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Pre-operative One-on-One Physical Therapy Education Improves Postoperative Function and Patient Satisfaction After Total Joint Arthroplasty

Not Applicable
Completed
Conditions
Arthroplasty
Interventions
Behavioral: Preoperative Physical Therapy Session
Behavioral: Group Preoperative Education Session (per the standard of care)
Registration Number
NCT02872337
Lead Sponsor
Hospital for Special Surgery, New York
Brief Summary

The purpose of this study was to evaluate the efficacy of a one-time, preoperative physical therapy protocol on postoperative (1) discharge disposition, (2) pain, function and stiffness and (3) patient satisfaction.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
126
Inclusion Criteria
  • Subjects will be required to meet the following inclusion criteria in order to participate:

    • Unilateral Primary Knee OA or Hip OA
    • Patients at least 18 years old up to 85.
    • Undergoing surgery with one of the following study surgeons
    • Able to independently ambulate ≥ half a block with or without assistive device
    • Able to independently perform non-reciprocal stairs with or without assistive device/rails
    • Patients that plan to D/C home post TKA / THA
    • Patients that speak English only.
Exclusion Criteria
  • Rheumatoid arthritis
  • Psoriatic arthritis
  • Juvenile rheumatoid arthritis
  • Knee or Hip revisions
  • Patients under 18 years of age
  • Patients unwilling or unable to complete PRO instrument or study questionnaires at the specified study time points pre-operatively or post-operatively
  • Bilateral TKA and THA
  • Uni-condylar knee arthroplasty or Hip resurfacing
  • Patellar reconstruction
  • Patient on disability, workman's compensation
  • Patients unwilling to participate in PEdPTWP and/or Patient education class and booklet.
  • Patients that plan to D/C to rehabilitation center post TKA and THA
  • Patients that do not speak English
  • Patients that do not have access to computer

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Experimental (Intervention): PreopPT GroupGroup Preoperative Education Session (per the standard of care)This group will undergo the group preoperative education session. Following this session (intervention) this group underwent a one-time, one-on-one preoperative PT session. They also were given access to a web-based microsite which was customized to surgeon
Control (standard of care): No PreopPT GroupGroup Preoperative Education Session (per the standard of care)This group underwent the current of standard of care at our institution. This only includes the group preoperative education session. No further preoperative education was given.
Experimental (Intervention): PreopPT GroupPreoperative Physical Therapy SessionThis group will undergo the group preoperative education session. Following this session (intervention) this group underwent a one-time, one-on-one preoperative PT session. They also were given access to a web-based microsite which was customized to surgeon
Primary Outcome Measures
NameTimeMethod
Number of In-patient Physical Therapy visits required to meet hospital discharge criteria PTThrough Study Completion, an average of 3 days

This included a review of the hospital database for hospital discharge time. At this institution PT discharge is defined as the ability to (1) independently transfer, (2) independently ambulate approximately 150 feet and (3) independently negotiate stairs (4) independent with home exercise program and activities of daily living.

All of this data was recorded from hospital records

Secondary Outcome Measures
NameTimeMethod
Hospital Length of StayTime from Surgery until Hospital Discharge, an average of 2-3 days

collected from a hospital database

Time to meet Physical Therapy discharge criteriaTime from Surgery to meeting PT discharge criteria, an average of 3 days

At this institution PT discharge is defined as the ability to (1) independently transfer, (2) independently ambulate approximately 150 feet and (3) independently negotiate stairs (4) independent with home exercise program and activities of daily living.

Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC)This standard patient reported outcome was filled out preoperatively or at six weeks postoperatively

This standard patient reported outcome was filled out preoperatively or at six weeks postoperatively

Patient Satisfaction Scoresfrom two weeks prior to surgery until 6 weeks after surgery

Patient satisfaction was measured by a series of patient administered questionnaires at various stages of the study. All satisfaction questions, with the exception of the utilization of the microsites \[Yes/No\], were asked via a visual analogue scale to disagree or agree with given statements \[0-5, where 0 was strongly disagree, 3 was neutral and 5 was strongly agree\]. Patients unable to complete any forms at the time of the appointment completed the form over the phone with a co-investigator.

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