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Effectiveness of the Transitional Care Model in Total Knee Arthroplasty Patients

Not Applicable
Completed
Conditions
Knee Osteoarthritis
Self Efficacy
Pain
Health Care Utilization
Interventions
Other: Transitional care model
Registration Number
NCT05525793
Lead Sponsor
Hasan Kalyoncu University
Brief Summary

The aim of this study was to determine the effectiveness of transitional care in patients with total knee arthroplasty on patients' functional status, perceived self-efficacy, and health care use. Based on the sampling inclusion criteria, we assigned the patients who would undergo knee arthroplasty to the control (n=35) and intervention (n=35) groups, via the block randomization method. The intervention group received transitional care, while the control group received usual care. Data were collected on post-intervention functional status, level of self-efficacy, and hospital visits outside of routine control.

Detailed Description

This randomised control study was conducted 70 eligible partients with total knee arthroplasty in a public hospital orthopedic and traumatology service. Participants were randomly assigned to receive either the 6-week 'Transitional Care Model' program or usual care. Assessments of self-efficacy and functional status of patients were conducted at baseline, 2nd and 9th weeks after discharge. Time-dependent changes in patient outcomes were assessed by using Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) and Arthritis Self-efficacy Scale (ASES) measurements tools. Assessments of hospital visits outside of routine control were conducted 2nd week, 6th week, 9th week, and 12th weeks after discharge. The functional status of the intervention group patients improved more than the control group according to WOMAC mean scores. Intervention group patients receiving transitional care had higher mean scores at the 2nd-week and 9th-week postoperatively in perceived self-efficacy . Besides, the rate of admission to the hospital in the intervention group was lower compared to the control group, and a significant difference was observed in the 6th-week follow-up.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
70
Inclusion Criteria
  • Having decided to undergo total knee arthroplasty for the first time due to osteoarthritis
  • Volunteering to participate in the research, not having a psychological, physical, and mental disability that may prevent communication, not having any major chronic problems such as end-stage organ failure, kidney, neurological, cancer
  • Being discharged to the home from a hospital
  • Being able to speak Turkish
  • Being available by phone
  • Being aged 50 and over
Exclusion Criteria
  • Unwillingness to continue the study
  • Rehospitalization
  • Exposure to a disease or trauma that would affect functional independence during the study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Transitional careTransitional care modelThis group is the actual intervention group.
Primary Outcome Measures
NameTimeMethod
Arthritis Self-efficacy Scale (ASES)up to 9 weeks

Assessments of self-efficacy of patients were conducted at baseline, 2nd and 9th weeks after discharge.

Western Ontario and McMaster Universities Osteoarthritis Index-WOMACup to 9 weeks

Assessments of functional status of patients were conducted at baseline, 2nd and 9th weeks after discharge.

Secondary Outcome Measures
NameTimeMethod
number of hospital visitsup to 12 weeks

Assessments of the number of hospital visits outside of routine control were conducted 2nd week, 6th week, 9th week, and 12th weeks after discharge.

Trial Locations

Locations (1)

Mustafa Kemal Üniversitesi

🇹🇷

Antakya, Hatay, Turkey

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