CClinicalTrials.gg
Active, not recruitingNCT07426874Updated Feb 23, 2026

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

An interventional study of eHealth Survivorship Support Tool and Control in Head and Neck Cancer (H&N), sponsored by Royal College of Surgeons, Ireland. Active, not recruiting at 1 site in Ireland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-02-23.

Sponsored by Royal College of Surgeons, Ireland · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 5 months after the study started (first participant enrolled Sep 2025, registered Feb 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

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.

Read the detailed description

Head and neck cancer (HNC) survivors experience significant long-term physical, functional, and psychosocial sequelae including dysphagia, speech impairment, fatigue, pain, and psychological distress. Traditional follow-up models rely on periodic clinic visits and may not adequately support self-management.

This study involves three phases:

Development of a co-designed eHealth support platform.

Implementation of the intervention within survivorship care pathways.

Evaluation of clinical effectiveness using patient-reported outcomes and healthcare utilization metrics.

The intervention integrates:

Symptom tracking Educational resources Self-management tools Structured nurse-guided follow-up

The primary hypothesis is that structured digital survivorship support will improve global quality of life compared to usual follow-up care.

02

Conditions studied

  • Head and Neck Cancer (H&N)

Keywords

  • Head and Neck Cancer
03

In context

Head and Neck Neoplasms

2,347 studies on the registry are indexed under Head and Neck Neoplasms; 553 are open to participants now.

This study's enrollment of 30 is below the median of 47 across 1,753 interventional studies indexed under Head and Neck Neoplasms.

Browse Head and Neck Neoplasms studies →

Lead sponsor

Royal College of Surgeons, Ireland is the lead sponsor of 93 studies on the registry; 44 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts 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

Exclusion Criteria:

Recurrent or metastatic disease requiring active treatment Significant cognitive impairment Inability to use digital device Non-English speakers (if tool not multilingual)

05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
30 participants (actual)

Study arms

  • Experimental
    Intervention

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

    Other: eHealth Survivorship Support Tool

  • Active comparator
    Control

    Participants receive standard survivorship follow-up as per institutional guidelines.

    Other: Control

Interventions

  • OthereHealth Survivorship Support Tool

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

  • OtherControl

    Standard follow up

06

What researchers measure

Primary outcomes

  1. Quality of Life EORTC QLQ-C30 (Global Health Status scale)

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

    Time frame: Baseline, 3 months, 6 months

07

Study locations

1 site
  • Beaumont RCSI Cancer Centre
    Beaumont, D09V2N0, Ireland
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07426874
Lead sponsor
Royal College of Surgeons, Ireland
Responsible party
Sponsor
First posted
Feb 23, 2026
Start date
Sep 1, 2025
Primary completion
Oct 12, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Feb 23, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Feb 2026. You cannot join it, but the record below documents what was studied.

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