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Completed

NCT Number: NCT01733797

Trismus Trial of Therabite vs Wooden Spatula in Head and Neck Cancer Patients

The trial will compare exercises using Therabite® versus wooden spatulas to prevent or relieve trismus in patients with stage 3 and 4 oral/oropharyngeal cancer.

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Key information

About this study

Trismus is defined as a tightening of jaw opening. The negative impact of Trismus on the quality of life of head and neck cancer patients is well established. It affects eating, drinking, speaking and social function and is often as debilitating as any disfigurement resulting from treatment.

The use of jaw exercises using a Therabite appliance following treatment has been shown to reduce the level of Trismus in small studies. Many UK centres, however, use stacked wooden spatulas inserted between the incisors as a means of passive exercise. There is anecdotal evidence that suggests the use of exercises prior to treatment may help reduce the severity of the Trismus experienced by the patient.

This study will enrol 112 head and neck cancer patients allocated by chance to use either the Therabite or wooden spatula and patients will be asked to perform mouth exercises on a daily basis for 6 months.

There is a need to evaluate both the clinical effectiveness and cost-effectiveness of Therabite as opposed to wooden spatulas to determine whether they should be adopted as standard care in head and neck cancer patients.

In this pilot trial, the investigators will measure benefits of Therabite to patients, as compared to usual care with wooden spatulas. Mouth opening will be the key outcome for the study.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Provision of signed, written informed consent
  • Aged 18 years and older
  • Able to read and write English sufficiently to be able to complete questionnaires
  • Stage 3/4 oral and oropharyngeal cancer patients undergoing:

Primary chemoradiotherapy or Surgical free flap plus post operative radiotherapy or post operative chemoradiotherapy

  • All patients will receive 60-70 Gy in 30-35 fractions over 6 to 7 weeks to the region of the pterygoid muscles.
  • All patients will have at least some trismus as indicated by subjective tightening in the jaw.

Exclusion criteria

  • <12mm mouth opening (cannot use Therabite)
  • Anatomically unable to use Therabite for example patients who may only be partially dentate and to use the Therabite would place extreme stress on the existing teeth
  • Cognitive impairment as judged by the clinicians
  • International patients treated who will not have routine UK follow up.
  • Previous surgery or RT to the head and neck prior to this diagnosis
  • Any patient who has no subjective tightening of the jaw.

Treatment and study plan

Wooden spatula

Device

Lollipop sticks placed between incisors

Therabite

Device

Hand held device placed in mouth that exercises the jaw

Primary outcomes

  1. Change in Jaw measurement

    Time frame: Baseline, 3 months and 6 months at hopsital

    Willis bite calliper will be used to measure the jaw opening at baseline, 3 and 6 months

Secondary outcomes

  1. Adherence to intervention

    Time frame: up to 6 months

    Adherence to device use will be captured by the patient on a progress log

  2. Quality of Life

    Time frame: Baseline, 3 and 6 months

  3. Health economic analysis

    Time frame: Baseline, 3 and 6 months

    Patients hospital and service use will be captured at Baseline, 3 and 6 months during interviews with the patient.

    Units used will be days in hospital or number of appointments

Sponsors and collaborators

Lead sponsor

Brynn Chappell

Other

Collaborators

  • The Christie NHS Foundation Trust

Registry information

Official study title

Randomised Pilot Study of Therabite® Versus Wooden Spatula in the Amelioration of Trismus in Head and Neck Cancer Patients. (Trismus Trial)

Important dates

Study start
2012
Primary completion
2015
Study completion
2015
First posted
Nov 27, 2012
Registry last updated
Oct 1, 2015

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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