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
3 other identifiers
interventional
22
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2023
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 27, 2020
CompletedFirst Posted
Study publicly available on registry
September 9, 2020
CompletedStudy Start
First participant enrolled
March 6, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 30, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2023
CompletedNovember 5, 2024
November 1, 2024
7 months
August 27, 2020
November 4, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Movement variability
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 Outcomes (6)
Swim-related perceptions
From enrollment to the end of crossover treatments at 6 weeks
Myotonometry
From enrollment to the end of crossover treatments at 6 weeks
Skin temperature
From week 4 to 6
Beliefs in the recovery techniques
Week 6
Preference
Week 6
- +1 more secondary outcomes
Study Arms (3)
Massage
EXPERIMENTAL12 minutes of effleurage and petrissage on the upper limbs administered after fatiguing exercise in the swimming pool
Cold-water immersion
EXPERIMENTAL12 minutes of cold-water immersion at the shoulder level with water temperature between 11 to 15°C
Control
NO INTERVENTION12 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.
Interventions
12 minutes of cold water immersion at the shoulder level with water temperature between 11 to 15°C
Eligibility Criteria
You may qualify if:
- 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)
You may not qualify if:
- use of pain killers at least 24h before study participation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Flávia Carvalholead
- Universidade Estadual Paulista Júlio de Mesquita Filhocollaborator
- São Paulo State Universitycollaborator
Study Sites (1)
Faculty of Science and Technology (UNESP)
Presidente Prudente, São Paulo, 19060-900, Brazil
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Carlos M Pastre, Doctor
University of São Paulo State, UNESP
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- MSc
Study Record Dates
First Submitted
August 27, 2020
First Posted
September 9, 2020
Study Start
March 6, 2023
Primary Completion
September 30, 2023
Study Completion
September 30, 2023
Last Updated
November 5, 2024
Record last verified: 2024-11
Data Sharing
- IPD Sharing
- Will not share
The individual participant data will not be shared because they belong to a competitive team and most of the participants have less than 18 years old