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The effect of physician prescribed information intervention to prevent readmission of patients with heart failure

The effect of physician prescribed information intervention to prevent readmission of patients with heart failure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201109217612N1
Enrollment
120
Registered
2014-03-20
Start date
2013-11-22
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

Heart Failure. Heart failure, unspecified

Interventions

Intervention 1: In this study intervention type is information prescribed by physician in the form of written information. Patients in the intervention group receive physician prescribed information
Prevention
In this study intervention type is information prescribed by physician in the form of written information. Patients in the intervention group receive physician prescribed information in written forma
patients in control group only receive routine information given by doctor to them and do not receive physician prescribed information.

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: heart failure patient without any information about their disease and with out any source like doctor or nurse to gain information; literate ability to read and write; patient between 18 to 85; patient who want will included in this study Exclusion criteria:illiterate persons; informed persons; unconscious persons; chronic kidney patients; dialysis patients; brain patients

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Rate of readmission. Timepoint: 3, 6 and twelve month after initialization of intervention. Method of measurement: contact and questionnaire.

Secondary

MeasureTime frame
Treatment Expenses. Timepoint: Six and Twelve months after finalization of intervention. Method of measurement: contact-questionnaire.;Probable side effect(like:stress) after presentation of physician prescribed information. Timepoint: Twelve months after finilization of intervention. Method of measurement: contact-questionnaire.;Change in amount of drug or doses. Timepoint: First comparison after three months of finalization of intervention-Second comparison after six months of finalization of intervention-Third comparison after twelve months of finalization of intervention. Method of measurement: Contact-questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFaranak Kazemi Majd

Tabriz University of Medical Sciences

kazemi.majd@yahoo.com+98 914 407 9849

Outcome results

None listed

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