Clinical Trials Directory

Trials / Completed

CompletedNCT01440972

Assessment of Efficacy of Low Intensity Resistance Training in Women at Risk for Symptomatic Knee Osteoarthritis

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
45 (actual)
Sponsor
University of Iowa · Academic / Other
Sex
Female
Age
45 Years – 65 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to asses the efficacy of a 4 week low-intensity resistance training program with concurrent application of partial blood flow restriction (PBFR) to the exercising limbs to improve quadriceps strength and size, leg muscle power, and mobility in women at risk for developing symptomatic knee osteoarthritis. The primary outcome will be change in isotonic double leg-press 1 repetition maximum (1RM) strength. The investigators will test the following hypotheses. In comparison with low-intensity resistance training without use of PBFR, a four-week low-intensity resistance-training program with PBFR will: Primary Hypothesis: Increase (a) double leg-press 1RM strength and (b) isokinetic knee extensor strength Secondary Hypotheses: 1. Increase quadriceps muscle volume assessed by MRI 2. Increase lower limb muscle power on (a) double leg-press at 40% 1RM and (b) a timed stair climb 3. Not adversely effect knee pain or quality of life assessed by the Knee injury and Osteoarthritis Outcome Score (KOOS) questionnaire

Conditions

Interventions

TypeNameDescription
OTHERpartial blood flow restriction (PBFR)low intensity resistance training with partial blood flow restriction 3 times/week for 4 weeks.
OTHERlow intensity resistance traininglow intensity resistance training without partial blood flow restriction

Timeline

Start date
2011-09-01
Primary completion
2011-11-01
Completion
2011-11-01
First posted
2011-09-27
Last updated
2016-12-05
Results posted
2015-07-30

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01440972. Inclusion in this directory is not an endorsement.