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Family focused Approach to iMprove Heart Failure care In Lebanon QualitY (FAMILY) Intervention

Family focused Approach to iMprove Heart Failure care In Lebanon QualitY (FAMILY) Intervention

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014101919593N1
Enrollment
260
Registered
2014-10-25
Start date
2013-10-31
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. Congestive heart failure

Interventions

Intervention 1: Both groups will be approached at baseline. The study will be introduced and the participants along with their family caregivers will be consented to participate. Baseline data collect
Treatment - Other
Both groups will be approached at baseline. The study will be introduced and the participants along with their family caregivers will be consented to participate. Baseline data collection will be done

Sponsors

No sponsor
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 139 Years

Inclusion criteria

Inclusion criteria: Selection Criteria Inclusion criteria: All those admitted to the site hospital for acute decompensated HF regardless of the aetiology, aged >18 years and willing to participate will be included in this study. The family member nominated by the patient should be willing to care for the patient and participate in the study. Patients with illiteracy will be included if their family caregiver is literate and can reach a proper decision in favour of their patient. Patients will be asked to finger print the consent form after a thorough explanation is provided about the intervention and adequate support is provided by the caregiver. Exclusion criteria Patients having limited life expectancy of less than 30 days, severe cognitive impairment limiting their judgement and activity, pending cardiac bypass or valve replacement surgery with limited functionality, living alone or in nursing home, and aged less than 18 years will be excluded. Also conditions that hinder the progress of the intervention such as impaired cognition or blindness of the caregiver exclude the possible participants.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Readmission rates. Timepoint: 30 days. Method of measurement: phone calls.

Secondary

MeasureTime frame
Self-care, QOL, ED presentations, health care utilization and major vascular events. Timepoint: 30 days. Method of measurement: phone calls.

Countries

Lebanon

Contacts

Public ContactHiba Deek

University of Technology Sydney

hiba.a.deek@student.uts.edu.au00610402315084

Outcome results

None listed

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