Glycolytic Phenotype (vLapeak) and Magnitude of Skeletal Muscle Hypertrophy After Resistance Training

NCT07721766 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2026-07-23

No results posted yet for this study

Summary

The HyperLa study investigates whether a person's "glycolyticness"-the efficiency with which their body uses glycolysis for energy-can predict how much their muscles will grow (hypertrophy) in response to resistance training. Participants will undergo a specialized "vLapeak" test, which measures the maximal rate of lactate accumulation during a 10-second all-out cycling sprint, to determine their individual glycolytic power. Following this initial assessment, participants will complete eight weeks of standardized, twice-weekly resistance training focused on the lower body. The study aims to determine if individuals with higher initial vLapeak values experience greater increases in muscle size compared to those with lower values. This research may help explain why people respond differently to exercise and support the development of personalized training programs.

Conditions

  • Healthy Volunteers
  • Muscle Hypertrophy
  • Glycolysis
  • Moderately Trainend

Interventions

BEHAVIORAL

Hypertrophy-focused Resistance Training

Standardized training consisting of twice-weekly supervised sessions for 8 weeks. Each session includes 4 sets of 8-12 repetitions of leg press (or Smith-machine squat) and leg extensions. Training intensity progresses from an RPE of 6 to voluntary muscular failure starting from week three.

Sponsors & Collaborators

  • Chemnitz University of Technology

    collaborator OTHER
  • DLR German Aerospace Center

    collaborator OTHER
  • University of Jyvaskyla

    collaborator OTHER
  • University of Limerick

    collaborator OTHER
  • IST University of Applied Sciences Düsseldorf

    collaborator UNKNOWN
  • Institute for Applied Training Science (IAT/FES e.V.)

    collaborator UNKNOWN
  • Technical University of Munich

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
39 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2026-05-04
Primary Completion
2026-12-01
Completion
2026-12-01

Countries

  • Finland
  • Germany
  • Ireland
  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07721766 on ClinicalTrials.gov