Tart Cherries - The Influence on Acute Adaptation
1 other identifier
interventional
21
1 country
1
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
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Mar 2023
Shorter than P25 for not_applicable
1 active site
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 Start
First participant enrolled
March 1, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 2023
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2023
CompletedFirst Submitted
Initial submission to the registry
September 27, 2025
CompletedFirst Posted
Study publicly available on registry
January 21, 2026
CompletedJanuary 21, 2026
January 1, 2026
8 months
September 27, 2025
January 14, 2026
Conditions
Keywords
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 COMPARATORSupplemented with tart cherries.
Placebo
PLACEBO COMPARATORSupplemented with a calorie matched placebo.
Interventions
Eligibility Criteria
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
- Northumbria Universitylead
- Iprona Lana SpAcollaborator
Study Sites (1)
Northumbria University
Newcastle upon Tyne, Tyne and Wear, NE1 8ST, United Kingdom
Study Officials
- PRINCIPAL INVESTIGATOR
Glyn Howatson
Northumbria Univeristy
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