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Effect of education and follow up on readmission for the heart failure patients after discharge

Evaluating the effect of education and follow-up on readmission rates for the heart failure patients after discharge

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014051717727N1
Enrollment
120
Registered
2014-08-23
Start date
2014-08-23
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Related of education and follow-up on readmission rates for the Heart Failure Patients after discharge. Need for continuous supervision

Interventions

Intervention 1: Intervention group: there are two parts of intervention
the first part is Patients and their family education about the life style, drug consumption, and warning signs were performed in 20 till 25 minutes immediately after discharge, according to the educ
Prevention
Intervention group: there are two parts of intervention
Control group: Patients in control group get the routine care and had been called just every two weeks to record the information about primary data according to the control check lists and the time sp

Sponsors

Shahid Beheshti university of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria were: stabilized heart failure, literacy, tendency of the patients to participate the study, minimum age of 20, telephone access. Exclusion criteria were: stabilized psychiatric disorders, concurrent fatal disease, and severe hearing impairment.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Frequency of Hospital readmission in control and intervention groups. Timepoint: Every two weeks until three month after intervention. Method of measurement: Asking the patient.;Frequency of outpatient physician visits in control and intervention groups. Timepoint: Every two weeks until three month after intervention. Method of measurement: Asking the patient.;Drug consumption in control and intervention groups. Timepoint: Every two weeks until 3 month after intervention. Method of measurement: Asking the patient.;Improvement in control and intervention groups. Timepoint: Every two weeks until 3 month after intervention. Method of measurement: Asking the patient.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactNastaran Laal

Shahid Beheshti university of Medical sciences

laalnastaran@gmail.com; laalnastaran@sbmu.ac.ir+98 21 2243 9936

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026