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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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12 December 2020 |
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Main ID: |
NCT02773745 |
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Date of registration:
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09/05/2016 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Prehabilitation Using Aquatic Exercise
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Scientific title:
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The Effects of Aquatic Prehabilitation in Knee OA Patients on Knee Arthroplasty Outcomes |
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Date of first enrolment:
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April 2016 |
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Target sample size:
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44 |
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Recruitment status: |
Completed |
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URL:
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https://clinicaltrials.gov/show/NCT02773745 |
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Study type:
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Interventional |
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Study design:
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Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Supportive Care. Masking: Single (Investigator).
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Phase:
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N/A
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Countries of recruitment
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United States
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Contacts
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Name:
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Sunghye Kim, MD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Wake Forest Baptist Medical Center |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- Signed Informed Consent
- Age > 50
- Willingness to exercise in a pool 3 times a week
- MAT-Sf score = 58 for men and = 50 for women
- Participant is scheduled for primary total knee replacement surgery due to OA >4 weeks
from expected BV visit
- Not involved in any other behavioral, exercise or investigational drug intervention
study
Exclusion Criteria:
- Impaired cognitive function (MoCA <21)
- Undergoing knee replacement surgery for indications other than OA
- Undergoing bilateral knee replacements
- Major deficits in hearing or vision
- Currently exercising more than 3 times per week
- Severe depression (GDS-sf = 12)
- Contraindications to the pool: open wounds/ incontinence/history of seizures in last
year
Age minimum:
50 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Osteoarthritis, Knee
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Intervention(s)
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Behavioral: Aquatic Prehab
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Primary Outcome(s)
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Change in physical function using the eSPPB
[Time Frame: 4-6 weeks after surgery]
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Change in physical function using the MAT-sf
[Time Frame: 4-6 weeks after surgery]
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Change in physical function using the Postural Sway Force Plate
[Time Frame: 4-6 weeks after surgery]
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Secondary ID(s)
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IRB00032580
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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