NCT07245225

Brief Summary

The goal of this study is to investigate the acute effects of drop-landing exercise on the bone metabolism biomarkers and extracellular vesicles in healthy young males, in order to gain a deeper understanding of the mechanotransduction mechanisms involved in bone metabolism. The main question aims to answer: • Does a single bout acute drop-landing exercise change serum sclerostin, other bone signaling markers, and circulating extracellular vesicles levels? Participants complete both the drop-landing and control trials in a randomized order, with a minimum washout period of one week between trials. During each trial, blood samples are collected at three time points: pre-, immediately post, and 1-hour post drop-landing/control exercise.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
15

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jan 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 15, 2024

Completed
1.8 years until next milestone

First Submitted

Initial submission to the registry

November 14, 2025

Completed
10 days until next milestone

First Posted

Study publicly available on registry

November 24, 2025

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
Last Updated

November 24, 2025

Status Verified

November 1, 2025

Enrollment Period

2 years

First QC Date

November 14, 2025

Last Update Submit

November 20, 2025

Conditions

Keywords

ExerciseBone turnoverExtracellular vesiclesWnt/β-catenin signaling pathway

Outcome Measures

Primary Outcomes (1)

  • Serum sclerostin concentration

    Serum sclerostin concentration is quantified using an enzyme-linked immunosorbent assay (ELISA) and reported in picograms per milliliter (pg/mL).

    Blood samples are collected at pre- (baseline), immediately post, 1-hour post drop-landing/control exercise in main trials.

Secondary Outcomes (5)

  • Serum dickkopf Wnt signaling pathway inhibitor 1 (DKK1) concentration

    Blood samples are collected at pre- (baseline), immediately post, 1-hour post drop-landing/control exercise in main trials.

  • Serum osteoprotegerin (OPG) concentration

    Blood samples are collected at pre- (baseline), immediately post, 1-hour post drop-landing/control exercise in main trials.

  • Serum irisin concentration

    Blood samples are collected at pre- (baseline), immediately post, 1-hour post drop-landing/control exercise in main trials.

  • Circulating extracellular vesicle (EV) particle concentration and size

    Blood samples are collected at pre- (baseline), immediately post, 1-hour post drop-landing/control exercise in main trials.

  • Ground reaction force during drop-landing exercise

    Ground reaction force is recorded during each drop-landing exercise.

Study Arms (2)

Arm Drop-landing + Control

EXPERIMENTAL

According to the results of random allocation, participants first perform the drop-landing trial, followed by the control trial, with a minimum interval of one week between the two trials.

Behavioral: Exercise

Arm Control + Drop-landing

EXPERIMENTAL

According to the results of random allocation, participants first perform the control trial, followed by the drop-landing trial, with a minimum interval of one week between the two trials.

Behavioral: Exercise

Interventions

ExerciseBEHAVIORAL

During the drop-landing trial, participants perform drop-landing exercises from a block calibrated to generate approximately four times their body weight in vertical ground reaction force upon landing, employing a stiff-landing technique. Each repetition is separated by a 30-second interval, and 10 repetitions are performed as 1 set, totalling 6 sets. There is a 2-minute rest break between each set, during which the participants are asked to sit on a chair. The entire drop-landing exercise is recorded on the force plate. During the control trial, participants are required to walk up and down from the same height block without the requirement to perform the drop-landing movement. The number of repetitions, intervals, and rest breaks are completely consistent with the drop-landing exercise.

Arm Control + Drop-landingArm Drop-landing + Control

Eligibility Criteria

Age18 Years - 35 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • years old
  • Healthy
  • Male
  • Body mass index (BMI) of 18.5-29.9
  • Can understand and follow trial instructions

You may not qualify if:

  • Have any uncontrolled cardiovascular or respiratory disease
  • Have severe musculoskeletal or neurological disease likely to affect ability to perform an exercise
  • Have medical conditions known to affect musculoskeletal health
  • Have medications known to affect bone metabolism (e.g., corticosteroids, thyroxine, antiepileptic, and antiretroviral agents)
  • Regular (more than once per week) participation in high-intensity resistance or impact-type exercise in the past 6 months
  • Current smoker or vaper

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Loughborough University

Loughborough, Leicestershire, LE11 3TU, United Kingdom

Location

MeSH Terms

Conditions

Motor Activity

Interventions

Exercise

Condition Hierarchy (Ancestors)

Behavior

Intervention Hierarchy (Ancestors)

Motor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Study Officials

  • Katherine Brooke-Wavell

    Loughborough University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

November 14, 2025

First Posted

November 24, 2025

Study Start

January 15, 2024

Primary Completion

December 31, 2025

Study Completion

December 31, 2025

Last Updated

November 24, 2025

Record last verified: 2025-11

Locations