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Mastication DisorderNCT02822391

Oral Tactile Sensitivity in Stroke Patients

An observational study of Mastication Disorder and Stroke, run by University of Bern at 1 site in Switzerland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Orofacial impairment following stroke frequently involves a reduced chewing performance and dysphagia. This study investigated the sensitivity of oral tissues following stroke and its potential impact on chewing efficiency. The following two Null-hypotheses (H0) were tested: i. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
Conditions the study is for
Mastication Disorder, Stroke, No Problem Chewing
What is being tested?
observation
How many people
54 participants
Where
1 siteSwitzerland
Study dates
Feb 2012to Dec 2015
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Stroke-group

Who may be able to join

  • Written informed consent
  • Hospitalized for stroke rehabilitation
  • Able to undergo psychophysical testing
  • Presented with a facial impairment according to the House-Brackmann criteria ≥2

Who cannot join

  • Presented with acute pain in the oro-facial sphere (nominal question)
  • Additional neuro-muscular disease.

Trial locations and contacts

1 site in 1 country.

Switzerland1 site
  • Division of Gerodontology and Removable Prosthodontics, University Clinics of Dental Medicine, University of Geneva

    Geneva, 1205

Other trials in Switzerland

About this study

Official title: Tactile Sensitivity of the Oral Tissues and Chewing Efficiency Are Impaired in Stroke Patients

Orofacial impairment following stroke frequently involves a reduced chewing performance and dysphagia. This study investigated the sensitivity of oral tissues following stroke and its potential impact on chewing efficiency.

The following two Null-hypotheses (H0) were tested:

  1. Post-stroke patients do not show a reduced intra-oral sensitivity compared to a healthy controls. ii. Intra-oral sensitivity is not correlated to chewing efficiency.
Read the detailed description

Material and Methods:

Ethical approval was granted (Psy11-259, Psy 11-032) and written informed consent was obtained from all participants and/or their legal guardian. Patients were screened and recruited from the Division of Neurorehabilitation, Department of Clinical Neurosciences, University Hospital and University of Geneva, Geneva, Switzerland by a senior consultant neurologist (BL). Patients were included if they were hospitalized for stroke rehabilitation, were able to undergo psychophysical testing and presented with a facial impairment according to the House-Brackmann criteria ≥2 15. They were excluded if they presented with acute pain in the oro-facial sphere (nominal question) or an additional neuro-muscular disease.

For the experiments, an in-depth oral examination was performed and the number of functional premolar units (OU) was noted. A premolar tooth with occluding antagonist counts as one OU whereas a molar is considered two OU (including third molars). Participants were asked with a simple dichotomic question if they perceived a dry mouth.

Food-hoarding Food-hoarding was assessed with an ordinal Likert scale. Participants were asked if they currently "lost" foodstuff in the oral vestibule: Never (score 0), rarely (score1), occasionally (score2), frequently (score 3), very frequently (score 4) or always (score 5).

Maximum voluntary bite force Maximum voluntary Bite Force (MBF) was assessed by means of an Occlusal Force-Meter GM 10® (Nagano Keiki, Higashimagome, Ohta-ku, Tokyo, Japan), which has an 8.6 mm thick bite element. The gauge was placed in-between the first molars and the participants were asked to bite three times as hard as possible for about three seconds. The MBF was tested independently on the right and left side. For the analysis, the peak MBF of each side was noted.

Maximum voluntary lip force For the lip force measurements an oral screen (Dentaurum " Ulmer Modell " maxi, DENTAURUM GmbH\&Co.KG, Ispringen, Germany) was connected to a Dynamometer (ZP50-N, IMADA, Toyohashi, Japan). It was placed in the anterior oral vestibule and a horizontal pulling force was applied whilst the participant tried to withstand the force as long as possible. Per size, three peak recordings were averaged for analysis.

Tactile detection thresholds The tactile detection threshold (TDT) of mechanoreceptors was evaluated using psychophysical testing methods. A touch sensation was elicited using von Frey filaments (OptiHair, MARSTOCK nerv test, Schriesheim, Germany) 16. This test kit consists of 11 monofilaments of varying stiffness, which are calibrated to apply defined forces of 0.25 - 512 mN (±10%). The filaments were pushed vertically for about 1 second to the different test sites on each side (ipsi- and contra-lesional in stroke-patients and right- and left side in controls). The tests started with a supra-threshold stimulus, which was consecutively lowered until the patient did not feel the filament anymore. Following the filament with the lowest perceived pressure, the applied force was re-increased until the patient recognized the touch again. This procedure was repeated twice in the same session to find the threshold with the stair-case-method. The final threshold was calculated from the mean of the three infra- and three supra-thresholds. If the patient felt even the lowest stimulus available (0.25mN), the infra-threshold was set to 0.125mN.

Two-point discrimination To determine the patients' tactile spatial resolution, the static two-point discrimination threshold (2PD) was investigated 17. The smallest distance between two simultaneously presented punctiform stimuli was evaluated using a medical calliper (Schieblehre Zürcher Modell, 125mm, Hammacher Instrumente, Germany). The separation between the two tips ranged from 0 to 15 mm; the cut-off was set to 15 mm. A staircase method was used with descending distances. The participant was asked to indicate whether he/ she sensed one or two points and the corresponding distances were noted. The mean between those two distances was considered as individual minimum 2PD.

The 2PD tests sites were the extraoral surface of the lip (approximately half way between philtrum and oral commissure) and the dorsum of the tongue opposing the second premolar. For TDT, the mucosa of the cheek opposing the second premolar and on the linea alba was used as additional test site. Whereas these test sites were evaluated on both sides, the 2PD test was additionally applied to the tip of the tongue without side discrimination. For one particular analysis all TDT readings per participant were averaged (TDT.global).

Chewing efficiency Chewing efficiency was assessed with a previously developed and validated colour-mixing ability test, or bolus-kneading test, using chewing gum 18. The specimens used for this study were developed and produced for the 8020 Promotion Foundation (Japan) specifically for assessing masticatory performance in a research setting (Lotte™,Tokyo) and to be similar to the originally described method 19. The gum was composed of two individually packed beads (pink and azure colour) with similar hardness Shore Scale OO, Ø 2.4 mm, 1.11 N, pink beads: mean depth of indentation 0.2±0.01mm, mean Durometer 93.7; azure beads mean depth of indentation 0.1±0.02mm, mean Durometer 95.1). The two beads were manually stuck together and had a dimension of 18.8x14.2x3.9 mm; they were placed on the participant's tongue. The task was to chew the specimen for twenty cycles whilst being monitored by the operator (ED). The gum bolus was then retrieved from the oral cavity, placed into a plastic bag, pressed to a 1 mm thick wafer and both sides were scanned at 300dpi (Epson Perfection V750 Pro, Seiko Epson Corp., Japan).

The compound images of both sides were then subject to a colourimetric evaluation using the custom-built software ViewGum© (dHAL Software, Greece, www.dhal.com).

The software transposes the images to the HSI colour space and then calculates the hue value for each pixel in the pictures of the semi-automatically segmented gum wafers. If the colours are not mixed, two well-separated peaks on the hue axis are present which will gradually converge with increasing colour mixture. "Hue" is an angle in the HSI colour space, thus the circular variance of hue is defined as 1 minus the length of the average vector. ViewGum© displays the standard deviation between those colour peaks by taking the square root: SD = sqrt (Variance of Hue) 20. For consistency, the term Variance of Hue (VOH) will be used 18; it is considered as the measure of chewing performance in the context of this test - with a lower VOH indicating a higher the colour mixture and therefore a better chewing efficiency.

Statistical analysis Normality of all numerical variables was rejected with empirical cumulative distribution function and QQ-plots. Therefore, results are reported as median values ± standard deviation. The two groups (stroke, controls) were compared with exact Wilcoxon-, Mann-Whitney-tests for numerical data and Fisher's exact tests for categorical data.

Numerical and linear regression models were computed to analyse the impact of the investigated parameters on VOH. The relationship between a variable and a numerical end-point was measured with a Spearman correlation coefficient and a correlation test. In the case of a binary variable the end-point was transformed into a categorical variable that separates the values below and above the median. Odds Ratios OR and 95% Confidence Intervals (95%CI) were calculated to analyse the resulting 2x2 contingency table. All statistical tests were performed with R 3.2.2 (R Project for Statistical Computing, Vienna, Austria) by a senior bio-statistician.

Being tested
observation
Medical subject headings
Stroke, Deglutition Disorders

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • observationOther

Study groups in NCT02822391
Study groupRoleWhat they receive
Stroke-groupScreened and recruited from the Division of Neurorehabilitation, Department of Clinical Neurosciences, University Hospital and University of Geneva, Geneva, Switzerland by a senior consultant neurologist (BL). Patients were included if they were hospitalized for stroke rehabilitation, were able to undergo psychophysical testing and presented with a facial impairment according to the House-Brackmann criteria ≥2 15. They were excluded if they presented with acute pain in the oro-facial sphere (nominal question) or an additional neuro-muscular disease.
Receives: Other: observation
Control-groupSimilar to stroke group in regard to age, gender and dental state. no stroke
Receives: Other: observation

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Tactile detection threshold (0.25 - 512 mN) of mechanoreceptors of oral mucosa and lips as assessed with monofilaments of pre-defined thicknesses

    Measured: maximum 2 weeks post-stroke

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Jul 2016 (estimated)
  2. Study startFeb 2012
  3. Primary completionDec 2015
  4. Study completionDec 2015

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Case-control
Time perspective
Cross-sectional
Enrolment
54 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02822391
Sponsor's protocol ID
AVC Sens
Status last verified
Jun 2016
First submitted
21 Jun 2016
Last updated
4 Jul 2016
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

An observational study of Mastication Disorder and Stroke, run by University of Bern at 1 site in Switzerland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 4 Jul 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Switzerland. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Tactile detection threshold (0.25 - 512 mN) of mechanoreceptors of oral mucosa and lips as assessed with monofilaments of pre-defined thicknesses (time frame: maximum 2 weeks post-stroke). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Jul 2016; AzTrials last refreshed its copy on 1 Nov 2026.

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