Efficacy of Proprioceptive Neuromuscular Facilitation Exercise Programme in Patients With Total Knee Arthroplasty

Last updated: March 25, 2024
Sponsor: Muğla Sıtkı Koçman University
Overall Status: Active - Recruiting

Phase

N/A

Condition

Knee Surgery

Knee Replacement

Treatment

Rehabilitation

Clinical Study ID

NCT05999864
FethiyeTDAPNF
  • Ages > 60
  • All Genders

Study Summary

This study was planned to investigate the effectiveness of usual care and proprioceptive neuromuscular facilitation exercise program in patients undergoing total knee arthroplasty surgery. It is aimed to evaluate pain intensity, disability level, proprioception, kinesiophobia, balance, range of motion and functional status of the patients. The study will be conducted with volunteer patients who are followed up by the Orthopedics and Traumatology outpatient clinic of Fethiye State Hospital and who have undergone total knee arthroplasty surgery. The evaluations will be performed in the Orthopedics and Traumatology outpatient clinic of Fethiye State Hospital. It is aimed to evaluate at least 32 patients for the study. The first evaluation will be performed 6 weeks post-operatively and the second evaluation will be performed 2 months after the treatment.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Having undergone unilateral total knee arthroplasty surgery and being 6 weekspostoperative
  • Participate in all necessary follow-up assessments
  • 60 years of age or older
  • Understand simple commands
  • Signing the consent form

Exclusion

Exclusion Criteria:

  • A previous history of total knee arthroplasty
  • Presence of revision surgery
  • Presence of severe osteoarthritis in the contralateral knee
  • Severe acute metabolic neuromuscular and cardiovascular diseases
  • Extreme obesity (bki>35)
  • Presence of malignancy
  • Have any other orthopedic or neurological problem that may affect treatment andassessments
  • Situations that prevent communication
  • Lack of cooperation during the study

Study Design

Total Participants: 32
Treatment Group(s): 1
Primary Treatment: Rehabilitation
Phase:
Study Start date:
June 08, 2023
Estimated Completion Date:
January 01, 2026

Connect with a study center

  • Fethiye State Hospital

    Muğla, Fethiye
    Turkey

    Active - Recruiting

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