Mouth Opening, Prevention, Education, Nutrition (OPEN) (OPEN)
Primary Purpose
Trismus, Head and Neck Cancer
Status
Recruiting
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Trismus rehabilitation
Sponsored by
About this trial
This is an interventional supportive care trial for Trismus focused on measuring Trismus, prevention, education, nutrition, preventive rehabilitation, mouth
Eligibility Criteria
Inclusion Criteria:
- Epidermoid carcinoma of the buccal cavity, oropharynx or type 1, 2 or 3 carcinoma of cavum according to the WHO classification.
- Radiotherapy (≥ 54Gy in the oropharynx) and concomitant chemotherapy (including targeted therapies) with or without surgery.
- Patients ≥ 18 years old, understanding French.
- Patients who gave their informed consent prior to the study
Exclusion Criteria:
- Disease and/or trauma with an effect on jaw mobility with permanent trismus.
- Psychiatric non-stabilized comorbidity.
- Lack of the median and lateral incisors.
- Metastatic patient.
- Legal inability or limited legal capacity.
- Medical or psychological conditions inducing incapacity of the subject to complete the study or give his/her consent.
Sites / Locations
- ONCOGARDRecruiting
- CHU d'AmiensRecruiting
- Institut Sainte catherineRecruiting
- Centre Jean PerrinRecruiting
- Centre Regional de Lutte Contre le Cancer - Centre Val d'AurelleRecruiting
- CHU de la RéunionRecruiting
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
Interventional Step
Arm Description
The interventional step will comprise the same follow-up as the observational step, except for the addition of an early and preventive care, conducted by a specialized physiotherapist using an active exercise handbook elaborated with the patient's therapeutic education transversal Unit (Utep). This aims at increasing the patient's adhesion to the program and to limit the reduction of mouth opening and its consequences ( Trismus rehabilitation)
Outcomes
Primary Outcome Measures
Trismus prevalence
The mouth opening is measured by the distance between the upper left median incisive (n°21) and the lower left median incisive (n°31) with the Therabite Range of Motion Scale. Trismus is defined as a mouth opening of less than 35mm.
Secondary Outcome Measures
Full Information
NCT ID
NCT03979924
First Posted
June 4, 2019
Last Updated
November 29, 2022
Sponsor
Institut du Cancer de Montpellier - Val d'Aurelle
1. Study Identification
Unique Protocol Identification Number
NCT03979924
Brief Title
Mouth Opening, Prevention, Education, Nutrition (OPEN)
Acronym
OPEN
Official Title
Trismus Prevalence and Preventive Rehabilitation Associated With Therapeutic Education for Patients With Head and Neck Cancer Treated With Concomitant Radiochemotherapy
Study Type
Interventional
2. Study Status
Record Verification Date
November 2022
Overall Recruitment Status
Recruiting
Study Start Date
October 20, 2016 (Actual)
Primary Completion Date
June 2023 (Anticipated)
Study Completion Date
August 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut du Cancer de Montpellier - Val d'Aurelle
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
In France, 11 316 new cases of upper aero-digestive tract cancer were estimated in 2012. These cancers are treated with a triple-therapy combining surgery, radiotherapy and chemotherapy/targeted therapies. Treatment-induced sequelae are often burdensome: reduction in mouth opening, eventually on to trismus, limitation of lips and tongue mobility, deterioration in oral hygiene, pain due to inflammation and muscle fibrosis. Trismus is defined as a mouth opening of less than 35mm in patients with head and neck cancers. It can be induced by treatments (surgery or radiotherapy) but is also reported at the time of diagnosis, due to the local evolution of the tumour.
Management of trismus and its consequences is currently mostly based on physiotherapy of maxillary constrictions in order to limit or decrease the reduction of mouth opening in these patients. Exercise protocols have been set up and evaluated in the literature, but with various results. The benefit of a physiotherapy intervention on trismus prevalence, mouth opening, and patients' quality of life has not yet been shown.
Our hypothesis is that at least 30% of patients treated with radiochemotherapy are affected by trismus. According to the nutrition national recommendations in oncology, patients the most at-risk of loco-regional complications are those who receive radiotherapy doses of 54Gy or more in the oropharynx and concomitant chemotherapy.
It is thus essential to provide these patients with an early and preventive management of trismus and its consequences, during the whole duration of the treatment.
Detailed Description
The management of trismus and its side effects is essentially based on a re-education of maxillary constrictions to limit or reduce the loss of mouth opening in patients. Exercise protocols are in place and have been evaluated in the literature with discordant results. The beneficial effect of a rehabilitation program on the prevalence of trismus, oral opening and quality of life of patients is not yet clearly demonstrated.
Three studies did not show any significant beneficial effect of rehabilitation programs nor on the prevalence of trismus or the quality of life of patients. A 2014 randomized trial showed no benefit from a passive exercise program on trismus prevention and oral opening. Another 2011 study compared 374 patients, a control group and an intervention group following language mobility exercises, rehabilitation supervised by a physiotherapist and specific trismus prevention exercises with the help of a doctor. specific tool (Jaw Trainer) during and after radiotherapy. A third, more recent, randomized study evaluated the effect of a very comprehensive rehabilitation program consisting of a 45-minute session per week of rehabilitation with a physiotherapist, 7 exercises to be performed 5 times a day at home supplemented by chewing. chewing gum 5 times a day. These last two studies nonetheless concluded the importance of carrying out other work on the subject by working on the objectives of the studies, on the tools used, and on the implementation of the exercise program.
Also, an other study cited above does not show a significant difference in mouth opening between the two rehabilitation groups, but analyzes the adhesion and shows that it is significantly higher (59 versus 41 days) in the standard rehabilitation group, less burdensome for patients. Thus, the issue of patient adherence to active rehabilitation is real and essential to take into account in studies assessing the effect of a rehabilitation program on oral opening.
The prevalence of trismus as well as its management in physiotherapy and the effectiveness of a rehabilitation program are not clearly documented in France. Our hypothesis is that currently at least 30% of patients treated by radiochemotherapy are affected by a trismus. According to national oncology nutrition guidelines, the patients most at risk for locoregional complications are those who receive oropharyngeal ≥ 54 Gray radiotherapy doses, plus concomitant chemotherapy.
It seems essential to offer these patients early and preventive management of this symptom and its consequences, throughout the duration of treatment.
This study is all the more relevant as the progress of treatment of upper aero-digestive tract cancers have allowed an improvement in survival rates, with an increase in the number of patients living with sequelae related to treatments.
The major benefit for patients will be a decrease in the loss of mouth opening during and after treatment, with the consequent improvement of the criteria of well-being and quality of life: the resumption of a normal diet, a decrease the duration of artificial nutrition, better oral hygiene, improved speech and the recovery of mimicry. All this in order to accelerate the return to the most normal social and professional life possible.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Trismus, Head and Neck Cancer
Keywords
Trismus, prevention, education, nutrition, preventive rehabilitation, mouth
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
175 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Interventional Step
Arm Type
Other
Arm Description
The interventional step will comprise the same follow-up as the observational step, except for the addition of an early and preventive care, conducted by a specialized physiotherapist using an active exercise handbook elaborated with the patient's therapeutic education transversal Unit (Utep). This aims at increasing the patient's adhesion to the program and to limit the reduction of mouth opening and its consequences ( Trismus rehabilitation)
Intervention Type
Behavioral
Intervention Name(s)
Trismus rehabilitation
Intervention Description
The patient will be followed-up by a physiotherapist during all the whole radiotherapy treatment, with short 15-min sessions, twice a week. He/she will be trained to perform regularly and by him/herself the preventive/rehabilitation exercises than the patient will do twice a day until the end of the radiotherapy treatment. The patient will then continue, in an autonomous manner, with his/her rehabilitation.
In case of trismus occurrence, the physiotherapist will advise the patient to add a passive tool to the active exercises (Jaw Trainer, Therabite, tongue depressors,…) in order to strengthen the stretching.
Primary Outcome Measure Information:
Title
Trismus prevalence
Description
The mouth opening is measured by the distance between the upper left median incisive (n°21) and the lower left median incisive (n°31) with the Therabite Range of Motion Scale. Trismus is defined as a mouth opening of less than 35mm.
Time Frame
10 weeks after the end of radiochemotherapy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Epidermoid carcinoma of the buccal cavity, oropharynx or type 1, 2 or 3 carcinoma of cavum according to the WHO classification.
Radiotherapy (≥ 54Gy in the oropharynx) and concomitant chemotherapy (including targeted therapies) with or without surgery.
Patients ≥ 18 years old, understanding French.
Patients who gave their informed consent prior to the study
Exclusion Criteria:
Disease and/or trauma with an effect on jaw mobility with permanent trismus.
Psychiatric non-stabilized comorbidity.
Lack of the median and lateral incisors.
Metastatic patient.
Legal inability or limited legal capacity.
Medical or psychological conditions inducing incapacity of the subject to complete the study or give his/her consent.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Moussion Aurore
Phone
+33467612446
Email
aurore.moussion@icm.unicancer.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Texier Emmanuelle
Phone
0467613102
Email
emmanuelle.texier@icm.unicancer.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
kerstin faravel
Organizational Affiliation
Institut régional du Cancer de Montpellier
Official's Role
Principal Investigator
Facility Information:
Facility Name
ONCOGARD
City
Nîmes
State/Province
Gard
ZIP/Postal Code
30900
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Antoine SERRE
Phone
0430061010
Ext
+33
Email
antoineserre.oncogard@orange.fr
Facility Name
CHU d'Amiens
City
Amiens
ZIP/Postal Code
80054
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Coutte Alexandre, MD
Email
coutte.alexandre@chu-amiens.fr
Facility Name
Institut Sainte catherine
City
Avignon
ZIP/Postal Code
84918
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Calderon Benoit, MD
Email
b.calderon@isc84.org
Facility Name
Centre Jean Perrin
City
Clermont-Ferrand
ZIP/Postal Code
63011
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Biau Julian, MD
Email
julian.biau@clermont.unicancer.fr
Facility Name
Centre Regional de Lutte Contre le Cancer - Centre Val d'Aurelle
City
Montpellier
ZIP/Postal Code
34298
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marc Ychou, MD, PhD
Phone
33-4-6761-3066
Email
mychou@valdorel.fnclcc.fr
Facility Name
CHU de la Réunion
City
Saint-Pierre
ZIP/Postal Code
97448
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Gouya Jéhanne
Email
jgouya@gmail.com
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
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18213726
Citation
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Mouth Opening, Prevention, Education, Nutrition (OPEN)
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