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Neurodynamic Mobilization and Foam Rolling

NCT03160937 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 32

Last updated 2017-05-19

No results posted yet for this study

Summary

The purpose of this study was to assess the acute effects of a single NM treatment session on DOMS and to compare them with those of one foam roller (FR) session. Following the damaging plyometric exercise bout, the participants were randomly assigned in a counter-balanced fashion to either a FR or NM treatment group; treatments were administered 48-h post-exercise. The dependent variables were recorded before the exercise, 48-h post-exercise before treatment, and immediately post-treatment.

Conditions

Interventions

OTHER

Manual therapy

The subjects repeated this motion for 1 min, rested for 30 s, and then repeated it again for 5 sets.

Sponsors & Collaborators

  • Centro Universitario La Salle

    lead OTHER

Principal Investigators

  • Daniel Muñoz, PhD · Centro Universitario La Salle

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-01-10
Primary Completion
2017-03-10
Completion
2017-04-10

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Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03160937 on ClinicalTrials.gov