

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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