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Pain-Related Fear and Motor Control in Healthy Volunteers
Sponsor: Universite de Picardie Jules Verne
Summary
The goal of this clinical trial is to learn how experimentally induced movement-related threat affects emotional, autonomic, and motor responses in healthy adults. The main questions it aims to answer are: * Does movement-related threat change walking performance or upper-limb pointing movements? * Are these effects moderated by participants' level of kinesiophobia? * Does movement-related threat increase apprehension or alter heart rate variability responses? Participants will complete two experimental conditions during one session: a control condition and an experimental condition. In both conditions, inactive transcutaneous electrical nerve stimulation (TENS) electrodes will be placed in the lumbar region. In the experimental condition, participants will receive verbal suggestions about discomfort, movement-evoked pain, and potential unpredictable electrical stimulation to create the threat of pain associated with movement. Participants will complete a baseline assessment of kinesiophobia, followed by walking and pointing tasks, while perceived apprehension and autonomic responses are assessed.
Official title: Understanding the Interaction Between Pain-Related Fear and Motor Control: Manipulating Movement-Related Threat in Healthy Volunteers
Key Details
Gender
All
Age Range
18 Years - 65 Years
Study Type
INTERVENTIONAL
Enrollment
26
Start Date
2025-11-03
Completion Date
2026-07-06
Last Updated
2026-07-08
Healthy Volunteers
Yes
Interventions
Movement-Related Threat Induction
Experimental induction of movement-related threat using verbal suggestions about potential discomfort and movement-evoked pain associated with electrodes placed in the lumbar region, as well as unpredictable electrical stimulation from an inactive transcutaneous electrical nerve stimulation device. The manipulation aimed to increase movement-related apprehension and anxiety during motor tasks.
Neutral Movement Condition
Control condition using verbal suggestions about the safety and reliability of electrodes placed in the lumbar region and associated with an inactive transcutaneous electrical nerve stimulation device. No threat-related information regarding discomfort, movement-evoked pain, or unpredictable electrical stimulation was provided. The condition aimed to assess motor and autonomic responses during motor tasks under neutral instructions.
Locations (1)
Eurasport
Loos, France