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comparison the effect of telenursing and not follow-up on clinical status of heart failure patients

comparison the effect of telenursing and not follow-up in caregiver of heart failure patients on self-care behaviors and clinical status of patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016080829184N2
Enrollment
66
Registered
2016-08-27
Start date
2015-09-23
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

Heart Failure. Cardiac, heart or myocardial failure NOS

Interventions

Intervention 1: Intervention- group 2: Receive educational plan and continuum phone follow-up. Intervention 2: Intervention- group 1: Receive educational plan. Intervention 3: Control group: Do not re
Rehabilitation
Intervention- group 2: Receive educational plan and continuum phone follow-up
Intervention- group 1: Receive educational plan
Control group: Do not receive intervention

Sponsors

Vice Chancellor for Research of Abadan School of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: class II and class III of heart failure that confirmed by physician based on New York Heart Association criteria; age 40 years or greater; absence of major psychiatric disorder; absence of series diseases such as musculoskeletal disorders, cancer, unstable angina, heart attack in last month; be available the caregiver in home; caregiver be able to speak and read Persian; caregiver be available for calling. Exclusion criteria: caregiver not be available for calling in determination times.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Self-care behaviore. Timepoint: Before intervention- 3 months after intervention. Method of measurement: Self-care behavior in heart failure questionnaire.

Secondary

MeasureTime frame
Exercise tolerance. Timepoint: Before intervention-3 months after intervention. Method of measurement: Six minutes walking test.;Dyspnea. Timepoint: Before intervention-3 months after intervention. Method of measurement: Dyspnea Borg scale.;Fatigue. Timepoint: Before intervention-3 months after intervention. Method of measurement: Fatigue severe scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMeryam Heidari

Abadan School of Medical Sciences

heidari-ma@ajums.ac.ir; heidari.maryam84@yahoo.com+98 61 5326 5364

Outcome results

None listed

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