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Early early palliative care in patients with heart failure

The effect of early tele-palliative care on patinets with heart failure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20100725004443N29
Enrollment
50
Registered
2021-11-14
Start date
2022-01-20
Completion date
Unknown
Last updated
2023-03-13

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

Conditions

Patients with heart failure. Heart failure

Interventions

Intervention 1: Control group: After the initial visit, which will be performed jointly by a heart failure and transplant fellowship and a researcher, patients will be offered routine care in heart fa

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Definitive diagnosis of heart failure by a physician Diagnosis of heart failure in less than five years New York Heart Association (NYHA) class II / III or American College of Cardiology stage B / C of heart failure Ability to read and write Persian language Access and ability to use smart phones Absence of diagnosed cognitive disorders Absence of irreversible vision and hearing disorders Absence of comorbid disease that requires specialized palliative care such as cancer

Exclusion criteria

Exclusion criteria: Death or withdrawal of participants from the study Lack of cooperation during the research (non-participation in two consecutive webinars or non-participation in Social Media Groups) The patient enter the acute phase of the disease

Design outcomes

Primary

MeasureTime frame
Quality of life. Timepoint: Before the intervention, immediately after ending the intervention. Method of measurement: Persian version of the Kansas City Cardiomyopathy Questionnaire (PKCCQ) and Functional Assessment of Chronic Illness Therapy–Palliative-14 (FACIT-Pal-14).

Secondary

MeasureTime frame
Mood Status (Anxiety and Depression). Timepoint: Before the intervention, immediately after ending the intervention. Method of measurement: Hospital Anxiety and Depression Scale (HADS).;Number and duration of emergency hospital readmission of patients. Timepoint: immediately after ending the intervention. Method of measurement: Self-Report of Patients.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArvin Mirshahi

Tehran University of Medical Sciences

mirshahiarvin13750@gmail.com+98 21 6105 4000

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 11, 2026