NCT07472244

Brief Summary

Eccentric exercise, particularly when novel and strenuous, can cause soreness and inflammation, impairing subsequent exercise performance. These performance decrements are attributable to oxidative stress and inflammation. Interestingly, a single bout of eccentric exercise can confer protective effects, ameliorating the negative consequences in subsequent bouts. This is termed the repeated bout effect (RBE), which would be of interest to athletes considering the detrimental effects of strenuous eccentric exercise. Athletes regularly consume supplements in hope of attenuating the performance decrements after strenuous eccentric exercise . However, considering the dose-response relationship between the initial performance decrement and the magnitude of the RBE , supplements may diminish the obtainment of the RBE. This notion remains untested, and so the proposed project is a double-blind, placebo-controlled, parallel group study aiming to assess the effects of acute vitamin C and ibuprofen supplementation on the development of the RBE. These two supplements were chosen as they are most frequently and successfully used in the literature to target oxidative stress (vitamin C) and inflammation (ibuprofen). Additionally, these doses (and the timing of supplements) were chosen to mimic protocols reporting beneficial effects

Trial Health

77
On Track

Trial Health Score

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

Enrollment
52

participants targeted

Target at P25-P50 for not_applicable

Timeline
8mo left

Started Sep 2025

Geographic Reach
1 country

1 active site

Status
recruiting

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress53%
Sep 2025Feb 2027

Study Start

First participant enrolled

September 1, 2025

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

March 4, 2026

Completed
12 days until next milestone

First Posted

Study publicly available on registry

March 16, 2026

Completed
12 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 28, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 28, 2027

Last Updated

March 16, 2026

Status Verified

February 1, 2026

Enrollment Period

1.5 years

First QC Date

March 4, 2026

Last Update Submit

March 13, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Muscle Function

    Jump height calculated through flight time

    Baseline and post exercise (2 hours, 1 day, 7 day)

Secondary Outcomes (4)

  • Muscle Function

    Baseline and post exercise (2 hours, 1 day, 7 day)

  • Muscle Function

    Baseline and post exercise (2 hours, 1 day, 7 day)

  • Muscle Function

    Baseline and post exercise (2 hours, 1 day, 7 day)

  • Creatine Kinase

    Baseline and immediately, 1-h (hour)-, 2-h-, 24-h-,and 48-hours-post-exercise

Study Arms (2)

Intervention

EXPERIMENTAL

Vitamin C and Non-steroidal anti-inflammatory drug

Dietary Supplement: Intervention

Control

PLACEBO COMPARATOR

Identical Placebo

Dietary Supplement: Control

Interventions

ControlDIETARY_SUPPLEMENT

Identical maltodextrin tablet. Appearance and weight matched

Control
InterventionDIETARY_SUPPLEMENT

1,000 mg Vitamin C and 400 mg non-steroidal anti-inflammatory drug every 8-h for 48-h

Intervention

Eligibility Criteria

Age18 Years - 45 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • years of age
  • BMI 18.5 - 29.9 kg/m2
  • Able to perform 20-minutes of bench stepping exercise
  • Capable and willing to provide consent (oral and written)

You may not qualify if:

  • Familiarised with bench stepping exercise procedures
  • Not cleared for exercise by health questionnaires or physical activity readiness questionnaire
  • Participants exhibiting any alteration in clinical inflammation parameters due to other cause
  • Participants currently being prescribed any anti-inflammatory medications

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

University of Bath

Bath, United Kingdom

RECRUITING

MeSH Terms

Interventions

Methods

Intervention Hierarchy (Ancestors)

Investigative Techniques

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Model Details: The proposed study is a randomised, double blind, placebo controlled, parallel-group study
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Chief Investigator

Study Record Dates

First Submitted

March 4, 2026

First Posted

March 16, 2026

Study Start

September 1, 2025

Primary Completion (Estimated)

February 28, 2027

Study Completion (Estimated)

February 28, 2027

Last Updated

March 16, 2026

Record last verified: 2026-02

Data Sharing

IPD Sharing
Will share

Locations