The goal of this study is to be able to perform reliable measurements on AROM of neck and shoulders , exercise capacity, strength, MMO and functional mobility to evaluate the effectiveness rehabilitation programs in head and neck cancer survivors.
ID
Source
Brief title
Condition
- Miscellaneous and site unspecified neoplasms benign
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
reliabilty measurements:
Shoulder function (Active Range of Motion, AROM)
Neck function (Active Range of Motion, AROM)
Muscle Strength ( grip strength, shoulder elevantion strength with MRC scale,
30sec chair to stand test)
Exercise capacity (6 Minute Walking Test)
Level of physical mobility (Timed Up dan Go test)
Maximal opening of the mouth ( mm)
Secondary outcome
shoulder pain and disability : The Shoulder Disability Questionnaire (SDQ), The
Shoulder Pain and Disability Index (SPADI)
Neck pain and function: The Neck Disability Index (NDI)
Quality of life : The EuroQol 5D (EQ-5D) , The EORTC QLQ C-30.
Background summary
Survivors of head and neck cancer commonly experience treatment-related
morbidity that impairs exercise capacity, muscle strength, active range of
motion (AROM) of neck and shoulder and maximal mouth opening (MMO). These
problems limit daily activities and subsequently negatively influence Health
related Quality of Life (HrQoL). Physical therapy, as part of the
multidisciplinary team, focuses on these complaints. During treatment, 73% of
all patients report the need for physical therapy, and 23% report such needs
after 8-11 years. This could indicate that as well as during treatment, long
term survivors of head and neck cancer could benefit from physical therapy.
Physical therapy could include mobility exercises to improve maximal AROM of
neck and shoulders and training to improve exercise capacity and general muscle
strength. The evidence on physical therapy treatment modalities to improve MMO
remains indecisive or absent (functional mobility). To evaluate physical
therapy with treatment goals in AROM of neck and shoulders , exercise capacity,
muscle strength, functional mobility and MMO and to ensure adequate training
progression and intensity, repeated testing of these properties is necessary.
Study objective
The goal of this study is to be able to perform reliable measurements on AROM
of neck and shoulders , exercise capacity, strength, MMO and functional
mobility to evaluate the effectiveness rehabilitation programs in head and neck
cancer survivors.
Study design
Clinimetric study with a test-retest design.
Study burden and risks
The research takes place at a regular meeting of the Dutch head and neck
patient society. Possible participants are relatively old and possibly
vulnerable. In this study we try to take this into account as much as possible
and minimize possible risks. The research consists of two measurements during
one day (1 in the morning, 1 in the afternoon) . The total amount of time
necessary for the research is estimated between 60 and 80 minutes per
participant in total. A measurement consist of active tests, questionnaires and
the collection of demographic and patient characteristics. The physical tests
consist of measurements that have been researched and performed safely in
routine daily physiotherapy care in other vulnerable patient categories and
patients with other oncological malignancies.
With the use of the PARQwe will identify patients at risk for cardiovascular
or pulmonal problems . After completion of the research the patient gets a
report describing his scores and intepretation of physical tests to compensate
for time investment
Geert Groote plein Zuid 10
Nijmegen 6525GA
NL
Geert Groote plein Zuid 10
Nijmegen 6525GA
NL
Listed location countries
Age
Inclusion criteria
Possible participants are head and neck cancer survivors and are all members of the Dutch patient organization for head and neck cancer survicors and 18 years or older.
Exclusion criteria
Patients undergoing medical treatment for head and neck cancer.
Patient receiving palliative treatment.
Patients that are not able to speak or understand Dutch. Patient that are walking aid dependent
Patients at risk when performing maximal exercise which will be assessed before inclusion using a modified Physical Activity Readiness Questionnaire (PARQ), leading to the exclusion of willing participants who answer yes to one or more questions.
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL63632.091.17 |