Ireland
--:--IST
Active, not recruiting Not applicable

eHealth Support Tool to Improve Quality of Life in Head and Neck Cancer Survivors

NCT07426874 · tracked via the Priya Life Science Ireland tracker
Phase
Not applicable
Started
2025-09-01
Last updated
2026-02-23

Condition(s) studied

Head and Neck Cancer (H&N)

Investigational drug(s) / intervention(s)

eHealth Survivorship Support ToolControl

eHealth Survivorship Support Tool: A digital platform including: Symptom monitoring Educational modules Self-management guidance Nurse-supported remote follow-up

Control: Standard follow up

Study summary

This study evaluates the development, implementation and effectiveness of a nurse-led eHealth support tool designed to improve quality of life and survivorship outcomes among adults treated for head and neck cancer. The intervention integrates symptom monitoring, self-management education, and structured survivorship support into routine follow-up care. Outcomes will include patient-reported quality of life, symptom burden, and healthcare utilization.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: Adults ≥18 years Diagnosed with head and neck cancer Completed primary treatment (surgery, radiotherapy, chemotherapy or combination) Within 12 months post-treatment Access to smartphone/tablet/internet Able to provide informed consent Exclusion Criteria: Recurrent or metastatic disease requiring active treatment Significant cognitive impairment Inability to use digital device Non-English speakers (if tool not multilingual)

Primary outcome measure(s)

  • Quality of Life EORTC QLQ-C30 (Global Health Status scale) — Baseline, 3 months, 6 months
    Measurement Tool: EORTC QLQ-C30 (Global Health Status scale) Time Frame: Baseline, 3 months, 6 months

Trial sites (1)

FacilityCityRegionStatus
Beaumont RCSI Cancer Centre Beaumont Ireland
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 NCT07426874 on ClinicalTrials.gov ↗ ← All trials in Ireland