Aquatic Power Training
Optimizing Mobility in Older Adults With Knee Osteoarthritis: Aquatic Power Training
1 other identifier
interventional
81
1 country
1
Brief Summary
Knee Osteoarthritis (OA) accounts for a significant proportion of mobility limitations and is one of the most disabling problems facing the growing population of older adults. The purpose of this research is to reduce disablement of older adults with symptomatic knee osteoarthritis.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable knee-osteoarthritis
Started Apr 2009
Shorter than P25 for not_applicable knee-osteoarthritis
1 active site
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
Study Start
First participant enrolled
April 1, 2009
CompletedFirst Submitted
Initial submission to the registry
May 15, 2009
CompletedFirst Posted
Study publicly available on registry
May 19, 2009
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2009
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2009
CompletedJune 25, 2010
June 1, 2010
8 months
May 15, 2009
June 24, 2010
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
400 meter walk time
0, 6, and 12 weeks
Secondary Outcomes (4)
Lower limb function (LLFDI)
0, 6, and 12 weeks
Quality of life (KOOS)
0, 6, and 12 weeks
Knee osteoarthritis pain (KOOS pain scores)
0 and 6 weeks
Vastus lateralis muscle bulk
0, 2, 6, and 12 weeks
Study Arms (1)
Aquatic
EXPERIMENTALAquatic Power Training
Interventions
Aquatic power training program with an exercise specialist 2/week for 6 weeks.
Eligibility Criteria
You may qualify if:
- Age 50 or older
- Symptomatic knee osteoarthritis (knee osteoarthritis diagnosed by the American College of Rheumatology criteria and frequent knee symptoms)
You may not qualify if:
- bilateral knee replacement
- acute or terminal illness
- unstable cardiovascular condition or other medical conditions that may impair ability to participate such as pulmonary disease requiring use of supplement oxygen, or lower limb musculoskeletal surgery in the past 6 months
- unwilling to be in a pool (approximately 4 feet deep)
- m walk time equal to or slower than the median for sex and decade:
- M 50's 250.2 60's 289.9 70's+ 290.8
- F 50's 315.9 60's 305.2 70's+ 292.5
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The University of Iowa
Iowa City, Iowa, 52242, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Neil A Segal, MD, MS
University of Iowa
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
May 15, 2009
First Posted
May 19, 2009
Study Start
April 1, 2009
Primary Completion
December 1, 2009
Study Completion
December 1, 2009
Last Updated
June 25, 2010
Record last verified: 2010-06