KREHA: Strength Training With Eccentric Arm-cranking

Sponsor
Swiss Paraplegic Centre Nottwil (Other)
Overall Status
Completed
CT.gov ID
NCT05156411
Collaborator
(none)
14
1
1
8
1.8

Study Details

Study Description

Brief Summary

The new training device, the eccentric arm-crank, will be examined for its training effect by this project. That the training device can be used in athletes and patients with paraplegia in the future, the so-called "testing of the applicability of this concept" will be carried out during this study. Fourteen volunteer, healthy and trained people are first tested for their upper body performance, followed by a training phase over 20 trainings and at the and the performance data is collected again. The training intensity and duration is continuously increased during the training phase.

Condition or Disease Intervention/Treatment Phase
  • Other: eccentric arm-cranking training
N/A

Detailed Description

At the beginning, the study design includes an familiarisation appointment with performance tests and training on the eccentric arm-crank device (KREHA). At least one week later, the first test sequence including a maximum strength test (bench press), magnetic resonance imaging (MRI) to determine the muscle cross-section area of the upper arm and a test to determine the anaerobic performance (Wingate test) is conducted. The second test sequence takes place one to three days later. This includes a handgrip strength test, an aerobic endurance test (ramp test on the arm crank ergometer with ergospirometry) and a further familiarisation training on the KREHA. The training phase starts within two weeks after the pre-tests have been completed. There are two to a maximum of three trainings per week. These take 30 to 60 minutes and take place on the KREHA device under the supervision of the study staff. The training phase lasts a maximum of twelve weeks (20 training sessions). The first test sequence is repeated five to eight days after the last workout. The second test sequence takes place at the same time interval as in the pre-tests.

Study Design

Study Type:
Interventional
Actual Enrollment :
14 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Strength Training With Eccentric Arm-cranking
Actual Study Start Date :
Jul 1, 2021
Actual Primary Completion Date :
Feb 15, 2022
Actual Study Completion Date :
Mar 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Eccentric Training

This Group will train on the KREHA for 20 Trainings

Other: eccentric arm-cranking training
Over the twenty training sessions, able-bodied participants will exercise on the KREHA device. An arm-crank has to be decelerated, which will be rotated by a prematurely defined revolution rate and training duration. During this intervention a certain power has to be applied. During the whole time of training a continous progression in power and training duration is applied

Outcome Measures

Primary Outcome Measures

  1. Upper body Performance [through study completion, an average of 20 weeks]

    Peak Power - maximal reached power, generated during the 30sec Wingate arm-crank test

Secondary Outcome Measures

  1. Endurance Oxygen consumption [through study completion, an average of 20 weeks]

    VO2peak [ml/min/kg] - Basic Endurance test (Ergospirometry, arm-crank)

  2. Endurance Power [through study completion, an average of 20 weeks]

    Wmax [W] - Basic Endurance test (Ergospirometry, arm-crank)

  3. Upper body Mean Power [through study completion, an average of 20 weeks]

    Mean Power [W] - Wingate Test (arm-crank)

  4. Upper body Power - Time to Peak [through study completion, an average of 20 weeks]

    Time to Peak [s] - Wingate Test (arm-crank)

  5. Upper body Fatigue resistance [through study completion, an average of 20 weeks]

    Fatigue Index [%]- Wingate Test (arm-crank)

  6. Upper body Fatigue resistance [through study completion, an average of 20 weeks]

    Fatigue Slope [W/s] - Wingate Test (arm-crank)

  7. 1RM bench press [through study completion, an average of 20 weeks]

    One Repetition Maximum (1RM) [kg]- bench press

  8. Grip Strength [through study completion, an average of 20 weeks]

    Maximal Force that can be generated by pressing hand towards a fist [N]

  9. Cross sectional muscle area [through study completion, an average of 20 weeks]

    Cross sectional area of the upper arm is measured with MRI

  10. Upper Arm Circumference [through study completion, an average of 20 weeks]

    Circumference of the upper arm is measured with measuring tape

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • male or female

  • age between 18 and 50 years

  • experience in strength training

  • trained (minimum two times a week)

  • healthy

  • adequately informed and confirmed per signature

Exclusion Criteria:
  • findings during anamnesis of study doctor

  • pregnancy

Contacts and Locations

Locations

Site City State Country Postal Code
1 Swiss Paraplegic Centre Nottwil Lucerne Switzerland 6207

Sponsors and Collaborators

  • Swiss Paraplegic Centre Nottwil

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Swiss Paraplegic Centre Nottwil
ClinicalTrials.gov Identifier:
NCT05156411
Other Study ID Numbers:
  • 2020-26
First Posted:
Dec 14, 2021
Last Update Posted:
Aug 24, 2022
Last Verified:
Nov 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Swiss Paraplegic Centre Nottwil

Study Results

No Results Posted as of Aug 24, 2022