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NCT01360281 Clinical Trial

Neuromuscular Electrical Stimulation and Strength Training in Patients With Knee Osteoarthritis

Knee Osteoarthritis Clinical Trial

Official title:
Neuromuscular Electrical Stimulation and Strength Training in Patients With Knee Osteoarthritis

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT01360281
Other study ID # CAAE00780312000-10
Secondary ID
Status Recruiting
Phase N/A
First received May 19, 2011
Last updated May 23, 2011
Start date May 2011
Est. completion date October 2011

Study information
Verified date May 2011
Source Universidade Gama Filho
Contact Thais Dadalto, Physical Therapist
Phone 55 21 81988001
Email tvdadalto@hotmail.com
Is FDA regulated No
Health authority Brazil: National Committee of Ethics in Research
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Recruiting
Enrollment 34
Est. completion date October 2011
Est. primary completion date October 2011
Accepts healthy volunteers No
Gender Both
Age group 38 Years and older
Eligibility 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 Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Other:
• Neuromuscular Electrical Stimulation

• ECR
Resisted exercises

Locations
Country Name City State
Brazil Clinica Escola de Fisioterapia da Universidade Gama Filho Rio de Janeiro

Sponsors (1)
Lead Sponsor Collaborator
Universidade Gama Filho

Country where clinical trial is conducted

Brazil, 

Outcome
Type Measure Description Time frame Safety issue
Primary Change in Quadriceps strength Before and after an 8 weeks intervention
Primary Change in Pain Before and after an 8 weeks intervention
Primary Change in Moving function Before and after an 8 weeks intervention
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