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NCT07260318

Acute Effects of Cricket Fast Bowling on Bone Turnover and Signaling Markers

ENROLLING BY INVITATION NA Last updated 3 December 2025
What this trial tests

NA trial testing Exercise in Health Adults in 14 participants. Enrolling by invitation.

Timeline
20 February 2023
Primary endpoint
31 December 2025
31 December 2025

Quick facts

Lead sponsorLoughborough University
PhaseNA
StatusENROLLING BY INVITATION
Study typeINTERVENTIONAL
Allocationnon randomized
Designcrossover
Maskingnone
Primary purposebasic science
Enrollment14
Start date20 February 2023
Primary completion31 December 2025
Estimated completion31 December 2025
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Loughborough University

Who can join

Adults 18 to 30, male only, with Health Adults. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this study is to investigate the acute effects of cricket fast bowling on the bone turnover and signaling markers in healthy young males. The main question aims to answer: • Does a single bout acute fast bowling change serum C-terminal telopeptide of type I collagen (CTX-I) and other bone turnover and signaling markers levels? Participants complete both the bowling and control trials, 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 2-hour post bowling/rest.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Exercise

Trials testing the same drug.

Other recruiting trials for Health Adults

Currently open trials in the same condition.

Other Loughborough University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07260318.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing