Clinical Trials in Spain / NCT07427979
Starting soon Not applicable

Sex Differences in Exercise-Induced Hypoalgesia

NCT07427979 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2026-03-15
Last updated
2026-03-18

Condition(s) studied

Healthy Adult

Investigational drug(s) / intervention(s)

Aerobic exercise using cycle ergometer

Aerobic exercise using cycle ergometer: Participants will perform a 30-minute aerobic exercise protocol using a lower-limb cycle ergometer at 70% heart rate reserve. The protocol includes: * 5-minute warm-up * 20-minute exercise at target intensity * 5-minute cool-down Heart rate will be monitored continuously using a validated heart rate monitor.

Study summary

Exercise-induced hypoalgesia (EIH) refers to the reduction in pain sensitivity following acute exercise. Although aerobic exercise has been shown to induce hypoalgesia in healthy individuals, it remains unclear whether the magnitude of this response differs between men and women.

This quasi-experimental study aims to evaluate sex differences in pressure pain thresholds following a standardized aerobic exercise protocol using a lower-limb cycle ergometer. Pressure pain thresholds will be assessed before exercise, immediately after exercise, and 30 minutes after exercise in healthy adults aged 18 to 65 years.

The findings of this study may contribute to improving individualized exercise prescription strategies based on sex differences in pain modulation.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy male and female adults * Age between 18 and 65 years * Able to perform moderate-to-vigorous aerobic exercise * Able to understand study procedures * Cleared for exercise participation using the Physical Activity Readiness Questionnaire (PAR-Q). Exclusion Criteria: * Cardiovascular, respiratory, neurological, or metabolic diseases contraindicating exercise * Current musculoskeletal pain or injury * Analgesic medication use within 24 hours prior to testing * Vigorous exercise within 24 hours prior to testing * Any contraindication to aerobic exercise

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Centro Superior de Estudios Universitarios La Salle Madrid Madrid

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Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07427979 on ClinicalTrials.gov ↗ ← All trials in Spain