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Effects of Clinical Interventions for the Management of Late Start

Effects of Clinical Interventions for the Management of Late Start Muscular Pain (Doms) in the Post-exercise Recovery Process

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04628403
Enrollment
50
Registered
2020-11-13
Start date
2020-11-20
Completion date
2021-03-20
Last updated
2020-11-13

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

Conditions

Athletes

Keywords

Lasertherapy, Shockwaves, Massage, Sports Medicine, Athletic Performance

Brief summary

Introduction: Late-onset muscle pain (DOMS) is characterized by a type of temporary muscle damage, common after high-intensity exercise. In addition to pain, DOMS clinically generates muscle stiffness, reduced joint range of motion, muscle weakness and reduced peak torque. In this regard, in order to accelerate the recovery of body systems and treat symptoms of DOMS, the management of different types of interventions has been observed, supporting the clinical practice, based on evidence. Objectives: To investigate the effect of different types of clinical interventions for the treatment of DOMS. Material and methods: For the clinical trial, 50 ultramarathon and rowing athletes of both sexes, aged between 18 and 60 years old, will be recruited randomly into four possible groups: control (CG), shock waves (G1) , massage (G2) and laser therapy (G3). The evaluation moments will be as follows: minutes before exercise (M1); immediately after exercise (M2); immediately after applying the recovery technique (M3); and 24 hours after exercise (M4) and the evaluated outcomes will be: pain, psychological aspects, functional test and blood markers.

Interventions

OTHERmassage

clinical interventions, of mechanophysiological origin for the treatment of symptoms corresponding to DOMS, after exercise

lasertherapy

shock waves

Sponsors

São Paulo State University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

the results assessor will not be aware of the subject allocation group

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Professional athletes; * Age over 18 years; * Both sexes; * Not having recent injuries

Exclusion criteria

* Participants who do not complete all the proposed collection moments * who do not agree to participate will be excluded.

Design outcomes

Primary

MeasureTime frameDescription
PAIN7 dayspain systemic and located in quadriceps, assessed using a visual analog scale (0-10), with 0 indicating no pain and 10 the worst possible pain
SATISFACTION7 daysBrunel's Mood Scale (BRUMS), with ratings from 0 to 4 where, 0 represents nothing; 1 represents a little, 2 indicates moderately; 3 reports a lot; and 4 corresponds to extremely

Secondary

MeasureTime frameDescription
MUSCLE STRENGTH7 daysmeasured through a functional test entitled sit and stand. It is a test initially developed by researchers at UFRJ that consists of asking the subject to try to sit and stand in sequence, with the guidance of not using any support, for example the help of the hands or knees to obtain additional balance, leaving thus, that the musculature alone performs the function recruited

Countries

Brazil

Contacts

Primary ContactRoberto L Nahon, Dr
robertonahon@gmail.com+5521981112880
Backup ContactJaqueline S Lopes, Dra
jaqueee-santosss@hotmail.com+8069221843

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026