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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01772888
Other study ID # 12-103
Secondary ID
Status Completed
Phase
First received
Last updated
Start date October 2012
Est. completion date July 2019

Study information

Verified date March 2020
Source University Hospital, Geneva
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Study aims: The primary aim is to determine whether chewing efficiency, determined by a two-colour mixing ability test, and maximum bite and lip force decrease in ALS patients.


Description:

Study center: University Hospitals of Geneva Study type: Cohort study with matched controls Study population: 25 ALS patients included in the multidisciplinary cohort study of the University Hospital Geneva between October 2012 and October 2014 and followed for 3 years maximum and 25 controls, matched for age, sex and dental status.

Study duration: Inclusion from October 2012 to October 2016. Follow-up for 3 years.

Study hypothesis: Chewing efficiency, maximum bite and lip force decrease with time in ALS patients and may be a marker of texture adaptation and PEG necessity.

Study aims: The primary aim is to determine whether chewing efficiency, determined by a two-colour mixing ability test, and maximum bite and lip force decrease in ALS patients.

The secondary aims are to determine, in ALS patients, whether:

- Maximum bite and lip force decrease.

- Chewing efficiency, maximum bite and lip force decrease more in ALS patients with bulbar than with spinal onset.

- Chewing efficiency and bite force correlate with energy intakes, nasofibroscopic assessment, and a validated swallowing questionnaire.

- Saliva volume increases with time and progression of disease and influences masticatory efficiency.

- Saliva volume is associated with nasofibroscopy assessment.

Methods : Every three months, we will perform:

- As part of the ongoing cohort study (already accepted by the Ethical Committee) calculation of energy intakes through a 24h recall, nasofibroscopy, swallowing questionnaire and score of disease severity.

- As part of this study: assessment of dental status at first visit, chewing efficiency test by a with a colour mixing ability test, maximum voluntary bite and lip force, saliva volume and calculation of a 3-day dietary recall instead of a 24h recall.

Statistics: Evolutions with time and between groups, of chewing efficiency, bite and lip force will be assessed by repeated measures ANOVA. Correlations between two continuous variables will be examined by Spearman's correlation coefficients at the different time points. Correlations between a continuous variable and a binary variable (nasofibroscopic assessment) will be explored by logistic regression with mixed effect model.


Recruitment information / eligibility

Status Completed
Enrollment 25
Est. completion date July 2019
Est. primary completion date July 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- ALS patients

- > 18 years

- Participation in the cohort study

Exclusion Criteria:

- Refusal of participating in the cohort study

- Presence of PEG

Study Design


Locations

Country Name City State
Switzerland University Hospital Geneva

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Geneva

Country where clinical trial is conducted

Switzerland, 

References & Publications (1)

Schimmel M, Christou P, Herrmann F, Müller F. A two-colour chewing gum test for masticatory efficiency: development of different assessment methods. J Oral Rehabil. 2007 Sep;34(9):671-8. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary - Chewing efficiency 5 years
Secondary Lip force 5 years
Secondary Bite force 5 years
Secondary Calorie and protein intakes 5 years
Secondary Saliva volume 5 years