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Effect of the Family-Centered Empowerment Model on Family Caregivers

Investigating the Effect of Educational Intervention Based on the Family-Centered Empowerment Model on the Burden of Care and Quality of Life of Family Caregivers of Patients with Leukemia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250118064426N1
Enrollment
66
Registered
2025-02-20
Start date
2024-04-24
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Leukemia. Malignant neoplasms, stated or presumed to be primary, of lymphoid, haematopoietic and related tissue

Interventions

Intervention 1: Intervention group: After approving the proposal and receiving the code of ethics with the ID (IR.IUMS.REC.1403.018), the researcher obtained the sampling introduction letter and submi

Sponsors

Iran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: The caregiver must have the ability to understand and learn the study material. The caregiver must be between the ages of 18 and 60. The caregiver is a close family member of the patient (father/mother, sister/brother, spouse/child). The caregiver must be involved in patient care for at least 4 hours a day. The caregiver has not participated in other similar training programs. The caregiver should not have a disabling physical or mental disorder (based on the individual's self-report). The patient the caregiver is caring for is undergoing chemotherapy or has recently received it (at least within the last 3 months). The patient the caregiver is caring for is an adult (18-60 years old). The patient being cared for by the caregiver is not in the inpatient ward (selected from among those referred to the blood clinic).

Exclusion criteria

Exclusion criteria: Incompletely completed questionnaires Absence of more than one training session Having any disabling physical or mental problem during the intervention as determined by the doctor Unexpected events such as migration or death of caregiver/patient Reluctant to participate in the study.

Design outcomes

Primary

MeasureTime frame
Care burden. Timepoint: Before the intervention and one month after the intervention. Method of measurement: Novak and Guest Caregiver Burden Questionnaire.;Quality of life. Timepoint: Before the intervention and one month after the intervention. Method of measurement: Cancer Caregiver Quality of Life Questionnaire (CQOLC).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactFatemeh Rashidi

Iran University of Medical Sciences

rashidi.fa@iums.ac.ir+98 21 2259 4440

Outcome results

None listed

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