NCT03160937

Brief 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.

Trial Health

100
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
32

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Jan 2017

Shorter than P25 for not_applicable

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 10, 2017

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 10, 2017

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

April 10, 2017

Completed
1 month until next milestone

First Submitted

Initial submission to the registry

May 13, 2017

Completed
6 days until next milestone

First Posted

Study publicly available on registry

May 19, 2017

Completed
Last Updated

May 19, 2017

Status Verified

May 1, 2017

Enrollment Period

2 months

First QC Date

May 13, 2017

Last Update Submit

May 17, 2017

Conditions

Keywords

pain

Outcome Measures

Primary Outcomes (1)

  • Pain

    the numeric pain-rating scale (NPRS)

    1 minute after treatment

Secondary Outcomes (2)

  • Leg dynamometer measurements

    2 minutes after treatment

  • Surface electromyography (sEMG)

    5 minutes after treatment

Study Arms (2)

Manual therapy Foam

EXPERIMENTAL

The subjects included rolled the foam roller down their quadriceps using short kneading-like motions until it was just above their patellae, and then rolled it back to its initial position in one fluid motion. The subjects repeated this motion for 1 min, rested for 30 s, and then repeated it again for 5 sets

Other: Manual therapy

Manual therapy Nerve

ACTIVE COMPARATOR

The subjects was positioned lying on his/her side with a pillow underside leg (without fully flexing it) and the cervical and thoracic spines flexed. The investigator flex the knee and the hip extended and then put it back to its initial position in one fluid motion. The subjects repeated this motion for 1 min, rested for 30 s, and then repeated it again for 5 sets

Other: Manual therapy

Interventions

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

Manual therapy FoamManual therapy Nerve

Eligibility Criteria

Age18 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • All subjects were moderately active (Category 2) as assessed by the International Physical Activity Questionnaire (IPAQ) questionnaire (Craig et al., 2003).
  • None of the subjects had a recent history of intensive training, heavy eccentric resistance, or plyometric exercise, and all subjects were free from musculoskeletal disorders in the last year.
  • All subjects were asked to refrain from unaccustomed exercise during the experimental period, and the subjects abstained from all medications and dietary supplements during the experimental period and between testing sessions.

You may not qualify if:

  • Sedentary
  • patients with pain

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Movement DisordersNeuralgiaPain

Interventions

Musculoskeletal Manipulations

Condition Hierarchy (Ancestors)

Central Nervous System DiseasesNervous System DiseasesPeripheral Nervous System DiseasesNeuromuscular DiseasesNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Complementary TherapiesTherapeuticsPhysical Therapy ModalitiesRehabilitation

Study Officials

  • Daniel Muñoz, PhD

    Centro Universitario La Salle

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
One single evaluator who was blinded to the group assignments performed all tests that occurred 5 minutes prior to and 5 minutes after the intervention.
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: a single NM treatment session on Delayed Onset Muscle pain (DOMS) and to compare them with those of one foam roller (FR) session
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
PhD

Study Record Dates

First Submitted

May 13, 2017

First Posted

May 19, 2017

Study Start

January 10, 2017

Primary Completion

March 10, 2017

Study Completion

April 10, 2017

Last Updated

May 19, 2017

Record last verified: 2017-05

Data Sharing

IPD Sharing
Will not share