Influence of Cooling on the Effect of Strength Training (IceAge)

November 14, 2017 updated by: Anne Krieg M.D., Universität des Saarlandes
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 Overview

Status

Completed

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

Interventional

Enrollment (Actual)

11

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Saarland
      • Saarbrücken, Saarland, Germany, 66123
        • Saarland University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 40 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • healthy, 18-40 years, strength training experience, 8 weeks no leg strength training

Exclusion Criteria:

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Tim Meyer, Prof., Universität des Saarlandes

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

August 1, 2014

Primary Completion (Actual)

July 1, 2017

Study Completion (Actual)

July 1, 2017

Study Registration Dates

First Submitted

March 29, 2016

First Submitted That Met QC Criteria

November 1, 2017

First Posted (Actual)

November 6, 2017

Study Record Updates

Last Update Posted (Actual)

November 17, 2017

Last Update Submitted That Met QC Criteria

November 14, 2017

Last Verified

November 1, 2017

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)?

UNDECIDED

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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