Krafttraining mit exzentrischem Armkurbeln bei Para-Athleten (KREHA-ParAth)
The new training device, the eccentric arm-crank, will be examined for its training effects in athletes with a spinal cord injury (SCI) by this project. That the training device can be used in 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 athletes with SCI are first tested for their upper body performance, followed by a training phase over 20 trainings and at the end the performance data is collected again. The training intensity and duration is continuously increased during the training phase.
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
At the beginning, the study design includes a 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) 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 45 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.
Studientyp
Einschreibung (Tatsächlich)
Phase
- Unzutreffend
Kontakte und Standorte
Studienorte
-
-
Canton of Lucerne
-
Nottwil, Canton of Lucerne, Schweiz, 6207
- Swiss Paraplegic Centre
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- male or female with traumatic or disease-related SCI
- age between 18 and 50 years
- experience in strength training
- Squad status or at least 4h per week training
- Biceps/triceps function
- healthy(study physician)
- adequately informed and confirmed per signature
Exclusion Criteria:
- findings during anamnesis of study physician
- pregnancy
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Grundlegende Wissenschaft
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: Eccentric Training
This Group will train on the KREHA for 20 Trainings |
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. |
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Upper body Performance
Zeitfenster: through study completion, an average of 20 weeks
|
Peak Power - maximal reached power, generated during the 30sec Wingate arm-crank test |
through study completion, an average of 20 weeks
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Endurance Oxygen consumption
Zeitfenster: through study completion, an average of 20 weeks
|
VO2peak [ml/min/kg] - Basic Endurance test (Ergospirometry, arm-crank) |
through study completion, an average of 20 weeks
|
|
Maximal Workload
Zeitfenster: through study completion, an average of 20 weeks
|
Wmax [W] - Basic Endurance test (Ergospirometry, arm-crank) |
through study completion, an average of 20 weeks
|
|
Upper body Mean Power
Zeitfenster: through study completion, an average of 20 weeks
|
Mean Power [W] - Wingate Test (arm-crank) |
through study completion, an average of 20 weeks
|
|
Upper body Power - Time to Peak
Zeitfenster: through study completion, an average of 20 weeks
|
Time to Peak [s] - Wingate Test (arm-crank) |
through study completion, an average of 20 weeks
|
|
Upper body Fatigue Index
Zeitfenster: through study completion, an average of 20 weeks
|
Fatigue Index [%]- Wingate Test (arm-crank) |
through study completion, an average of 20 weeks
|
|
Upper body Fatigue Slope
Zeitfenster: through study completion, an average of 20 weeks
|
Fatigue Slope [W/s] - Wingate Test (arm-crank) |
through study completion, an average of 20 weeks
|
|
1RM bench press
Zeitfenster: through study completion, an average of 20 weeks
|
One Repetition Maximum (1RM) [kg]- bench press |
through study completion, an average of 20 weeks
|
|
Grip Strength
Zeitfenster: through study completion, an average of 20 weeks
|
Maximal Force that can be generated by pressing hand towards a fist [N] |
through study completion, an average of 20 weeks
|
|
Upper Arm Circumference
Zeitfenster: through study completion, an average of 20 weeks
|
Circumference of the upper arm is measured with measuring tape |
through study completion, an average of 20 weeks
|
|
Lower Arm Circumference
Zeitfenster: through study completion, an average of 20 weeks
|
Circumference of the lower arm is measured with measuring tape |
through study completion, an average of 20 weeks
|
Mitarbeiter und Ermittler
Ermittler
- Hauptermittler: Fabian Ammann, MSc, SPZ
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Tatsächlich)
Studienabschluss (Tatsächlich)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 2022-06
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .