Primary Objective: To evaluate the feasibility and test-retest reliability of the Swallowing Performance EATing and drinking (SPEAT)-test in assessing swallowing function. Secondary Objectives: - To explore the intra- and inter-rater reliability and…
ID
Source
Brief title
Condition
- Other condition
Synonym
Health condition
Slikproblemen
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Feasibility and test-retest reliability of the SPEAT-test.
Secondary outcome
Inter- and interrater reliability and validity
Normal values of the SPEAT-test among healthy individuals within the age range
of head and neck cancer patients.
Background summary
Despite the wide range of possible assessment methods for swallowing function,
the correlation between the objective and subjective assessment methods seem
poor. This suggests that the present objective tools do not assess the same
aspects of swallowing and eating in daily life as the subjective measures. As
an extension of the timed 100mL water swallow test (WST), we developed the
Swallowing Performance EATing and drinking (SPEAT)-test which includes the
measurement of time needed to consume three boluses of different consistencies.
It is an easily accessible test, requiring minimal equipment and time and can
possibly be used to objectify, evaluate and monitor swallowing function as well
as giving insight in the participation level (ICF-code) of eating and drinking
in daily life.
Study objective
Primary Objective: To evaluate the feasibility and test-retest reliability of
the Swallowing Performance EATing and drinking (SPEAT)-test in assessing
swallowing function.
Secondary Objectives:
- To explore the intra- and inter-rater reliability and validity of the
SPEAT-test.
- To explore the normal values of the SPEAT-test among healthy individuals
within the age range of head and neck cancer patients.
Study design
In order to evaluate the reliability, the SPEAT-test will be performed in 80
subjects of which 40 have swallowing problems and 40 are healthy volunteerd.
Each subject will perform the test three times and a film recording of one test
will be evaluated three times. Also, outcome measures will be collected in
order to evaluate validity of the test.
Study burden and risks
The burden to the patient mainly includes the time it takes to complete the
assessment which is 75 minutes.
Plesmanlaan 121
Amsterdam 1066 CX
NL
Plesmanlaan 121
Amsterdam 1066 CX
NL
Listed location countries
Age
Inclusion criteria
- Patients treated for head and neck cancer
- Patients who will receive a videofluoroscopy as part of standard care
- Patients with dysphagia according to the Speech Language Pathologist
Exclusion criteria
No (history of) swallowing problems
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 | NL62178.031.17 |