Prehabilitation Using Aquatic Exercise

Osteoarthritis, Knee Clinical Trial

Official title:

The Effects of Aquatic Prehabilitation in Knee OA Patients on Knee Arthroplasty Outcomes

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02773745
• Other study ID #: IRB00032580
• Status: Completed
• Phase: N/A
• Start date: April 2016
• Est. completion date: January 19, 2018

Study information

• Verified date: June 2019
• Source: Wake Forest University Health Sciences
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

With aging population, total knee arthroplasty is performed with increasing frequency. Although the surgery is successful in general, significant number of patients suffers persistent pain and disability. Traditional risk assessment tool have been focused on single organ systems. Our investigators have found that mobility, assessed by the Mobility Assessment Tool short form (MAT-sf), is a simple and accurate method to predict postoperative outcome, including length of stay, postoperative complications, and nursing home placement for older patients. Prehabilitation is the process of enhancing a person's functional capacity to withstand an incoming stressor. Although multiple studies have tested prehabilitation before joint replacement surgery, results have been mixed. The investigators hypothesize that patients with limited mobility are most likely to benefit from prehabilitation. The investigators plan to use individualized aquatic exercise as a prehabilitation tool to enhance compliance; the resistance of water strengthen muscle and increasing energy expenditure; the buoyancy of water provides environment where the joints are not weight bearing. The aims of the study are: 1) To evaluate the feasibility of prehabilitation using 6-8 weeks of aquatic exercise in 40 geriatric patients who are scheduled for total knee arthroplasty for osteoarthritis; 2) To examine the effects of 6-8 weeks of aquatic exercise on mobility, pain, stiffness, physical function, cognitive function and depression; inflammatory markers and 3) To estimate the effect of prehabilitation on postoperative outcomes. The investigators plan to enroll 40 patients age >50, who are scheduled for elective primary total knee replacement. Investigators will screen patients in the Preoperative Assessment Clinic and enroll patients who have decreased mobility, measured by MAT-sf. Patients will be randomized into either a prehabilitation group or a usual care group. All the participants will undergo extensive assessment on their pain, stiffness, and physical function, depression, balance and cognitive function using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), the expanded Short Physical Performance Battery (eSPPB), and Montreal Cognitive Assessment (MoCA). Serum inflammatory markers will be assessed at the baseline. The prehabilitation group will undergo 6-8 weeks of individualized aquatic exercise in a heated pool (60 min/session, 3 times per week). Aquatic equipment maybe used to challenge balance and trunk stabilization. All participants will be reassessed immediately before surgery and 4 weeks after the surgery using WOMAC, eSPPB, MoCA and MAT-sf. Serum inflammatory markers and body composition will be reassessed at the same time points. The primary outcome of interest is will be postoperative complications, length of stay, Intensive Care Unit length of stay, and institutionalization. If successful, investigators will have sound pilot data for several critical health outcomes with which to support an external proposal for a larger-scale study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44
• Est. completion date: January 19, 2018
• Est. primary completion date: January 19, 2018
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 50 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Osteoarthritis
• Osteoarthritis, Knee

Intervention

Behavioral:
• Aquatic Prehab
Pool therapy

Locations

Country	Name	City	State
United States	Clinical Research Unit	Winston-Salem	North Carolina

Sponsors (1)

Lead Sponsor	Collaborator
Wake Forest University Health Sciences

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in physical function using the MAT-sf	Change in MAT-sf score from baseline (prior to surgery) to follow up (4-6 weeks after surgery)	4-6 weeks after surgery
Primary	Change in physical function using the eSPPB	Change in eSPPB score from baseline (prior to surgery) to follow up (4-6 weeks after surgery)	4-6 weeks after surgery
Primary	Change in physical function using the Postural Sway Force Plate	Change in postural sway score from baseline (prior to surgery) to follow up (4-6 weeks after surgery)	4-6 weeks after surgery