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NCT07173270Recruiting

Improved Oral Health in Head and Neck Cancer Survivors

Source: ClinicalTrials.gov · Last updated 3 Sept 2026

Brief summary (registry, in English)

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?

Status (registry)
Recruiting
Study type
Interventional
Enrollment
300 (estimated)
First submitted
26 Aug 2025
Start date
25 Sept 2025
Primary completion date
31 May 2035
Lead sponsor
Uppsala University
NCT number
NCT07173270

What you commit to

  • Study type: Interventional
  • Planned participants: 300
  • From 25 Sept 2025 to the primary completion date, 31 May 2035
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • cognitive impairment

Other

  • severe alcoholism
  • inability to understand the Swedish language

Who the study is looking for

  • patients (≥ 18 years)
  • diagnosed with HNC
  • scheduled for treatment with curative intent, including RT or CRT with or without surgery

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Uppsala University
Coordinator of this site? Confirm its status
UppsalaSwedenRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.