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Clinical Trials in Turkey / NCT07654998
Recruiting Not applicable

Mobile Health Application for Family Caregivers in Home Palliative Care

NCT07654998 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-06-10
Last updated
2026-07-27

Condition(s) studied

Palliative CareCancerCaregiver

Investigational drug(s) / intervention(s)

Mobile Health Application

Mobile Health Application: Participants in the intervention group will receive access to a mobile health application developed for family caregivers of patients receiving home palliative care. The application includes educational modules on palliative care and symptom management, daily care skills, medication management, nutrition and hygiene, pressure injury prevention, caregiver self-care, stress management, problem-solving, and healthcare utilization decision support. Participants will use the application for 6 weeks in addition to routine home palliative care services.

Study summary

Family caregivers play a central role in providing daily care for patients receiving home palliative care. However, caregiving responsibilities may lead to increased burden, stress, and difficulties in symptom management and care coordination. Mobile health (mHealth) interventions may provide accessible education, symptom monitoring, and decision-support resources to improve caregiver outcomes and patient care.

The aim of this randomized controlled trial is to evaluate the effectiveness of a mobile health application developed for family caregivers of patients receiving home palliative care. The primary outcome is caregiver competence. Secondary outcomes include caregiver burden, self-efficacy, patient symptom burden, emergency department visits, and hospitalizations.

A total of 120 family caregivers will be randomly assigned to either the intervention group, which will use the mobile health application for 6 weeks in addition to usual care, or the control group, which will receive usual care alone. Outcomes will be assessed at baseline, post-intervention (Week 6), and follow-up (Week 18).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Family caregiver of a patient receiving home palliative care services. * Aged 18 years or older. * Providing unpaid care to the patient for at least 3 months. * Able to read and understand Turkish. * Owns or has regular access to a smartphone compatible with the mobile application. * Willing to participate and provide written informed consent. Exclusion Criteria: * Professional or paid caregivers. * Participation in another structured caregiver support program during the study period. * Cognitive, visual, or hearing impairments that would prevent effective use of the mobile application. * Inability to complete study assessments. * Withdrawal of consent at any stage of the study.

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 NCT07654998 on ClinicalTrials.gov ↗ ← All trials in Turkey