Effectiveness of Pulsed Electromagnetic Field Therapy as an Adjunct Modality to Warm-up Exercise: a Randomized Controlled Trial
Pulsed electromagnetic field therapy
+ Sham treatment
Prevention Study
Summary
Study start date: August 30, 2022
Actual date on which the first participant was enrolled.This clinical trial is designed to evaluate whether pulsed electromagnetic field therapy (PEMF) can enhance the benefits of warm-up exercises in healthy individuals. The focus is on improving the range-of-motion in the knee and reducing muscle stiffness in the quadriceps, which are key factors in preventing sports injuries. By analyzing the immediate effects of a single PEMF session combined with a warm-up exercise, this study aims to uncover potential new methods for protecting against injuries during physical activities. Participants in the study undergo several measurements to assess their knee flexibility and muscle stiffness. Initially, these measurements are taken without any treatment. Then, participants receive a ten-minute PEMF treatment around their knee, followed by another set of measurements. After this, they engage in a five-minute warm-up session on a stationary bike, with a final round of measurements taken afterwards. The outcomes of the PEMF treatment are compared to a sham treatment to determine its effectiveness, using a special ultrasound technique called shear wave elastography to ensure accurate results.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.20 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Prevention 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 40 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
50% chance of being blinded to the placebo group
Treatment Groups
Group I
ExperimentalGroup II
ShamStudy 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
CUHK-ORT Sports Injury Research Laboratory
Hong Kong, Hong KongOpen CUHK-ORT Sports Injury Research Laboratory in Google Maps