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Not yet recruitingNCT06936579Updated Apr 24, 2025

Cortical Effects of Peripheral Proprioceptive Stimulation on the Motor Evoked Potentials of the Limbs

An interventional study of proprioceptive stimulation in Healthy Subjects, sponsored by Facultat de ciencies de la Salut Universitat Ramon Llull. Not yet recruiting at 1 site in Spain. Open to participants aged 18 Years to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-04-24.

Sponsored by Facultat de ciencies de la Salut Universitat Ramon Llull · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Primary completion was expected by Jul 2025, 1 year 2 months ago, but the record still lists the study as not yet recruiting.
Phase
Not applicable
Study type
Interventional
Enrollment
31
Allocation
Randomized
Ages
18 Years to 80 Years
Sex
All
01

Study summary

Through motor muscle potentials, we will observe how a peripheral somatosensory mechanical stimulus on key limb musculature communicates signals via afferent sensory fibers that encode proprioceptive signals from muscle spindles (particularly type Ia fibers) to the somatosensory cortex at rest, confirming the integrative hypothesis of movement.

These results would support interventions aimed at addressing sensory deafferentation present in multiple health conditions related to movement disorders, where disuse or immobilization lead to changes in movement patterns and a decrease in neuronal activation in somatosensory cortex areas involved in constructing voluntary movement.

Read the detailed description

Objective: To evaluate whether a proprioceptive stimulus applied to the limb of healthy subjects activates the corticospinal pathway, compared to a condition without stimulation, through the analysis of motor evoked potentials (MEPs).

Methods: Experimental and crossover. Each participant will serve as their own control and will be assessed under both stimulation (experimental) and no-stimulation (control) conditions.The stimulus will consist of intermittent mechanical pressure on the skin located at the neuromuscular motor points (NMPs) of the upper limb (biceps muscle (B) and wrist extensors (WE)) and the lower limb (rectus femoris of the quadriceps (RFQ) and tibialis anterior (TA).Motor evoked potentials (MEPs) will be recorded from the B, WE, RFQ, and TA muscles using transcranial magnetic stimulation (TMS).The optimal stimulation point (hotspot-the area where TMS generates the highest MEP) will be identified individually for the B, WE, RFQ, and TA muscles.Participants will be recruited at the facilities of the Faculty of Physiotherapy and Nursing of Castilla-La Mancha University (UCLM), in collaboration with the Toledo Physiotherapy Research Group (GIFTO) and the Faculty of Health Sciences, Blanquerna - Ramon Llull University.

02

Conditions studied

  • Healthy Subjects
03

In context

Lead sponsor

Facultat de ciencies de la Salut Universitat Ramon Llull is the lead sponsor of 5 studies on the registry; 5 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

Inclusion Criteria:

Good health status with no history of neuromuscular injuries, surgical interventions, or trauma affecting the central or peripheral nervous system.

Not currently taking drugs or medications known to affect the central nervous system, and not pregnant at the time of testing.

No metallic or electronic implants and no history of epilepsy.

(Safety, ethical considerations, and application guidelines for the use of transcranial magnetic stimulation in clinical practice and research)

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Single (Outcomes assessor)
Enrollment
31 participants (estimated)

Study arms

  • No intervention
    Condition without proprioceptive stimulation:

    Participants will not receive the stimulus, and MEP activity will be recorded under the same motor cortex stimulation conditions.

  • Experimental
    Condition with proprioceptive stimulation 1

    Participants will receive proprioceptive stimulation through the output plunger, applied continuously for 15 seconds, with 20-second rest intervals, over a total duration of 5 minutes. MEP activity will then be recorded via motor cortex stimulation.

    Device: proprioceptive stimulation

  • Active comparator
    Condition with proprioceptive stimulation 2

    Participants will receive proprioceptive stimulation continuously during the application of TMS pulses while MEP activity is recorded.

    Device: proprioceptive stimulation

Interventions

  • Deviceproprioceptive stimulation

    Condition without proprioceptive stimulation: Participants will not receive the stimulus, and MEP activity will be recorded under the same motor cortex stimulation conditions. Condition with proprioceptive stimulation 1: Participants will receive proprioceptive stimulation through the output plunger, applied continuously for 15 seconds, with 20-second rest intervals, over a total duration of 5 minutes. MEP activity will then be recorded via motor cortex stimulation. Condition with proprioceptive stimulation 2: Participants will receive proprioceptive stimulation continuously during the application of TMS pulses while MEP activity is recorded.

06

What researchers measure

Primary outcomes

  1. Motor evoked potentials (MEPs)

    transcranial magnetic stimulation (TMS)

    Time frame: 45 minuts

07

Study locations

1 site
  • Pedro Victor López Plaza
    Barcelona, Spain
    • Pedro V López · Contact · pedrovictorlp@blanuqerna.url.edu · 932 53 32 56
    • Pedro Victor López Plaza · Principal investigator
    • Julio Gómez Soriano · Sub investigator
    • Lorenzo Escutia · Sub investigator
    • Ismael Ordoñez · Sub investigator
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 24, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06936579
Lead sponsor
Facultat de ciencies de la Salut Universitat Ramon Llull
Responsible party
Pedro Victor López Plaza (Principal Investigator,, Facultat de ciencies de la Salut Universitat Ramon Llull) — Principal investigator
First posted
Apr 20, 2025
Start date
May 20, 2025 (estimated)
Primary completion
Jul 15, 2025 (estimated)
Completion
Jul 30, 2025 (estimated)
Last update
Apr 24, 2025

Study contacts

Pedro V López Plaza
Contact
pedrovictorlp@gmail.com
932 53 32 56

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Apr 2025. You cannot join it, but the record below documents what was studied.

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