Effects of Foam Rolling Versus Stretching Exercises on Quadriceps, Hamstrings and Calf Muscle Length in University Sport's Students
Foam rolling
+ Stretching exercises
Treatment Study
Summary
Study start date: August 30, 2021
Actual date on which the first participant was enrolled.The aim of the current study is to determine the effects of foam rolling versus stretching exercises on quadriceps, hamstrings and muscle length in university sport's students. It will be a Randomized control trial and will be conducted at University of Lahore. Purposive sampling technique will be used to collect data as per inclusion criteria the participant age between 18 to 25 years and male and female healthy participants. A history of cardiovascular or respiratory disease, any history of fractures or surgeries in the lower extremity in the past years will be excluded. Patients will be randomly allocated into two groups; Group A will be treated with the effects of foam rolling on quadriceps, hamstrings and calf muscles. 5 min cycle ergometry, 6 min foam rolling 3 times for 30sec. Group B will be treated with the effects of stretching exercise on quadriceps, hamstrings and calf muscles. 5 min cycle ergometry, 6 min stretching exercises 3 times for 30sec for three sessions of treatment per week will be given. In both group's pre and post-test measurements of quadriceps, hamstrings and calf muscle length will be assessed through goniometer and Lower Extremity Functional Scale (LEFS) will be assessed to measure initial functions of lower limb. Evaluation will be done before session start and at the end of week. Total session will be given for at least 2 months.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.50 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 25 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
Active ComparatorStudy Objectives
Primary 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