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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT02548988
Other study ID # 056711/2015
Secondary ID
Status Enrolling by invitation
Phase N/A
First received September 10, 2015
Last updated September 11, 2015
Start date October 2015
Est. completion date December 2015

Study information

Verified date September 2015
Source Universidade Federal do Rio Grande do Norte
Contact n/a
Is FDA regulated No
Health authority Brazil: Ethics Committee
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 40
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 28 Years
Eligibility Inclusion Criteria:

- 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.

Exclusion Criteria:

- Individuals experiencing pain during collection procedures

- do not perform exercises as instructed by the researches

Study Design

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Neuromuscular Electrical Stimulation
Selective Neuromuscular Electrical Stimulation on VMO

Locations

Country Name City State
Brazil Universidade Federal do Rio Grande do Norte Natal Rio Grande do Norte

Sponsors (1)

Lead Sponsor Collaborator
Universidade Federal do Rio Grande do Norte

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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 Yes
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