Panacea Index Logo

Command Palette

Search for a command to run...

A randomised controlled trial assessing the potential of palmitoylethanolamide (PEA) to act as an adjuvant to resistance training in healthy adults: a study protocol.

Trials
March 31, 2023
Zoya Huschtscha et al. (16 authors)
Clinical Trial ProtocolJournal ArticleHuman StudyClinical
Study Details

Study Goal

The researchers aimed to investigate whether daily PEA supplementation (Levagen + ®) combined with resistance training affects lean body mass, strength, power, physical performance, and recovery outcomes (e.g., sleep) compared to placebo.

Results Summary

The abstract does not provide results, as the study appears to be a proposed or ongoing trial.

Population

Healthy active adults aged 18-35 years who are not resistance-trained.

Effective Dosage

Not specified in the abstract.

Duration

11 weeks (including 8 weeks of progressive resistance training).

Interactions

None mentioned

Extracted Claims (8)
InterventionDirectionEndpointPopulationDosageImpactClaim #
Non-steroidal anti-inflammatory drugs (NSAIDs) and analgesics
decrease
signalling pathways (e.g., cyclooxygenase-2)
-
-
have been shown to inhibit
#1
Non-steroidal anti-inflammatory drugs (NSAIDs) and analgesics
decrease
muscular adaptations such as hypertrophy and strength
-
-
may hinder
#2
palmitoylethanolamide (PEA)
neutral
analgesic properties
-
-
have
#3
palmitoylethanolamide (PEA)
increase
sleep
-
-
has been shown to have a positive effect on
#4
palmitoylethanolamide (PEA)
increase
muscle hypertrophy via PKB activation
-
-
may contribute positively to
#5
daily PEA supplementation (Levagen + ®) with resistance training
neutral
lean body mass, strength, power and physical performance and outcomes of recovery (e.g., sleep)
18-35 years old, healthy active adults that are not resistance trained
-
investigate the effects of
#6
Non-steroidal anti-inflammatory drugs (NSAIDs) and analgesics
decrease
muscle protein synthesis and training adaptations
-
-
may inhibit
#7
PEA
neutral
training adaptations
athletes and active individuals
-
determine if this analgesic compound interferes with or enhances
#8
Abstract

BACKGROUND: Non-steroidal anti-inflammatory drugs (NSAIDs) and analgesics are used frequently by athletes either prophylactically for the prevention of pain, or to accelerate recovery following an injury. However, these types of pain management strategies have been shown to inhibit signalling pathways (e.g., cyclooxygenase-2) that may hinder muscular adaptations such as hypertrophy and strength. Nutraceuticals such as palmitoylethanolamide (PEA) have analgesic properties that act via different mechanisms to NSAIDS/analgesics. Furthermore, PEA has been shown to have a positive effect on sleep and may contribute positively to muscle hypertrophy via PKB activation. Although PEA has not been widely studied in the athletic or recreationally active population, it may provide an alternative solution for pain management if it is found not to interfere with, or enhance training adaptations. Therefore, the study aim is to investigate the effects of daily PEA supplementation (Levagen + ®) with resistance training on lean body mass, strength, power and physical performance and outcomes of recovery (e.g., sleep) compared to placebo. METHODS: This double-blind, randomised controlled study will take place over an 11-week period (including 8-weeks of progressive resistance training). Participants for this study will be 18-35 years old, healthy active adults that are not resistance trained. Participants will attend a familiarisation (week 0), pre-testing (week 1) and final-testing (week 11). At the pre-testing and final-testing weeks, total lean body mass (dual-energy X-ray absorptiometry; DXA), total mid-thigh cross sectional area (pQCT), maximal muscular strength (1 repetition maximum bench press, isometric mid-thigh pull) and power (countermovement jump and bench throw) will be assessed. Additionally, circulating inflammatory cytokines and anabolic hormones, sleep quality and quantity (ActiGraph), pain and subjective wellbeing (questionnaires) will also be examined. DISCUSSION: This study is designed to investigate the effects that PEA may have on pre-to post intervention changes in total body and regional lean muscle mass, strength, power, sleep, subjective wellbeing, and pain associated with resistance training and menstruation compared with the placebo condition. Unlike other NSAIDs and analgesics, which may inhibit muscle protein synthesis and training adaptations, PEA which provides analgesia via alternative mechanisms may provide an alternative pain management solution. It is therefore important to determine if this analgesic compound interferes with or enhances training adaptations so that athletes and active individuals can make an informed decision on their pain management strategies. TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry (ANZCTR: ACTRN12621001726842p).

Medical Subject Headings (MeSH)
FemaleHumansAdultAdolescentYoung AdultResistance TrainingPisum sativumAustraliaMuscle StrengthAnalgesicsPainDietary SupplementsAnti-Inflammatory Agents, Non-SteroidalMuscle, SkeletalRandomized Controlled Trials as Topic
Study Links
Quality Scores
SafetyNot Assessed
Quality85/10
Citation Metrics
Total Citations2
Citations/Year1.0
Relative Citation Ratio0.69
NIH Percentile37.1%
Research Impact Scores
APT Score0.25
Weight Score2.62
Normalized Score0.57
Related Supplements
A randomised controlled trial assessing the potential of pal... | Panacea Index