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Effects of ReWin(d) Supplementation on the Recovery of DOMS Induced by Acute Exercice

Effects of Dietary Supplementation With ReWin(d) on the Recovery of Young Athletes Suffering From Delayed-Onset Muscle Soreness Induced by Acute Exercice: A Pilot Randomized, Double-blind, Placebo Controlled Trial

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03961022
Enrollment
40
Registered
2019-05-23
Start date
2018-10-22
Completion date
2018-12-21
Last updated
2019-05-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Delayed-onset Muscle Soreness, Muscle Soreness

Keywords

DOMS, Fatigue rate, Heart rate variability, Pain, Jump performance

Brief summary

The study will assess the recovery and performance of young athletes suffering from muscle damage induced by physical exercise. Model by comparing the safety and efficacy of ReWin(d) supplemention during 4 weeks to placebo over 72 hours post exercice.

Detailed description

Double-blind, randomized, placebo controlled, parallel group, pilot safety and efficacy study. 40 healthy young male athetes were randomly assigned to the ReWin(d) or Placebo group. After 4 weeks supplementation (either 2 g daily of ReWin(d) capsules or placebo capsules). the participants were subjected to a 1 hour plyometric exercise session to induce DOMS. At 0 hours, 24 hours, 48 hours and 72 hours post exercise, the volunteers have been assessed to determine: (i) pain perception, (ii) fatigue rate, (iii) sport performance (effectiveness of a jump) and (iv) muscle damage and inflammation by I-R thermography and biomarkers

Interventions

DIETARY_SUPPLEMENTPolyherbal supplement: ReWin(d) vs Placebo

Supplementation during 4 weeks + 72 hours post acute exercice

Sponsors

European University of Madrid
CollaboratorOTHER
Natural Origins
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Intervention model description

Single dose, Randomized, Double Blinded, Placebo-controlled Study

Eligibility

Sex/Gender
MALE
Age
20 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* \> 18 years old * Young athletes * Training at least 3 times per week * Agree not to initiate any new exercise or diet programs during the entire study period * Agree not to change their current diet or exercise program during the entire study period * Agree not to stretch, utilize ice massage, take anti-inflammatory medications (eg, aspirin, ibuprofen), or use any other treatment for the duration of the trial.

Exclusion criteria

* Previous history of upper extremity injury or knee joint pain * Use of anti-inflammatory medications or pain medications 1 week before the screening visit and during the study * Daily use of dietary supplements and herbal supplements beginning at the screening visit and during the study * Antibiotic use in past 3 months * Chronic disease

Design outcomes

Primary

MeasureTime frameDescription
Effects of ReWin(d) on muscle recovery induced by physical exerciseChange from baseline at 0 hours, 24 hours, 48 hours and 72 hours post plyometric exercises session to induce DOMSSport performance (effectiveness of a jump) after exercise-induced muscle damage

Secondary

MeasureTime frameDescription
Effects of ReWin(d) on muscle damage induced by physical exerciseChange from baseline at 0 hours, 24 hours, 48 hours and 72 hours post plyometric exercises session to induce DOMSMuscle skin temperature monitored by IR-camera.
Effects of ReWin(d) on pain perception induced by physical exerciseChange from baseline at 0 hours, 24 hours, 48 hours and 72 hours post plyometric exercises sessionVisual Analogue Scale pain perception after exercise-induced muscle damage
Effects of ReWin(d) on fatigue rate induced by physical exerciseChange from baseline at 0 hours, 24 hours, 48 hours and 72 hours post plyometric exercises sessionHeart Rate Variability assessment after exercise-induced muscle damage
Effects of ReWin(d) on Gut MicrobiotaChange from baseline dose after 4 weeks of interventionDetermination of Microbiota composition by 16S rRNA Sequencing.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026