NCT07354204

Brief Summary

The goal of this clinical trial is to compare recovery and impact on acute adaptation conferred by the RBE following eccentric exercise in healthy, active participants. The main questions it aimed to answer were whether 7 day supplementation with Vistula tart cherries attenuated:

  • muscle function
  • inflammation
  • soreness Participants will either consume a spray-dried tart cherry supplement or a calorie-matched placebo-control for 7 days, and complete two bouts of eccentric exercise to the elbow flexors. Participants will perform functional tests, be assessed for their perceptual recovery and markers of inflammation and muscle damage via:
  • maximal voluntary contractions
  • visual analog scales to assess soreness
  • blood samples

Trial Health

87
On Track

Trial Health Score

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

Enrollment
21

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2023

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

March 1, 2023

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2023

Completed
1.8 years until next milestone

First Submitted

Initial submission to the registry

September 27, 2025

Completed
4 months until next milestone

First Posted

Study publicly available on registry

January 21, 2026

Completed
Last Updated

January 21, 2026

Status Verified

January 1, 2026

Enrollment Period

8 months

First QC Date

September 27, 2025

Last Update Submit

January 14, 2026

Conditions

Keywords

Repeated bout effectexercise recoverytart cherrymuscle damage

Outcome Measures

Primary Outcomes (1)

  • Maximal Voluntary Contraction

    Maximal voluntary contraction measures the force capacity of the forearm flexor muscles

    Measurements were taken on 8 separate occasions. Once at baseline, 24 hour 48 hours and 72 hours after the damage protocol (Bout 1) then repeated again for Bout 2, two weeks later.

Secondary Outcomes (5)

  • Active Muscle Soreness

    Measurements were taken on 8 separate occasions. Once at baseline, 24 hour 48 hours and 72 hours after the damage protocol (Bout 1) then repeated again for Bout 2, two weeks later.

  • Pain Pressure Threshold

    Measurements were taken on 8 separate occasions. Once at baseline, 24 hour 48 hours and 72 hours after the damage protocol (Bout 1) then repeated again for Bout 2, two weeks later.

  • Limb Girth

    Measurements were taken on 8 separate occasions. Once at baseline, 24 hour 48 hours and 72 hours after the damage protocol (Bout 1) then repeated again for Bout 2, two weeks later.

  • Range of Motion

    Measurements were taken on 8 separate occasions. Once at baseline, 24 hours 48 hours and 72 hours after the damage protocol (Bout 1) then repeated again for Bout 2, two weeks later.

  • Serum Concentration of Creatine Kinase

    Measurements were taken on 8 separate occasions. Once at baseline, 24 hours 48 hours and 72 hours after the damage protocol (Bout 1) then repeated again for Bout 2, two weeks later.

Study Arms (2)

Vistula Tart Cherry

ACTIVE COMPARATOR

Supplemented with tart cherries.

Dietary Supplement: Tart Cherry

Placebo

PLACEBO COMPARATOR

Supplemented with a calorie matched placebo.

Other: Placebo

Interventions

Tart CherryDIETARY_SUPPLEMENT

7 day supplementation

Vistula Tart Cherry
PlaceboOTHER

7 day supplementation

Placebo

Eligibility Criteria

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

You may qualify if:

  • Healthy
  • Active

You may not qualify if:

  • Food allergy
  • Smokers
  • Cardiovascular/gastrointestinal/thyroid/renal disease
  • Musculoskeletal injury

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Northumbria University

Newcastle upon Tyne, Tyne and Wear, NE1 8ST, United Kingdom

Location

Study Officials

  • Glyn Howatson

    Northumbria Univeristy

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor Glyn Howatson

Study Record Dates

First Submitted

September 27, 2025

First Posted

January 21, 2026

Study Start

March 1, 2023

Primary Completion

November 1, 2023

Study Completion

December 1, 2023

Last Updated

January 21, 2026

Record last verified: 2026-01

Data Sharing

IPD Sharing
Will not share

Locations