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Muscle Synergies in Pain and Pain Anticipation

Test-retest Fidelity of a Tool for Calculation of Muscle Synergies

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07251387
Enrollment
12
Registered
2025-11-26
Start date
2026-01-01
Completion date
2027-10-01
Last updated
2026-06-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nocebo Effect, Pain, Pain Anticipation

Keywords

Nocebo effect, Pain anticipation, Pain, Gait, Motricity, Muscle synergies

Brief summary

This study investigates how the anticipation of pain affects muscle synergies. One group will be recruited who will first experience actual pain from capsaicin cream and are then presented with a harmless cream deceptively labeled as capsaicin. The changes in muscle synergies will be measured during walking tasks.

Detailed description

Participants will be recruited through university announcements. Eligibility will be determined by a screening process that assesses prior experience with capsaicin cream. Healthy adults aged 18-35 who meet the inclusion criteria will be enrolled and assigned to experimental Group ("Prior Experience"): Individuals who report a prior painful experience with capsaicin cream. Participants will complete a first session consisting on a walking assessment on a treadmill. The speed will be incrementally increased from 0.8 m/s to 1.1 m/s. Throughout this task, muscle activity will be recorded via electromyography (EMG), and ground reaction forces will be captured by force platforms embedded in the treadmill. Following the initial walk, participants will complete a set of standardized questionnaires to establish baseline scores for pain perception (Visual Analog Scale, VAS), fear of movement (Tampa Scale of Kinesiophobia, TSK), and pain catastrophizing (Pain Catastrophizing Scale, PCS). Then, a capsaicin cream will be applied to the knee, specifically in the area between the lateral epicondyles of the femur, in a 4 cm wide band. Participants will immediately fill out the VAS to report any pain sensations. The walking assessment is repeated, measuring the same physiological signals (EMG and ground reaction forces). The participants will come to the laboratory a second time to measure the same outcomes but, instead of applying capsaicin again, they will receive an inert cream presented as capsaicin (neutral massage cream MEDICAFARM). The procedure will be repeated. The primary objective is to determine whether a prior painful experience with capsaicin causes individuals to generalize that pain memory to a neutral sensation, leading to different outcomes than in those who only have a negative expectation. We will specifically investigate the magnitude of this effect on muscle synergies.

Interventions

Participants receive a neutral cream with no real harmful effects with verbal and behavioral suggestions that it may cause localized pain. Researchers wear gloves during application and emphasize the potential discomfort, stating effects may intensify with movement.

OTHERGait assesment

Gait will be assessed both before and after cream application. Each assessment will consist of walking on a treadmill at varying speeds while physiological data (EMG) is recorded. Identical questionnaires (VAS, TAMPA, and PCS) will be administered immediately following the first gait assessment.

Sponsors

Universite de Picardie Jules Verne
Lead SponsorOTHER
Mitacs
CollaboratorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
BASIC_SCIENCE
Masking
NONE

Masking description

Participants are not aware that a cream applied to them (neutral cream) does not produce any pain.

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Aged 18-35 years old * Healthy participant with no self-reported diagnosed neurological, musculoskeletal, or cardiovascular disorders * Body Mass Index (BMI) \< 30 * Ability to walk unaided for at least 10 minutes without major physical limitations

Exclusion criteria

* Presence of pain at the time of testing * Self-reported diagnosed condition affecting mobility * Known allergy to any component of the study cream * Allergy to EMG electrode adhesives * Inability to stand unassisted for more than 1 minute * Inability to walk/run at the required speed and distance * Weight exceeding 150 kg (due to treadmill limitations) * Recent intake (prior intervention) of: * Analgesics (within 6 hours) * Cigarettes (within 6 hours) * Caffeine (within 2 hours) * Skin lesions at the cream application site * Pregnancy * Failure to understand instructions * Daytime pain reported by participant on day of experimentation

Design outcomes

Primary

MeasureTime frameDescription
Distribution of muscle synergies derived by non-negative matrix factorizationBefore intervention, after intervention (10 minutes after cream application)Changes in the activation of the muscle synergies during the gait cycle.
Changes in Muscle Synergy Composition derived by non-negative matrix factorization.Before intervention, after intervention (10 minutes after cream application)Changes in the composition of muscle synergies (i.e., the individuals muscles that comform one muscle synergy)

Secondary

MeasureTime frameDescription
Tampa Scale for Kinesiophobia (TSK)Before intervention.Tampa Scale of Kinesiophobia total score (17-68). Users rate 17 statements in a scale from 1 (Strongly disagree) to 4 (Strongly agree).

Countries

Canada, France

Contacts

CONTACTJennifer Burgos-Tirado, M.Sc.A., Ing.
jennifer.burgos.tirado@u-picardie.fr+33 7 71 27 11 35
STUDY_DIRECTORThierry Lelard, PhD, HDR

Lecturer

STUDY_DIRECTORMaryne Cozette, PhD, Lecturer

Lecturer

STUDY_DIRECTORGuillaume Léonard, PhD, Lecturer

Lecturer

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 12, 2026