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Prevention of Trismus During Radiotherapy and Quality of Life in Head and Neck Cancer Patients

Primary Purpose

Trismus

Status
Unknown status
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
TheraBite® Jaw Motion Rehabilitation System™
Sponsored by
University Hospital, Linkoeping
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Trismus focused on measuring Trismus, Cancer, Radiotherapy, Quality of life

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 or older
  • Be able to communicate and understand the Swedish language.
  • Compliance with training programme and follow-up during the study time period.
  • Planed radiotherapy dose of at least 15Gy to the jaw muscles.
  • Tooth 11 and 41 intact.

Exclusion Criteria:

  • An operation in the target area that has already affected jaw mobility.
  • Jaw measurement under 35mm.

Sites / Locations

  • Department of Radiation Oncology, Ryhov ,Sweden
  • Department of Radiation Oncology, University Hospital, Linkoping

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

TheraBite grupp

Conventional treatment

Arm Description

Outcomes

Primary Outcome Measures

Change in Jaw mobility measurement during Radiotherapy
Proportion of participants free from trismus at the end of Radiotherapy.

Secondary Outcome Measures

Change in Jaw Mobility measurement at 6 and 12 months after completed Radiotherapy
Proportion of participants free from trismus 6 and 12 months after completed Radiotherapy.

Full Information

First Posted
May 2, 2011
Last Updated
April 13, 2016
Sponsor
University Hospital, Linkoeping
Collaborators
Linkoeping University, Ryhov County Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01354548
Brief Title
Prevention of Trismus During Radiotherapy and Quality of Life in Head and Neck Cancer Patients
Official Title
Prophylactic Training for the Prevention of Radiotherapy-induced Trismus - a Randomised Study. Health-related Quality of Life up to One Year After Radiotherapy in Patients With Head and Neck Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
April 2016
Overall Recruitment Status
Unknown status
Study Start Date
February 2010 (undefined)
Primary Completion Date
April 2016 (Actual)
Study Completion Date
June 2016 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University Hospital, Linkoeping
Collaborators
Linkoeping University, Ryhov County Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Trismus (limited jaw mobility), can occur in patients undergoing radiotherapy to specific areas of the head or neck. Trismus leads to difficulty in eating, swallowing, speech and general mouth hygiene, which all have negative effects on quality of life. Research in the area of trismus is limited; it is not known exactly when trismus develops, one study suggests that some patients have experienced a diminished opening at as low doses as 15 Gy. Literature suggests benefits of a training programme, but there is a lack of evidence to support the use of a training programme during radiotherapy. The purpose of this study is to investigate the effectiveness of a training programme during and after radiotherapy, and report the incidence of trismus in patients who receive radiotherapy to the jaw muscles. The study also investigates quality of life during radiotherapy and up to one year after completed treatment. Patients who meet the criteria and give their consensus to the study are divided into two groups: Group 1: Training with TheraBite Jaw Motion Rehabilitation System, which is a portable system utilizing repetitive passive motion and stretching to restore mobility and flexibility of the jaw musculature. Individuals train five times a day. Group 2: Conventional treatment (jaw measurements once a week). If the individuals jaw mobility decreases 15% from the original start measurement, the patient is automatically offered a trainings program (as in group 1). During radiation therapy a hospital specialist dentist measures the jaw mobility once a week, thereafter at 3,6,12 months after completed Radiation Therapy. On 5 different occasions the patients are requested to complete a Quality of life questionnaire. Patient's record their training frequency in a log book.
Detailed Description
Summary of the study programme Background During Radiation therapy to the mouth, throat or trachea can fibrosis often occur in the chewing muscles round the jaw causing a development of trismus (a limited jaw mobility). Trismus can cause pain, difficulty in eating, swallowing, speech and difficulty with general mouth hygiene. Despite the fact that this condition has been documented in older literature, there is limited research in the incidence of trismus. There is need of randomised studies to investigate the prevention of trismus both under and during Radiation Therapy. Aims The specific aims of this study are to investigate the effectiveness of Prophylactic training with a muscle warm-up programme and a mechanical device (TheraBite) to prevent trismus during Radiation Therapy and one year after completed therapy. The study also aims to investigate the incidence of radiotherapy-induced trismus in patients who receive radiotherapy to the masseter, temporalis, pterygoid muscles. Finally the study investigates whether trismus affects quality of life. Methods Patients Sixty consecutive patients, from two different radiation clinics in Sweden, are randomised into the two different groups using a computer programme. Treatment procedures Intervention group: Daily training with a programme for TheraBite that trains passive movement, preceded by a warm-up programme. Mouth opening measurements are made once a week during treatment at the end of radiotherapy,three, six and 12 months after treatment. Control group: Receiving traditional radiation therapy with nursing care, measuring the patients mouth opening once a week during treatment, at the end of radiation therapy,three, six, and 12 months after treatment. The same training programme as group one is offered to this group as soon as evidence of trismus develops. This training is recorded by the patient in a log book. Weight, height, Mucositis analysis and quality of life are made before the commencement of radiation therapy, at the end of radiation therapy, three, six, and 12 months after treatment. The patient's weight is measured every week. Results The results of this study will give new and vital information that can give a basis to develop a clinical method of identifying and treating cancer patients who suffer from trismus. Thus giving new knowledge which can be used to formulate clinical practices.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Trismus
Keywords
Trismus, Cancer, Radiotherapy, Quality of life

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
TheraBite grupp
Arm Type
Experimental
Arm Title
Conventional treatment
Arm Type
No Intervention
Intervention Type
Device
Intervention Name(s)
TheraBite® Jaw Motion Rehabilitation System™
Intervention Description
A portable device which utilizes passive motion and stretching to improve mobility and flexibility of the jaw muscles and associated joints. Patients are given written and verbal information about TheraBite before the commencement of Radiotherapy. Investigators instruct on usage and maintenance of TheraBite. Patients are instructed to start a trainings pass by softening the jaw muscles with a simple exercise. The training programme consists of five stretches performed 5 times per day, each stretch held for 15 seconds, training continually during Radiation Therapy and up to one year after completion of Radiation Therapy.
Primary Outcome Measure Information:
Title
Change in Jaw mobility measurement during Radiotherapy
Description
Proportion of participants free from trismus at the end of Radiotherapy.
Time Frame
Up to 7 weeks
Secondary Outcome Measure Information:
Title
Change in Jaw Mobility measurement at 6 and 12 months after completed Radiotherapy
Description
Proportion of participants free from trismus 6 and 12 months after completed Radiotherapy.
Time Frame
6 and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 or older Be able to communicate and understand the Swedish language. Compliance with training programme and follow-up during the study time period. Planed radiotherapy dose of at least 15Gy to the jaw muscles. Tooth 11 and 41 intact. Exclusion Criteria: An operation in the target area that has already affected jaw mobility. Jaw measurement under 35mm.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Sussanne Börjeson, Med dr
Organizational Affiliation
Department of Medicine and Care, Division of Nursing Sciences, Faculty of Health Sciences, Linköping University, Sweden
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Radiation Oncology, Ryhov ,Sweden
City
Jonkoping
ZIP/Postal Code
551 85
Country
Sweden
Facility Name
Department of Radiation Oncology, University Hospital, Linkoping
City
Linkoping
ZIP/Postal Code
581 85
Country
Sweden

12. IPD Sharing Statement

Links:
URL
http://www.fou.nu/is/forss/
Description
Link to the Medical research council of Southeast Sweden
URL
http://www.cancerfonden.se/sv/Information-in-English/
Description
Link to the Swedish cancer Society

Learn more about this trial

Prevention of Trismus During Radiotherapy and Quality of Life in Head and Neck Cancer Patients

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