RecruitingNot applicableEN originalHead and neck cancer

Improved Oral Health in Head and Neck Cancer Survivors

⚠️

This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

The goal of this clinical trial is to learn if an oral care programme, designed as a multicentre two-armed randomised controlled trial (RCT), can prevent or mitigate late oral sequalae following completion of head and neck cancer (HNC) treatment, and assessing its impact on health-related quality of life (HRQoL), oral health, work ability, nutritional status, psychological well-being, and healthcare-related economic costs. The intervention consists of an oral care programme given to the intervention group (HNC survivors) from six months after the end of treatment and every three months for three years. The main questions it aims to answer are: * Does the intervention improve oral health, nutritional status, HRQoL, and reduce stress and anxiety compared with standard care? * Does the intervention reduce the duration of sick leave and improve return-to-work outcomes compared with standard care? * Is the intervention cost-effective from a health economic perspective? * Does the intervention improve patients' self-efficacy in managing their oral health and related challenges compared with standard care? * Does the intervention influence self-reported oral health, oral health-related behaviours, and oral health knowledge over time compared with standard care? * Do the effects of the intervention differ according to age, sex and sociodemographic factors? * Does the intervention affect salivary composition and salivary biomarkers over time compared with standard care?

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • •Wiek co najmniej 18 lat
  • •Rozpoznany rak głowy i szyi
  • •Leczenie zaplanowane z zamiarem całkowitego wyleczenia, z zastosowaniem radioterapii lub chemioradioterapii, z operacją lub bez niej

✗ Disqualifies

  • •Ciężkie uzależnienie od alkoholu
  • •Poważne problemy z pamięcią lub logicznym myśleniem
  • •Brak możliwości porozumiewania się w języku szwedzkim

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
September 3, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (1)

Uppsala University

Uppsala, Sweden

Trial contact

Ylva Tiblom Ehrsson, Assoc professor, RN

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 9/4/2026.

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