MedPath

Investigating the Effects of Different Soft Tissue Mobilizations on Delayed Onset Muscle Soreness

Not Applicable
Completed
Conditions
Muscle Soreness
Registration Number
NCT04248764
Lead Sponsor
Izmir Katip Celebi University
Brief Summary

Delayed onset muscle soreness (DOMS) is associated with the initiation of a new physical activity or a sudden increase in exercise volume and intensity. DOMS also occurs following eccentric exercises such as ballistic stretching, downhill running, weight training and plyometrics. DOMS might prevent performing sports and decreases the performance of professional or recreational athletes. Recently, different soft tissue mobilization applications (massage, foam roller) have been preferred by many athletes to prevent DOMS. However, there is no study comparing the effects of these techniques on DOMS. Therefore, the aim of the present study is to investigate the effects of different soft tissue mobilization practices on DOMS and sportive performance in recreational athletes. In order to achieve this goal, a total of 36 recreational athletes will be included and will be allocated to three groups as foam roller group (n=12), massage group (n=12) and control group (n=12). Demographic data, thermal camera measurements, fatigue level assessments, and performance measurements will be performed. All measurements will be carried out four times as before the application, immediately after the application, after 24 hours and after 48 hours.

Detailed Description

After being invited to the study, the demographic data of all participants who agreed to participate in the study will be recorded on a structured form. Participants will be randomly divided into three groups: Massage application group, Foam Roller application group and Control group. Afterwards, thermal imaging, perceived fatigue and pain level, blood lactate level measurements, and vertical jump assessments will be done for the quadriceps femoris muscle. Then, the fatigue protocol will be applied for the quadriceps femoris muscle and five-minute applications will be made according to the groups in which they are randomly separated. Evaluations made in the first applications will be made immediately after the applications, 24 hours and 48 hours later, as the 2nd, 3rd and 4th measurements. The assessor will not know which group the participants are from.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
36
Inclusion Criteria
  • Performing recreational sports at least 1 and at most 3 times a week.
Exclusion Criteria
  • Any musculoskeletal, neurological or other serious health problems experienced in the past six months
  • Not willing to participate in the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Tissue Temperature ChangeFour measurements will be performed as immediately before, immediately after, 24 hours and 48 hours later from fatigue protocol.

Tissue temperature change will be assessed by using thermal camera imaging which is a non-invasive method. By determining the temperature differences in the tissues with the thermal camera, it will be determined in which regions the circulation increases or decreases.

Blood Lactate Level ChangeFour measurements will be performed as immediately before, immediately after, 24 hours and 48 hours later from fatigue protocol.

Lactate Edge will be used and the lactate levels will be measured from a drop of blood.

Secondary Outcome Measures
NameTimeMethod
Change in Lower Extremity Anaerobic PerformanceFour measurements will be performed as immediately before, immediately after, 24 hours and 48 hours later from fatigue protocol.

Vertical jump test will be used to evaluate the lower extremity anaerobic performance.

Perceived Fatigue and Pain Level ChangesFour measurements will be performed as immediately before, immediately after, 24 hours and 48 hours later from fatigue protocol.

By using a 0-100 millimeter visual analog scale (0: none, 100: maximum), the participants will determine the fatigue and pain levels. Higher scores indicate worse fatigue and pain.

Trial Locations

Locations (1)

Izmir Katip Celebi University

🇹🇷

İzmir, Turkey

Izmir Katip Celebi University
🇹🇷İzmir, Turkey
© Copyright 2025. All Rights Reserved by MedPath