- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01360281
Neuromuscular Electrical Stimulation and Strength Training in Patients With Knee Osteoarthritis
May 23, 2011 updated by: Universidade Gama Filho
The purpose of this study is to compare the efficiency of neuromuscular electrical stimulation and of resisted exercises on increasing quadriceps strength, decreasing pain and on recovering motor function of patients with knee osteoarthritis.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Anticipated)
34
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Thais Dadalto, Physical Therapist
- Phone Number: 55 21 81988001
- Email: tvdadalto@hotmail.com
Study Locations
-
-
-
Rio de Janeiro, Brazil
- Recruiting
- Clinica Escola de Fisioterapia da Universidade Gama Filho
-
Contact:
- Elirez Silva, Doctor
- Email: elirezsilva@ugf.com.br
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
38 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- American College of rheumatology criterion for osteoarthritis diagnosis
Exclusion Criteria:
- Patients that have done knee replacement or are about to do.
- Patients with health conditions that are not compatible with the interventions
- Patients that have done intraarticular corticoid
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Control
|
|
Experimental: ECR
|
Resisted exercises
|
Experimental: NMES
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Change in Quadriceps strength
Time Frame: Before and after an 8 weeks intervention
|
Before and after an 8 weeks intervention
|
Change in Pain
Time Frame: Before and after an 8 weeks intervention
|
Before and after an 8 weeks intervention
|
Change in Moving function
Time Frame: Before and after an 8 weeks intervention
|
Before and after an 8 weeks intervention
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2011
Primary Completion (Anticipated)
October 1, 2011
Study Completion (Anticipated)
October 1, 2011
Study Registration Dates
First Submitted
May 19, 2011
First Submitted That Met QC Criteria
May 23, 2011
First Posted (Estimate)
May 25, 2011
Study Record Updates
Last Update Posted (Estimate)
May 25, 2011
Last Update Submitted That Met QC Criteria
May 23, 2011
Last Verified
May 1, 2011
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CAAE00780312000-10
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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