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Clinical Trials in Turkey / NCT07593729
Recruiting Not applicable

Nurse-Led Caregiver Support Program in Home Palliative Care

NCT07593729 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-05-12
Last updated
2026-07-27

Condition(s) studied

Palliative CareCaregiver BurdenHome Care

Investigational drug(s) / intervention(s)

Nurse-Led Caregiver Support Program

Nurse-Led Caregiver Support Program: Participants in the intervention group will receive a structured 6-week nurse-led caregiver support program including face-to-face education, weekly telephone coaching, caregiver guidance materials, symptom management support, medication management education, stress management strategies, and healthcare utilization decision support in addition to routine home palliative care services.

Study summary

This randomized controlled trial aims to evaluate the effect of a nurse-led caregiver support program on caregiver competency and healthcare utilization among family caregivers of patients receiving home palliative care. Family caregivers in the intervention group will receive a structured 6-week nurse-led support program including face-to-face education, weekly telephone coaching, caregiver guidance materials, and decision support for symptom management and healthcare utilization. The control group will continue to receive routine home palliative care services. Primary outcome is caregiver competency. Secondary outcomes include caregiver burden, self-efficacy, patient symptom burden, emergency department visits, and hospitalizations.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult family caregivers of patients receiving home palliative care services * Age 18 years or older * Being the primary caregiver responsible for the patient's daily care * Ability to communicate in Turkish * Willingness to participate in the study Exclusion Criteria: * Professional or paid caregivers * Caregivers with severe cognitive impairment or severe psychiatric disorders * Inability to participate in follow-up assessments

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Simav Doc. Dr. Ismail Karakuyu State Hospital Simav Kütahya Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07593729 on ClinicalTrials.gov ↗ ← All trials in Turkey