NCT02548988

Brief Summary

The purpose of this study is analyze the immediate effect of selective neuromuscular electrical stimulation of vastus medialis obliquus (VMO) in the electrical activity of VMO and vastus lateralis (VL) and in the isokinetic performance of women with patellofemoral pain syndrome.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
40

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2015

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
unknown

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

First Submitted

Initial submission to the registry

September 10, 2015

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 14, 2015

Completed
17 days until next milestone

Study Start

First participant enrolled

October 1, 2015

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2015

Completed
Last Updated

September 14, 2015

Status Verified

September 1, 2015

Enrollment Period

2 months

First QC Date

September 10, 2015

Last Update Submit

September 11, 2015

Conditions

Outcome Measures

Primary Outcomes (1)

  • Electromyographic activity (root mean square - RMS) of vastus medialis obliquus

    The immediate effect of neuromuscular electrical stimulation will be measured through surface electromyography and the variable analyzed will be root mean square (RMS).

    Change from baseline in Electromyographic activity at 30 minutes

Study Arms (2)

Healthy

EXPERIMENTAL

Healthy women are submitted to selective neuromuscular electrical stimulation on VMO.

Other: Neuromuscular Electrical Stimulation

Patellofemoral pain syndrome

EXPERIMENTAL

Women with patellofemoral pain syndrome are submitted to selective neuromuscular electrical stimulation on VMO.

Other: Neuromuscular Electrical Stimulation

Interventions

Selective Neuromuscular Electrical Stimulation on VMO

HealthyPatellofemoral pain syndrome

Eligibility Criteria

Age18 Years - 28 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • For Healthy group:
  • with no history of osteomyoarticular lesion or surgery in the lower limbs in the previous six months
  • non-corrected neurological, vestibular, visual and/or hearing impairment
  • For Patellofemoral pain syndrome group:
  • clinical diagnosis of patellofemoral pain syndrome
  • absence of other disorders in the knee
  • refer pain at leafs two of the following activities: when remain seated for a long period, squat, kneel and go up or down stairs.

You may not qualify if:

  • Individuals experiencing pain during collection procedures
  • do not perform exercises as instructed by the researches

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Universidade Federal do Rio Grande do Norte

Natal, Rio Grande do Norte, 59078-970, Brazil

Location

MeSH Terms

Conditions

Patellofemoral Pain Syndrome

Condition Hierarchy (Ancestors)

Joint DiseasesMusculoskeletal Diseases

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NON RANDOMIZED
Masking
NONE
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor of Physiotherapy

Study Record Dates

First Submitted

September 10, 2015

First Posted

September 14, 2015

Study Start

October 1, 2015

Primary Completion

December 1, 2015

Study Completion

December 1, 2015

Last Updated

September 14, 2015

Record last verified: 2015-09

Locations