Feasibility Study of a Neuromuscular Fatigue Test and Associated Hemodynamic Responses: Application in Healthy Volunteers for Use in Patients with Chemotherapy-treated Breast Cancer (PROTECT-08A)

Institut de cancérologie Strasbourg Europe

Status: Completed

Conditions: Heart; Muscle; Fatigue

Treatments: Other: Test of neuromuscular fatigue and associated hemodynamic responses

Study type: Interventional

Funder types: Other

Identifiers

NCT06775119

2024-002

Details and patient eligibility

About

This cross-sectional and single-center study aims to progressively induce an increase in peripheral fatigue during successive efforts in healthy subjects. Participants will undergo three evaluations, each lasting one and half hours, to validate the test and assess its reproducibility. These three visits will be conducted at a minimum interval of 48 hours.

Enrollment: 30 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Man or woman
• Informed consent
• Age ≥ 18 years old
• Affiliation to a social security system
• Able to speak, read and understand French
• Practice physical activity 1 to 5 times per week, without reaching a level of intense training or high-level performance.

Exclusion criteria

• History of cancer
• Any known chronic pathology
• Protected minor or adult
• Psychiatric, musculoskeletal or neurological problems
• Implantation of a pacemaker
• Pregnant woman
• Presenting at least one contraindication to the use of transient blood flow occlusion

Trial design

Primary purpose: Prevention

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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30 participants in 1 patient group

Experimental protocol

Experimental group

Treatment:

Other: Test of neuromuscular fatigue and associated hemodynamic responses