- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT07612956
Effects of a 4-Week Altitude Training on Sport-Specific Performance, Body Composition, and Cardiac and Pulmonary Function in Adolescent Male Rowers
Effects of a 4-Week Altitude Training on Sport-Specific Performance, Body Composition, and Cardiac and Pulmonary Function in Adolescent Male Rowers: The Potential Role of Maturation
Studie Overzicht
Toestand
Interventie / Behandeling
Studietype
Inschrijving (Geschat)
Fase
- Niet toepasbaar
Contacten en locaties
Studiecontact
- Naam: Ziyue Ou
- Telefoonnummer: +853 8591 2000
- E-mail: research_ethics@ipm.edu.mo
Studie Locaties
-
-
Macao
-
Macao, Macao, China
- Werving
- Macao Polytechnic University, Faculty of Health Sciences and Sports
-
Contact:
- Chaoran Han
- Telefoonnummer: +853 8591 2000
- E-mail: hanchaoran1999@outlook.com
-
-
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Kind
- Volwassen
Accepteert gezonde vrijwilligers
Beschrijving
Inclusion Criteria:Male adolescent rowers aged 12-19 years Regularly training and participating in competitive rowing Willing to participate in 4-week altitude training program and follow testing protocol -
Exclusion Criteria:Any cardiovascular, respiratory, hematologic, or musculoskeletal disorders Injury or illness preventing participation in high-intensity rowing training Participation in another high-altitude training program within the last 3 months Any medical contraindication to blood sampling
-
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Ander
- Toewijzing: Niet-gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: Post-PHV group
Participants in the Post-PHV group are adolescent male rowers stratified by biological maturation (PHV offset).
They will undergo the same 4-week high-altitude training program, including aerobic, anaerobic, and sport-specific rowing exercises.
Pre- and post-training measurements of athletic performance, athletic body composition, athletic cardiac and pulmonary function, and hematological markers will be collected.
|
Participants undergo a 4-week altitude training program, including aerobic, anaerobic, and sport-specific rowing exercises.
Both Post-PHV and Mid-PHV groups receive the same training protocol.
Pre- and post-training assessments include athletic performance, athletic body composition, athletic cardiac and pulmonary function, and hematological markers.
Participants are stratified by biological maturation (PHV offset) to explore whether maturity influences training adaptations.
|
|
Experimenteel: Mid-PHV group
Participants in the Post-PHV group are adolescent male rowers stratified by biological maturation (PHV offset).
They will undergo the same 4-week high-altitude training program, including aerobic, anaerobic, and sport-specific rowing exercises.
Pre- and post-training measurements of athletic performance, athletic body composition, athletic cardiac and pulmonary function, and hematological markers will be collected.
|
Participants undergo a 4-week altitude training program, including aerobic, anaerobic, and sport-specific rowing exercises.
Both Post-PHV and Mid-PHV groups receive the same training protocol.
Pre- and post-training assessments include athletic performance, athletic body composition, athletic cardiac and pulmonary function, and hematological markers.
Participants are stratified by biological maturation (PHV offset) to explore whether maturity influences training adaptations.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Peak Power During Wingate Test
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
Peak power measured during the Wingate anaerobic test before and after the intervention.
|
Pre-training and immediately post 4-week altitude training
|
|
Maximal Oxygen Uptake
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
Pre- and post-intervention measurement of VO₂max using standard exercise testing protocol to assess aerobic capacity in adolescent male rowers.
|
Pre-training and immediately post 4-week altitude training
|
|
Mean Power Output During 1500 m Rowing Test
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
Mean power output measured during the 1500 m rowing ergometer test before and after the intervention.
|
Pre-training and immediately post 4-week altitude training
|
|
Body Weight
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
Body weight measured before and after the training period.
|
Pre-training and immediately post 4-week altitude training
|
|
Body Fat Percentage
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
Body fat percentage measured using bioelectrical impedance or other validated method.
|
Pre-training and immediately post 4-week altitude training
|
|
Forced Vital Capacity (FVC)
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
Forced vital capacity measured using spirometry before and after the intervention.
|
Pre-training and immediately post 4-week altitude training
|
|
Maximal Voluntary Ventilation
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
MVV measured using standard pulmonary function testing protocol pre- and post-intervention.
|
Pre-training and immediately post 4-week altitude training
|
|
Left Ventricular Volume
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
Echocardiography measurement of left ventricular end-diastolic and end-systolic volume.
|
Pre-training and immediately post 4-week altitude training
|
|
Ejection Fraction
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
Echocardiography assessment of left ventricular ejection fraction pre- and post-training.
|
Pre-training and immediately post 4-week altitude training
|
|
Myocardial Thickness
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
Measurement of interventricular septum and left ventricular posterior wall thickness by echocardiography.
|
Pre-training and immediately post 4-week altitude training
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Muscle Mass
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
Skeletal muscle mass measured pre- and post-training.
|
Pre-training and immediately post 4-week altitude training
|
|
Red Blood Cell Count
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
RBC count measured from venous blood samples pre- and post-intervention.
|
Pre-training and immediately post 4-week altitude training
|
|
Hemoglobin
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
Hemoglobin concentration measured from venous blood samples.
|
Pre-training and immediately post 4-week altitude training
|
|
Hematocrit
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
Hematocrit levels measured pre- and post-training.
|
Pre-training and immediately post 4-week altitude training
|
|
Erythropoietin
Tijdsspanne: Pre-training and immediately post 4-week altitude training
|
Plasma EPO concentration measured from venous blood samples.
|
Pre-training and immediately post 4-week altitude training
|
Medewerkers en onderzoekers
Sponsor
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Andere studie-ID-nummers
- FCSD/DPPESS-2026/003
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .