Can a drink speed up muscle recovery? new study puts liquid IV to the test
NCT ID NCT07224867
First seen Jun 25, 2026 · Last updated Jul 09, 2026 · Updated 3 times
Summary
This study will test whether a multi-ingredient recovery supplement from Liquid IV helps muscles recover faster after exercise. Thirty healthy, active adults will take either the supplement or a placebo after workouts, and researchers will measure strength, power, soreness, and hydration. The goal is to see if the supplement reduces muscle damage and speeds up recovery for people who exercise regularly.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- proprietary post-workout recovery supplement (dietary supplement)
- What this could lead to
- If it works, this could provide a convenient supplement to help active people recover faster from exercise with less soreness.
- What could go wrong
- This is a small, early-stage study with only 30 participants, and the supplement may not show significant benefits over a placebo. Results may not apply to everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 55 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Healthy males or females aged 18-55 years old. * Must be recreationally trained or trained/developmental as previously defined (McKay et al., 2021). * Able to read and write in English. * Cessation of current use of tart cherry extract, protein powders, essential amino acids/BCAAs, calcium fructoborate, boron, or anabolic agents for a minimum of 1 week prior to, and throughout the duration of the study. * Willing to maintain regular supplement routine otherwise during the trial, and will not introduce or discontinue a supplement, other than what was previously mentioned. * Will not participate in any strenuous exercise for a minimum of 1-week prior to exercise performance assessments, as well as during the days of exercise testing. Strenuous exercise as defined for this study includes ½ and full marathons (or more), heavy (i.e.,\>80% 1RM) lifting, and any high intensity, physical activity that could make your muscles sore. * During the study, you agree not to take any NSAIDs or other anti-inflammatory medications. Exclusion Criteria: * Sedentary * Highly trained/national level or professional athlete * Known diagnosis of any cardiovascular, metabolic, musculoskeletal, endocrine, or renal disease/disorder. * Recent musculoskeletal injury (\<3-months) * Recent orthopedic surgery (\<12-months) * History or current malignancy. * Current respiratory infection (i.e., cold) or high temperature (fever) within the past 4-weeks. * Previous gastrointestinal surgery within the past 12 months. * Regular smoker. * Regular drinker (\>14 drinks per week). * Those regularly using anti-inflammatory drugs within the last 4-weeks. * Current use of prescription medications that may influence adaptation to exercise (hormone therapies, peptides, etc.). * Allergies to study-related materials. * Any condition that impairs their ability to complete the required exercises. * Female subjects must not be pregnant or lactating. * Are unable to provide informed consent or are non-English speakers. * Presently using GLP-1 medications.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Applied Science & Performance Institute
Tampa, Florida, 33634, United States
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