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Active, Not Recruiting

NCT Number: NCT04005521

Randomized Study Regarding Preventive Jaw- and Swallowing Intervention for Patients With Head and Neck Cancer

The study includes patients with tumors of the oropharynx, larynx and hypopharynx scheduled to receive radiotherapy with curative intent (+/- chemotherapy). The patients will be randomized into either an intervention group (performing a preventive jaw- and swallowing exercise protocol before and during radiotherapy) or a control group no performing a exercise protocol. All patients will be encouraged to eat or drink for as long as possible during the therapy. All patients will meet with a speech-language therapist weekly during radiotherapy.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Head and neck cancer (tumors of the oropharynx, pharynx, hypopharynx and larynx)
  • Receiving radiohterpay (+/- chemotherapy) with curative intent
  • No previous trismus or dysphagia

Exclusion criteria

  • Surgery due to head and neck cancer
  • Previous treatment for head and neck cancer
  • Tracheostomized patients
  • No teeth
  • Inability to perform exercise intervention
  • Inability to independently fill out questionnaires in Swedish
  • Previous neurologic or neuromuscular disease

Treatment and study plan

Preventive intervention

Behavioral

Preventive, structured exercise protocol

Primary outcomes

  1. Maximal Interincisal opening (MIO)

    Time frame: 1 month post radiotherapy

    Jaw opening measured in millimeters. A MIO <36 mm is considered as trismus. i.e. limited jaw-opening.

  2. Swallowing ability

    Time frame: 1 month after radiotherapy

    Swallowing ability measured with Functional Endoscopic Examination of Swallowing (FEES)

Secondary outcomes

  1. Trismus and jaw related symptoms

    Time frame: Up to 5 years post radiotherapy

    Patient Reported Outcomes (PRO) measured with Gothenburg Trismus Questionnaire (GTQ). The GTQ consists of 21 items divided into 3 domains; Jaw related problems, Eating limitations and Muscular tension and eight single items concerning facial pain, limitations in mouth opening and inabilities to function on social and working contexts. The GTQ domains range from 0-100 where 0 equals to absence of symtoms and 100 equals worst possible symptoms.

  2. Dysphagia related symtoms

    Time frame: Up to 5 years post radiotherapy

    PRO measured with M.D Anderson Dysphagia Inventory (MDADI). This is a cancer-specific instrument measuring dysphagia, social function and quality of life in head and neck cancer patients. It consists of 19 items in four domains; emotional, physical, functional and global quality of life. The range for each subscale is 20-100 where 100 indicates best possible swallowing, i.e. better outcome.

  3. Health related quality of life (HRQL)

    Time frame: Up to 5 years post radiotherapy

    Measured with the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC QLQ) core questionnaire (c30). Consists of 30 items divided into six functional domains (Physical, Role, Cognitive, Emotional, and Social Functioning and Global Quality of life), three symptom scales (Fatigue, Pain, and Nausea/Vomiting) and six single items (Constipation, Diarrhea, Insomnia, Dyspnea, Appetite Loss, and Financial Difficulties). All domains range from 0-100. For the functional domains a higher score indicates good function, while for all other domains a high score indicates a high prevalence of symtoms, i.e. worse HRQL.

  4. Health related quality of life (HRQL)

    Time frame: Up to 5 years post radiotherapy

    Measured with the EORTC QLQ Head and neck module (HN35). It consists of 35 questions regarding symptoms more specific to the head and neck cancer population, and domain scores range from 0-100, where a higher score represents the prevalence of more symtoms, i.e. worse HRQL.

  5. Swallowing ability

    Time frame: Up to 5 years post radiotherapy

    Swallowing ability measured with FEES

  6. Maximal Interincisal opening (MIO)

    Time frame: Up to 5 years post radiotherapy

    Jaw opening measured in millimeters

Other outcomes

  1. Cost

    Time frame: Up to 5 years post radiotherapy

    The cost of intervention compared to usual care. Costs in Swedish crowns (SEK) for the intervention and all visits to healthcare during 5 years will be recorded.

  2. Quality of life for cost-effectiveness analysis

    Time frame: Up to 5 years post radiotherapy

    The outcomes of intervention compared to usual care using European Quality of life 5 dimensions (EQ5D).

  3. Quality Adjusted Life Years (QALY)

    Time frame: Up to 5 years post radiotherapy

    QALY is a measurement that combines health-related quality of life (HRQL) and life expectancy in one index. The index range between 0 and 1, where 0 equals death and 1 represents perfect health. Thus, 1 QALY corresponds to 1 year of perfect health. This is calculated using the EQ-5D.

  4. Incremental Cost Effectiveness Ratio (ICER)

    Time frame: Up to 5 years post radiotherapy

    Incremental cost for each QALY for the intervention group will be calculated using a Markov model which combines the costs and EQ-5D. The ICER will then be compared to the maximum willingness to pay level which is SEK 500,000 (€55,000) according to the Swedish National Board of Health and Welfare.

Sponsors and collaborators

Lead sponsor

Sahlgrenska University Hospital

Other

Registry information

Official study title

Preventive Randomized Study Regarding Jaw- and Swallowing Intervention for Patients Receiving Radiotherapy for Head and Neck Cancer: the Effect of Preventive Intervention for Trismus, Swallowing Function and Quality of Life

Acronym: HNC

Important dates

Study start
2019
Primary completion
2023
Study completion
2028
First posted
Jul 2, 2019
Registry last updated
Dec 2, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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