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The effect of telehealth early palliative care on the quality of life of patients and family caregivers in patients with advanced cancer

The effect of telehealth early palliative care on the quality of life of patients and family caregivers in patients with advanced cancer

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241225064165N1
Enrollment
168
Registered
2025-01-28
Start date
2025-01-20
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Condition 1: Breast Cancer. Condition 2: Lung cancer. Condition 3: Stomach cancer. Condition 4: Liver cancer. Malignant neoplasm of breast Malignant neoplasm of bronchus and lung Malignant neoplasm of stomach Malignant neoplasm of liver and intrahepatic bile ducts

Interventions

Intervention 1: Intervention Group: Patients with advanced cancer and their family caregivers who receive early palliative care education remotely. After being deemed eligible for participation in the

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients must be over 18 years old. They should be able to read and write in Persian. They must have access to a smartphone. They should be recognized as having advanced cancer, specifically metastatic/progressive solid tumors at stage III/IV, by an oncologist, within 8 to 12 weeks after the cancer diagnosis. Family caregivers must be over 18 years old. Family caregivers must be able to read and write in Persian.

Exclusion criteria

Exclusion criteria: Patients and family caregivers have a known diagnosis of mental illness. They are participating in another educational program (before or concurrently). They have a concurrent diagnosis of other disabling diseases (such as dementia, multiple sclerosis, or chronic kidney failure). There is uncorrected hearing loss in patients and family caregivers.

Design outcomes

Primary

MeasureTime frame
Early palliative care. Timepoint: At the beginning of the study, one month, three months after the intervention. Method of measurement: By the diagnosis of a palliative care specialist physician.

Secondary

MeasureTime frame
Quality of life of cancer patients. Timepoint: At the beginning of the study, one month, three months after the intervention. Method of measurement: 14- question chronic disease treatment - palliative care performance evaluation questionnaire.;Quality of life of family caregivers of cancer patients. Timepoint: At the beginning of the study, one month, three months after the intervention. Method of measurement: Quality of life of family caregivers of cancer patients questionnaire.;Severity of disease symptoms. Timepoint: At the beginning of the study, one month, three months after the intervention. Method of measurement: Edmonton Symptom Assessment Scale.;Depression. Timepoint: At the beginning of the study, one month, three months after the intervention. Method of measurement: Center for Epidemiologic Studies Depression Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParvaneh Asgari

Tehran University of Medical Sciences

p-asgari@sina.tums.ac.ir+98 21 5617 3975

Outcome results

None listed

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