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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05730166
Other study ID # MechCPM2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date February 15, 2023
Est. completion date April 21, 2023

Study information

Verified date May 2023
Source Universidad Rey Juan Carlos
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The objective is to estimate the effects on pain thresholds of a painful mechanical stimulus on the upper trapezius at moderate intensity compared to mild intensity or non-painful.


Description:

The mechanical stimulus produced in manual therapy (MT) techniques elicits neurophysiological responses within the peripheral and central nervous system responsible for pain inhibition. Almost all types of MT elicit a neurophysiological response that is associated with the descending pain modulation circuit. But it has not been demonstrated whether this inhibition occurs through a conditioned pain modulation mechanism induced by painful mechanical stimulation that is carried out with manual therapy techniques.


Recruitment information / eligibility

Status Completed
Enrollment 24
Est. completion date April 21, 2023
Est. primary completion date April 17, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - healthy male or female between 18 and 65 years - Free of pain and with no history of chronic pain Exclusion Criteria: - Pregnant or having given birth within the last year

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Mechanical Conditioning stimulus
Mechanical stimulus on the upper trapezius of the non-dominant side.

Locations

Country Name City State
Spain Universidad Rey Juan Carlos Alcorcón Madrid

Sponsors (1)

Lead Sponsor Collaborator
Josue Fernandez Carnero

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from Baseline in Tibialis Anterior Pressure Pain Threshold (PPT) to immediate post-conditioning stimulus PPTs will be assessed on the dominant side over the tibialis anterior muscle using a digital algometer (Wagner instruments, Greenwich, CT, USA). Participants will be instructed to say "stop" when the pressure sensation becomes painful.The average of 3 assessments on the tibialis anterior of the dominant side will be performed for analysis. The algometer pressure for assessment will be gradually increased at a rate of 1kg/second. Data will be collected in kg/cm2. At baseline and immediately after the conditioning stimulus
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