Exercise-Induced Hypoalgesia in Upper and Lower Limb Training
Lower limb resistance training
+ Upper limb resistance training
Treatment Study
Summary
Study start date: February 15, 2025
Actual date on which the first participant was enrolled.This study focuses on understanding how resistance training can affect pain perception in different parts of the body, specifically comparing exercise involving the arms versus the legs. Healthy participants are divided into three groups: one group performs resistance exercises with their legs, another uses their arms, and a third group does not do any specific exercises for comparison. The goal is to see if exercising specific parts of the body can reduce pain sensitivity, a phenomenon known as exercise-induced hypoalgesia, and to compare the effects between the trained limbs and other areas of the body. This research is important because it could help develop targeted exercise programs to manage pain more effectively. Participants in the study will perform specific resistance exercises such as biceps curls for the arms and leg extensions for the legs. Each exercise session consists of three sets of five repetitions. The study measures the effect of these exercises on pain perception by assessing the pressure pain thresholds in the participants' thighs and elbows. This means researchers will evaluate how much pressure a person can handle before feeling pain at these points, both where they exercised and in another area. By comparing these measurements across the different groups, the study aims to determine how different types of resistance training might influence pain sensitivity in various parts of the body.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.90 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 64 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location