- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05253508
Propagation Waves in Tactile Material Perception
February 21, 2022 updated by: Reinier Haga Orthopedisch Centrum
An Investigation of the Contribution of Proximal Vibratory Cues in Tactile Material Perception'
During the exploration of surfaces with the bare finger, vibratory signals arise and propagate through the finger and hand.
While research into mechanical and neural response characteristics has demonstrated that these signals carry rich information about touched objects and their properties, only little is known about the role these propagation waves play in human perception and to which extent the somatosensory system is able to collect information from afferents at more proximal locations than the skin-object surface.
Using ring-block anaesthesia (lidocaine) we will temporarily inhibit haptic feedback sensations of healthy participants' index finger during interactions with 3D-printed surface probes that are systematically varied in two important material dimensions, namely their roughness and hardness (elasticity), while the participants carry out a well-established psychophysical discrimination task.
The results will then be compared to a control condition without anaesthesia.
An accelerometer sensor, placed on the dorsal side of the hand, will serve to simultaneously record the propagating tactile waves.
Given their role in material perception, thermal cues will be monitored during the experiment with a thermometer and the hydration level of the fingertip skin will be measured regularly using a corneometer.
This research will allow us to understand the role of propagation waves in material perception.
It seeks to uncover some of the perceptual mechanisms that remain intact during surface discrimination of textured, compliant surfaces, while local information is temporarily inhibited.
The results will have implications for how we provide feedback about material properties for sensorimotor control to this living with prosthetic limbs.
It is hypothesised that propagation waves that arise during these haptic interactions contain behaviourally relevant information used for the discrimination of surface properties.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
15
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Karina Driller
- Phone Number: +45 30484333
- Email: k.k.driller@tudelft.nl
Study Contact Backup
- Name: Nina Mathijssen
- Phone Number: +31647208490
- Email: N.Mathijssen@rhoc.nl
Study Locations
-
-
-
Zoetermeer, Netherlands, 2725 NA
- Recruiting
- Reinier Haga Orthopedic Center
-
Contact:
- Nina Mathijssen
- Phone Number: +31647208490
- Email: N.Mathijssen@rhoc.nl
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- 18 years or older;
- No reported psychiatric or neurological disorders;
- Able to provide informed consent;
- Voluntary participation with written informed consent.
Exclusion Criteria:
- Is pregnant or currently breastfeeding;
- Has a known Lidocaine allergy;
- Is currently undergoing any other medical intervention or taking part in a study involving one;
- Has a history of finger/hand/upper limb trauma or disease;
- Has a disease affecting normal motor functioning.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: N/A
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Healthy human participants
ring-block anaesthesia with lidocaine in one of the two visits
|
A digital nerve block by injections to the base of the finger
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Change in discrimination thresholds
Time Frame: one year
|
The (statistical) difference between psychophysical measures (i.e., difference limen/discrimination thresholds) when the index finger is anaesthetised as compared to non-anaesthetized.
|
one year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2022
Primary Completion (Anticipated)
March 15, 2022
Study Completion (Anticipated)
March 30, 2022
Study Registration Dates
First Submitted
February 2, 2022
First Submitted That Met QC Criteria
February 21, 2022
First Posted (Actual)
February 23, 2022
Study Record Updates
Last Update Posted (Actual)
February 23, 2022
Last Update Submitted That Met QC Criteria
February 21, 2022
Last Verified
February 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Physiological Effects of Drugs
- Molecular Mechanisms of Pharmacological Action
- Anti-Arrhythmia Agents
- Central Nervous System Depressants
- Peripheral Nervous System Agents
- Sensory System Agents
- Anesthetics
- Membrane Transport Modulators
- Anesthetics, Local
- Voltage-Gated Sodium Channel Blockers
- Sodium Channel Blockers
- Lidocaine
Other Study ID Numbers
- NL75084.058.21
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Sensory Processing
-
Boston University Charles River CampusCompletedSensory Processing DisorderUnited States
-
University of Southern DenmarkProtac A/SRecruitingChildren | Sensory Processing DisorderDenmark
-
Uskudar UniversityHacettepe UniversityCompleted
-
The Spiral Foundation at OTA WatertownMaxwell Hurston Charitable FoundationUnknownSensory Processing DysfunctionUnited States
-
Pingale, Vidya, OTRTina S. Fletcher, EdD, MFA, OTR; Catherine Candler, PhD, OTR; Noralyn Pickens... and other collaboratorsCompletedSensory Processing Disorder | Autism | Special EducationUnited States
-
Centre Psychothérapique de NancyInstitut National de la Santé Et de la Recherche Médicale, FranceNot yet recruitingSchizophrenia | Sensory Processing Disorder
-
University of NebraskaRecruitingAutism Spectrum Disorder | Sensory Processing Disorder | Autism | Sensory Over-ResponsivityUnited States
-
National Taiwan University HospitalNational Taiwan University; National Science and Technology CouncilNot yet recruitingAutism Spectrum Disorder | Sensory Processing Disorder
-
Atlas UniversityRecruitingHip Fractures | Elderly | Sensory Processing Disorder | Sensory Disorder | Fall Injury | Falling | SensitivityTurkey
-
Dayton Children's HospitalThe Robert C. Cohn Research EndowmentCompletedAutism Spectrum Disorder | Anesthesia | Sensory Processing Disorder | Procedural AnxietyUnited States
Clinical Trials on Lidocaine 2% Injectable Solution
-
McMaster UniversitySt. Joseph's Healthcare HamiltonWithdrawnIntravenous Lidocaine for Post-Operative Pain Control in Patients Undergoing Bariatric Bowel SurgeryBariatric Surgery Candidate
-
University of British ColumbiaCompletedMigraine in Children | Posttraumatic HeadacheCanada
-
Develi Devlet HastanesiUnknownAnesthesia, Local | Patient Satisfaction | Anesthesia Recovery Period | Cataract Surgery | Anesthesia; Adverse Effect | AkinesiaTurkey
-
Menoufia UniversityRecruitingPostoperative Sore ThroatEgypt
-
University of SaskatchewanCompletedPharyngitis | Intubation, Intratracheal | Lidocaine | Ropivacaine | Post-operative Sore ThroatCanada
-
Medical University of SilesiaCompletedTemporomandibular DisorderPoland
-
Sintetica SARecruitingHernia, Inguinal | Flat FootItaly, Spain
-
Scilex Pharmaceuticals, Inc.Completed
-
Alcon ResearchTerminatedOcular Hypertension | Open-angle Glaucoma
-
Paola M Zamora MunozCompletedAcute Pain | Knee ArthroscopyMexico