Trismus Trial of Therabite vs Wooden Spatula in Head and Neck Cancer Patients
Primary Purpose
Oropharyngeal Cancer, Oral Cancer
Status
Completed
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
Wooden spatula
Therabite
Sponsored by
About this trial
This is an interventional prevention trial for Oropharyngeal Cancer focused on measuring Trismus, Therabite, Wooden spatula, Head and Neck cancer
Eligibility Criteria
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.
Sites / Locations
- Queen Elizabeth Hospital
- Queen Victoria Hospital
- Aintree University Hospitals NHS Foundation Trust
- The Christie NHS Foundation Trust
- York Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Wooden spatula
Therabite
Arm Description
Outcomes
Primary Outcome Measures
Change in Jaw measurement
Willis bite calliper will be used to measure the jaw opening at baseline, 3 and 6 months
Secondary Outcome Measures
Adherence to intervention
Adherence to device use will be captured by the patient on a progress log
Quality of Life
Health economic analysis
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
Full Information
NCT ID
NCT01733797
First Posted
November 19, 2012
Last Updated
September 30, 2015
Sponsor
Brynn Chappell
Collaborators
The Christie NHS Foundation Trust
1. Study Identification
Unique Protocol Identification Number
NCT01733797
Brief Title
Trismus Trial of Therabite vs Wooden Spatula in Head and Neck Cancer Patients
Official Title
Randomised Pilot Study of Therabite® Versus Wooden Spatula in the Amelioration of Trismus in Head and Neck Cancer Patients. (Trismus Trial)
Study Type
Interventional
2. Study Status
Record Verification Date
September 2015
Overall Recruitment Status
Completed
Study Start Date
December 2012 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
August 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Brynn Chappell
Collaborators
The Christie NHS Foundation Trust
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
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.
Detailed Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Oropharyngeal Cancer, Oral Cancer
Keywords
Trismus, Therabite, Wooden spatula, Head and Neck cancer
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
71 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Wooden spatula
Arm Type
Experimental
Arm Title
Therabite
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Wooden spatula
Intervention Description
Lollipop sticks placed between incisors
Intervention Type
Device
Intervention Name(s)
Therabite
Intervention Description
Hand held device placed in mouth that exercises the jaw
Primary Outcome Measure Information:
Title
Change in Jaw measurement
Description
Willis bite calliper will be used to measure the jaw opening at baseline, 3 and 6 months
Time Frame
Baseline, 3 months and 6 months at hopsital
Secondary Outcome Measure Information:
Title
Adherence to intervention
Description
Adherence to device use will be captured by the patient on a progress log
Time Frame
up to 6 months
Title
Quality of Life
Time Frame
Baseline, 3 and 6 months
Title
Health economic analysis
Description
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
Time Frame
Baseline, 3 and 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Prof Slevin
Organizational Affiliation
The Christie NHS Foundation Trust
Official's Role
Study Chair
Facility Information:
Facility Name
Queen Elizabeth Hospital
City
Birmingham
ZIP/Postal Code
B15 2TH
Country
United Kingdom
Facility Name
Queen Victoria Hospital
City
East Grinstead
ZIP/Postal Code
RH19 3DZ
Country
United Kingdom
Facility Name
Aintree University Hospitals NHS Foundation Trust
City
Liverpool
ZIP/Postal Code
L9 7AL
Country
United Kingdom
Facility Name
The Christie NHS Foundation Trust
City
Manchester
ZIP/Postal Code
M20 4BX
Country
United Kingdom
Facility Name
York Hospital
City
York
ZIP/Postal Code
YO31 8HE
Country
United Kingdom
12. IPD Sharing Statement
Citations:
PubMed Identifier
29602860
Citation
Lee R, Molassiotis A, Rogers SN, Edwards RT, Ryder D, Slevin N. Protocol for the trismus trial-therabite versus wooden spatula in the amelioration of trismus in patients with head and neck cancer: randomised pilot study. BMJ Open. 2018 Mar 30;8(3):e021938. doi: 10.1136/bmjopen-2018-021938.
Results Reference
derived
PubMed Identifier
29526341
Citation
Lee R, Yeo ST, Rogers SN, Caress AL, Molassiotis A, Ryder D, Sanghera P, Lunt C, Scott B, Keeley P, Edwards RT, Slevin N. Randomised feasibility study to compare the use of Therabite(R) with wooden spatulas to relieve and prevent trismus in patients with cancer of the head and neck. Br J Oral Maxillofac Surg. 2018 May;56(4):283-291. doi: 10.1016/j.bjoms.2018.02.012. Epub 2018 Mar 9.
Results Reference
derived
Links:
URL
http://www.christie.nhs.uk/
Description
Christie NHS website
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Trismus Trial of Therabite vs Wooden Spatula in Head and Neck Cancer Patients
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