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Management of Patients With HF by Using Educational or Educational & Telephone or Telephone Interventions and Support in Cyprus (MEETTinCY)

C

Cyprus University of Technology

Status

Unknown

Conditions

Heart Failure

Treatments

Other: Pre-discharge in person education and post-discharge telephone education and support
Other: Telephone support and education post-discharge
Other: In person education on heart failure topics before discharge

Study type

Interventional

Funder types

Other

Identifiers

NCT01905176
MEETTinCY

Details and patient eligibility

About

The current trial aims to examine the effectiveness of three different types of nursing interventions, on heart failure (HF) patients' quality of life and on HF outcomes, compared to the usual care. The interventions include promotion of self-care practices through education and support; they are either provided before discharge, post-discharge through telephone, or both.

Full description

The current trial aims to examine the effectiveness of three different types of nursing interventions, on heart failure (HF) patients' quality of life and on HF outcomes, compared to the usual care. The interventions include promotion of self-care practices through education and support. HF patients admitted in the public hospitals of the Cyprus Republic are screened for eligibility. Consented patients who meet the inclusion criteria are recruited before their discharge, and are randomly allocated to one of the four groups of the trial. Patients of the three intervention groups receive educational intervention and support, before discharge or post-discharge through telephone, or both. Patients of the fourth group receive the usual care (control group). The patients' follow up period is 3 months. The main purpose of the study is to determine whether the combination of predischarge education/support and tele-management is more efficient in improving HF outcomes, rather than the in-person and telephonic components alone. Outcome measures include quality of life and HF events (re-admissions and death) and time to HF event.

Enrollment

300 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hospitalized adult patients with evidenced HF
  • Planned for discharge
  • NYHA class I-IV
  • Greek speaking
  • Able and willing to give informed consent

Exclusion criteria

  • Severe mental illness or severly impaired cognitive function
  • Patients that are to be transferred to nursing or rehabilitation homes
  • Patients unable to be contacted via telephone
  • Patients with active cancer
  • Patients on dialysis
  • Patients scheduled for surgery
  • Patients recently undergone surgery (up to 3 months)
  • Patients with less than 3 months life expectancy (end-stage)
  • Patients with chronic degenerative diseases

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

Double Blind

300 participants in 4 patient groups

Predischarge educational intervention
Experimental group
Description:
In person education on heart failure topics before discharge
Treatment:
Other: In person education on heart failure topics before discharge
Telephone educational intervention
Experimental group
Description:
Telephone support and education post-discharge
Treatment:
Other: Telephone support and education post-discharge
Combination
Experimental group
Description:
Pre-discharge in person education and post-discharge telephone education and support
Treatment:
Other: Pre-discharge in person education and post-discharge telephone education and support
Usual care (control group)
No Intervention group
Description:
Patients receive the routine care provided by the hospital which does not involve protocol driven discharge-planning

Trial contacts and locations

1

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Central trial contact

Fotini Kalogirou, MSc; Ekaterini Lambrinou, PhD

Data sourced from clinicaltrials.gov

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