- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03332446
Influence of Cooling on the Effect of Strength Training (IceAge)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Recovery strategies represent a not sufficiently investigated chance in elite training control to optimize the complete training process. Coaches and athletes are confronted with numerous potentially effective recovery methods, e.g. cooling, warming, active recovery, compression, massage or power naps. However, the effectivity of these methods has rarely been investigated under controlled scientific conditions. Based on the state of the art,so far hardly any definite practical conclusions regarding effective recovery methods can be drawn, especially regarding sport-specific strategies and settings. Currently, cold water immersion is a particularly popular recovery strategy. However, there are hints that repeated cooling interventions after training can impair the training effect. This could potentially be caused by a faster reconstitution of homeostasis due to cooling. For fast recovery of performance, this effect would be desirable, but at the same time these homeostatic disturbances are the basis of signal processes leading to training adaptations.
The aim of this study is to investigate if regular cold water immersion after strength training has a negative influence on the desired training-induced performance enhancement.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Saarland
-
Saarbrücken, Saarland, Germany, 66123
- Saarland University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- healthy, 18-40 years, strength training experience, 8 weeks no leg strength training
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Crossover Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: cooling
strength training and cold water immersion
|
10 min at 12-15°C
|
No Intervention: control
strength training and no cold water immersion
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
1 Repetition Maximum
Time Frame: 8 weeks
|
Maximum weight in kg that can be successfully moved in a leg press
|
8 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Counter Movement Jump
Time Frame: 8 weeks
|
Maximum jump height in cm in a counter movement jump, measured with a force plate
|
8 weeks
|
blood parameters
Time Frame: 8 weeks
|
CRP, CK, IL-6, IGF-1
|
8 weeks
|
muscle biopsy
Time Frame: 8 weeks
|
p70S6, PAX7+, NCAM+
|
8 weeks
|
muscle thickness
Time Frame: 8 weeks
|
upper leg circumference in cm
|
8 weeks
|
subjective restfulness of sleep
Time Frame: 2 weeks
|
5-point Likert scale on subjective restfulness of sleep (1: very, 5: not at all)
|
2 weeks
|
time in bed
Time Frame: 2 weeks
|
Questionnaire recording time of going to bed (time in hh:mm), sleep onset latency (duration in min), waking time (time in hh:mm), and time of getting up (time in hh:mm).
From these items, the average time in bed per day is calculated, starting at "time of going to bed" and ending at "time of getting up".
|
2 weeks
|
sleeping time
Time Frame: 2 weeks
|
Questionnaire recording time of going to bed (time in hh:mm), sleep onset latency (duration in min), waking time (time in hh:mm), and time of getting up (time in hh:mm).
From these items, the average sleeping time per day is calculated, starting at "time of going to bed + sleep onset latency" and ending at "waking time".
|
2 weeks
|
questionnaire on recovery and stress
Time Frame: 2 weeks
|
Short Recovery and Stress Scale for Sport (SRSS): assessing recovery (physical performance capability, mental performance capability, emotional balance, overall recovery) and stress (muscular stress, lack of activation, negative emotional state, overall stress), each item is rated on a 7-point rating scale (0: does not apply at all, 6: fully applies).
For evaluation, two outcome values ("recovery" and "stress") are calculated as the sum of the corresponding subvalues, i.e. each outcome value is on a 25-point scale (0: does not apply at all, 24: fully applies).
|
2 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Tim Meyer, Prof., Universität des Saarlandes
Study record dates
Study Major Dates
Study Start
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 (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2512BI1901
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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