The Effects of Liquid IV's Multi-Ingredient Recovery Supplement on Muscle Recovery Following Exercise

N/ANot Yet RecruitingNCT07224867

Applied Science & Performance Institute30 enrolled

Overview

The purpose of this study is to evaluate the efficacy of a multi-ingredient recovery supplement . The research will focus on strength recovery and performance maintenance assessing reductions in soreness and inflammation, as well as muscle repair and damage mitigation. By investigating these key recovery metrics, this study aims to investigate the efficacy of this supplement as a solution for active individuals seeking to optimize post-exercise recovery.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

DOUBLE

Enrollment

Conditions

Muscle Damage Strength Recovery Perceived Recovery Perceived Muscle Soreness Physical Performance

Eligibility

Sex: ALLMin age: 18 YearsMax age: 55 YearsHealthy volunteers:

Medical Language ↔ Plain English

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.

Outcomes

Primary Outcomes

Lower Body Power and Force Generation (Maximal Countermovement Jump (CMJ))

The force plate platform consists of two force plates (left \& right) containing four force sensors which measure ground reaction force. The sensors are connected to a laptop and analyzed using Mechanography GRFP Research Edition® software (version 4.2-b05.53-RES). Subjects will perform three maximal vertical CMJs on a calibrated force plate. Subjects will be instructed to stand upright on the center of the force plate with feet shoulder-width apart and hands placed on the hips. Subjects will perform a maximal effort vertical jump with proper form and instructed to land with soft knees and remain still after each jump for data capture. A 30sec rest period will be provided between each trial. Data will be used to assess maximum force output (Fmax), rate of force development (RFD), jump height (inches), and maximum power (Pmax). Force curves will be reviewed for each trial, and results averaged. This will quantify full-body mechanical power under standardized, reproducible conditions.

Time frame: Taken at baseline testing, 24 hour, 48 hour, and 72 hour.

Lower-Body Strength (Biodex Dynamometry)

Participants will complete isometric and isokinetic strength assessments, unilaterally on the dominant leg, of knee extension (ext) and flexion (flx) using a Biodex System 4 Pro dynamometer (Biodex Medical Systems, Shirley, NY). Proper positioning and stabilization will be ensured per manufacturer guidelines. Isometric testing - knee joint will be fixed @60° of flexion. Participants will perform 3 maximal effort ext/flx contractions, each lasting 5sec, with 5sec of rest between efforts. Highest recorded torque value across the 3 trials will be analyzed. Subjects will then complete isokinetic testing consisting of 5 maximal concentric knee ext and flx at an angular velocity of 60°/s. Full range of motion will be established prior to testing. Peak torque and average torque across all 5 repetitions will be recorded for analysis. All torque values will be gravity-corrected by the system software, and same technician will conduct all tests for consistency.

Time frame: Tested at baseline, 24 hour, 48 hour, and 72 hour.

Perceived Recovery Status (PRS) Likert Scale

The PRS is a composite scale directly proportional to recovery (Laurent, et al. 2011). Hence, the purpose of the scale will be to assess the participant's recovery from the previous exercise session. Subjects will be informed that having no soreness and a high feeling of recovery is a 10, while extreme soreness and low feelings of recovery, leading to limited ability to function, is defined by a range of 0-3, adequate recovery, with some ability to function, is defined by a range of 4-7, and good recovery, with the ability to function normally, is defined by a range of 8-10.

Time frame: Taken at baseline testing, 24 hours, 48 hours, and 72 hours timepoints.

Perceived Body Soreness Likert Scale

A 7-point likert scale will be used for lower body muscle soreness, after performing 5 air squats. The Likert scale is a validated instrument designed to assess self reported muscle soreness, measured across a 7-point scale. The scale ranges from 0 (no soreness), to 6 (unbearable soreness), and has good validity and reliability (Impellizzeri, F., et al., 2007).

Time frame: Taken at baseline testing, 24 hour, 48 hour, and 72 hour timepoints.

Numeric Pain Rating Scale (NPRS)

The NPRS is a subjective 11-point numeric pain rating scale, with 0 representing "no pain" and 10 representing "unbearable pain." The Likert scale is a validated instrument designed to assess self reported pain. For this study, the subjects will be asked to assign a number to their average lower extremity joint pain (hip and knee joint pain) (Hawker et al., 2011) at the designated time points.

Time frame: NPRS will be taken at baseline, 24 hour, 48 hour and 72 hour time points

Secondary Outcomes

Body Hydration Status (InBody)

Body hydration status will be assessed using multi-frequency bioelectrical impedance analysis (BIA) (InBody 770, InBody Co., Ltd., Seoul, South Korea). The InBody device uses direct segmental multi-frequency impedance (5 kHz to 1 MHz) to estimate water distribution across body compartments. Measurements will include total body water (TBW), extracellular water (ECW), and intracellular water (ICW) to evaluate fluid compartment status. BIA assessments will be conducted under standardized conditions with participants barefoot, standing upright with arms slightly abducted, and heels positioned on the footplate electrodes. Light, non-conductive clothing will be required, and all metal (e.g., jewelry, watches) are removed before testing. To minimize fluid variability, participants will avoid food, drink, and caffeine for at least 8 hours prior to testing. Measurements will be collected pre-supplementation and post-exercise/post supplement as part of the hydration analysis at baseline only.

Time frame: taken during baseline testing only - before exercise and again at ~10 minutes post treatment