- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04541901
Massage and Cold Water Immersion on Movement Variability After Fatigue in Swimmers
Effects of Post Exercise Massage and Cold-water Immersion on Movement Variability After Fatigue in Swimmers: a Randomized Controlled Clinical Trial
The goal of this clinical trial is to investigate the effectiveness of post-exercise massage and cold-water immersion compared to control in young elite swimmers. The main questions it aims to answer are:
- Is post-exercise techniques effective for recovery of the movement variability, , myotonometric, ergometric and perceptive parameters after fatigue?
- Can neuromuscular fatigue protocols impair movement variability, myotonometric, ergometric and perceptive parameters?
- What tests are reliable to assess different aspects of swimmers' recovery?
Researchers will compare massage and cold-water immersion to control and to each other to see if recovery is antecipated. They will also compare an in-water and an out-of-water fatigue protocol to see if they are effective and can be used in different settings.
Participants will:
- Perform test and retest sessions to assess movement variability, myotonometric, ergometric and perceptive parameters.
- Perform an in-water fatigue protocol consisting of 8x100m front-crawl sprints
- Receive three recovery strategies in a randomized order (massage, cold-water immersion and control (i.e. rest)
- Answer a questionnaire regarding ther beliefs and preferences for recovery.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
São Paulo
-
Presidente Prudente, São Paulo, Brazil, 19060-900
- Faculty of Science and Technology (UNESP)
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- male and female athletes
- between 15 and 30 years old
- no injury over the last month (any complaint that prevented the athlete from training or compete at least once)
Exclusion Criteria:
- use of pain killers at least 24h before study participation
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Massage
12 minutes of effleurage and petrissage on the upper limbs administered after fatiguing exercise in the swimming pool
|
12 minutes of effleurage and petrissage on the upper limbs
|
|
Experimental: Cold-water immersion
12 minutes of cold-water immersion at the shoulder level with water temperature between 11 to 15°C
|
12 minutes of cold water immersion at the shoulder level with water temperature between 11 to 15°C
|
|
No Intervention: Control
12 minutes of rest.
The athletes are free to sit or walk around the place but are advised to refrain from exercise in and out of the pool.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Movement variability
Time Frame: From enrollment to the end of crossover treatments at 6 weeks
|
Obtained from time series of biomechanical data expressed as degrees of shoulder and elbow flexion, and ergometric variables (i.e. pace, stroke frequency and average power) executed during a simulated out of water swim ergometric test to understand the impacts of fatigue on movement and explore changes during recovery. Measured at baseline, post-fatigue and post-interventions. Joint angles time series of shoulder and elbow flexion and ergometric variables were aggregated using mean, standard deviation and variation coefficients for data analyses. |
From enrollment to the end of crossover treatments at 6 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Swim-related perceptions
Time Frame: From enrollment to the end of crossover treatments at 6 weeks
|
Self-reported ratings regarding physical and mental readiness for exercise, fatigue, vigor, somnolence, pain, and perception of effort and recovery, measured by a numerical rating scale ranging from 0 (nothing) to 10 (extreme).
Measured at baseline, post-fatigue and post-interventions
|
From enrollment to the end of crossover treatments at 6 weeks
|
|
Myotonometry
Time Frame: From enrollment to the end of crossover treatments at 6 weeks
|
Muscle tone, stiffness and elasticity were assessed by the MyotonPRO.
The equipment probe will be placed perpendicular to the skin surface on the muscle belly previously marked with a pen by the evaluator at 1: Deltoid; 2: Pectoralis Major; 3: Biceps brachii; 4: Upper Trapezius; 5: Latissimus dorsi; 7: Triceps.
Values were deemed acceptable if there were less than 3% of variation between the impulses.
Measured at baseline, post-fatigue and post-interventions.
|
From enrollment to the end of crossover treatments at 6 weeks
|
|
Skin temperature
Time Frame: From week 4 to 6
|
The temperature will be measured using an infrared thermographic camera, at the same points of myotonometry.
Measured before and after the interventions.
|
From week 4 to 6
|
|
Beliefs in the recovery techniques
Time Frame: Week 6
|
Participants will be asked if they believe that massage, cold-water immersion and resting contribute to their recovery before and after the study
|
Week 6
|
|
Preference
Time Frame: Week 6
|
After the study the participants will be asked which of the interventions they preferred to received to recover from the fatiguing exercise
|
Week 6
|
|
Sense of position
Time Frame: From enrollment to the end of crossover treatments at 6 weeks
|
Participants will be asked to position their dominant upper limb at 90° which will be indicated by a target fixed on the wall 1 meter ahead of them.
They will have 3 chances to point at the target and memorize the position.
Afterwards, participants will have 3 chances to point at the target without vision (by blindfold).
Measured at baseline, post-fatigue and post-interventions
|
From enrollment to the end of crossover treatments at 6 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Study Director: Carlos M Pastre, Doctor, University of São Paulo State, UNESP
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- ECD001
- 001 (Buy Pharma Ecza Deposu San. Tic. Ltd.)
- 2020/11146-0 (Other Grant/Funding Number: São Paulo Research Foundation)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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