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

July 20, 2026 updated by: Prof. Dr. Henning Wackerhage, Technical University of Munich

HyperLa: Glycolytic Phenotype (vLapeak) and Magnitude of Skeletal Muscle Hypertrophy After Resistance Training: A Multi-centre Study by the HyperLa Study Group

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.

Study Overview

Detailed Description

This multicentre, prospective, single-arm interventional cohort study aims to link metabolic phenotypes with physical adaptations.

  • Primary Assessment: Glycolytic power is quantified via the vLapeak test, defined as the peak rate of blood lactate accumulation during a 10-second isokinetic or sprint-configured cycle ergometry test.
  • Intervention: The 8-week resistance training program consists of two supervised sessions per week. Exercises include the leg press (or Smith-machine squat) and leg extensions, performed for 4 sets of 8-12 repetitions. Intensity progresses from an RPE of 6 to voluntary muscular failure by the third week.
  • Measurements: Muscle hypertrophy is primarily assessed via ultrasound measurement of muscle thickness and cross-sectional area (CSA) of the thigh muscles before and after the intervention.
  • Secondary Objectives: The study also evaluates changes in the plasma metabolome via venous blood samples and, at select sites, analyzes muscle biopsies for glycolytic enzyme activity and fiber type composition to further validate the vLapeak results.

Study Type

Interventional

Enrollment (Estimated)

120

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 Contact

Study Contact Backup

Study Locations

    • Central Finland
      • Jyväskylä, Central Finland, Finland, 40014
        • Recruiting
        • University of Jyväskylä, Faculty of Sport and Health Sciences
        • Contact:
    • Bavaria
      • München, Bavaria, Germany, 80809
        • Recruiting
        • Technical University of Munich, TUM School of Medicine and Health
        • Contact:
        • Contact:
    • North Rhine-Westphalia
      • Cologne, North Rhine-Westphalia, Germany, 51147
        • Recruiting
        • DLR Cologne, Department of Metabolism and Human Performance
        • Contact:
      • Düsseldorf, North Rhine-Westphalia, Germany, 40233
    • Saxony
      • Chemnitz, Saxony, Germany, 09126
        • Recruiting
        • TU Chemnitz, Sports Medicine and Exercise Therapy
        • Contact:
      • Leipzig, Saxony, Germany, 04109
        • Recruiting
        • Institute for Applied Training Science (IAT) Leipzig
        • Contact:
    • Limerick
      • Limerick, Limerick, Ireland, V94 T9PX
        • Recruiting
        • University of Limerick, Department of Physical Education and Sport Sciences (PESS)
        • Contact:
    • Madrid
      • Madrid, Madrid, Spain, 28040
        • Recruiting
        • Universidad Politécnica de Madrid, Facultad de Ciencias de la Actividad Física y del Deporte (INEF)
        • Contact:

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

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Body Mass Index (BMI) between 20-29 kg/m2
  • No structured resistance training performed in the last twelve months.
  • Maximum of four sessions per week of recreational or low-to-moderate aerobic endurance activity.
  • No history of competitive strength or physique sports.

Exclusion Criteria:

  • Diagnosed cardiovascular, pulmonary, metabolic, neuromuscular, or orthopaedic disease that contraindicates exercise.
  • Positive response to any question on the PAR-Q 2025 questionnaire.
  • Current use of anabolic steroids, creatine, or other substances known to strongly influence muscle hypertrophy.
  • Regular engagement in shift work.
  • Women who are pregnant or breastfeeding.

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: Treatment
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Resistance Training Group
Participants in this single-arm cohort will undergo an 8-week standardized, hypertrophy-focused lower-body resistance training program.
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.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in mid-thigh Muscle Thickness
Time Frame: Baseline and Week 8 (completion of training intervention)
Change in mid-thigh muscle thickness (combination of rectus femoris and vastus intermedius) as measured by ultrasound.
Baseline and Week 8 (completion of training intervention)
Change in lateral-thigh Muscle Thickness
Time Frame: Baseline and Week 8 (completion of training intervention)
Change in lateral thigh muscle thickness (combination of vastus lateralis and vastus intermedius) as measured by ultrasound.
Baseline and Week 8 (completion of training intervention)

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in Peak Rate of Blood Lactate Accumulation (vLapeak)
Time Frame: Baseline and Week 8 (completion of training intervention)
Peak rate of blood lactate accumulation before and after a 10-second all-out seated cycle ergometry test. Blood lactate will be sampled every minute for 10 minutes post-test to capture the peak value.
Baseline and Week 8 (completion of training intervention)
Change in Vastus Lateralis Muscle Cross-Sectional Area (CSA)
Time Frame: Baseline and Week 8 (completion of training intervention)
Change in cross-sectional area of the vastus lateralis at 50% of muscle length measured via ultrasound.
Baseline and Week 8 (completion of training intervention)
Maximal Strength (3RM) for Leg Press
Time Frame: Baseline and Week 8 (completion of training intervention)
Change in 3-Repetition Maximum (3RM) for the leg press exercise to assess lower-body multi-joint maximal strength.
Baseline and Week 8 (completion of training intervention)
Maximal Strength (3RM) for Leg Exentsion
Time Frame: Baseline and Week 8 (completion of training intervention)
Change in 3-Repetition Maximum (3RM) for the leg extension exercise to assess single-joint quadriceps strength.
Baseline and Week 8 (completion of training intervention)
Change in Relative Abundance of Selected Plasma Metabolites
Time Frame: Baseline and Week 8 (completion of training intervention)
Change in the relative concentration of targeted plasma metabolites from baseline to Week 8, as analyzed via mass spectrometry.
Baseline and Week 8 (completion of training intervention)

Collaborators and Investigators

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

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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 (Actual)

May 4, 2026

Primary Completion (Estimated)

December 1, 2026

Study Completion (Estimated)

December 1, 2026

Study Registration Dates

First Submitted

June 25, 2026

First Submitted That Met QC Criteria

July 20, 2026

First Posted (Actual)

July 23, 2026

Study Record Updates

Last Update Posted (Actual)

July 23, 2026

Last Update Submitted That Met QC Criteria

July 20, 2026

Last Verified

June 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

IPD Plan Description

A formal plan for sharing individual participant data (IPD) with external researchers has not yet been finalized. The study involves a multicentric international consortium with strict data protection requirements under GDPR. Data is currently managed centrally via REDCap at the Technical University of Munich. Requests for data sharing will be considered on a case-by-case basis by the HyperLa Study Group after the primary publication of results, and would require a formal proposal and a signed Data Access or Material Transfer Agreement (MTA)

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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