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Comparison of Early Whole Body Vibration and Progressive Resistance Training in Fast-Track Total Knee Arthroplasty.

P

Pamukkale University

Status

Completed

Conditions

Knee Arthropathy

Treatments

Procedure: Total Knee Arthroplasty
Other: Whole Body Vibration
Other: Progressive Resistance Training

Study type

Interventional

Funder types

Other

Identifiers

NCT04831411
WBV-PRE training after TKA

Details and patient eligibility

About

Patients who have undergone total knee arthroplasty (TKA) with Fast-Track recovery protocol at the Department of Orthopedics and Traumatology at the Local University Hospital and meet the inclusion and exclusion criteria will constitute the study sample. The patients will be divided into 2 groups using the computerized randomization method in the post-operative 4th week; Whole Body Vibration Group and Progressive Resistance Exercise Group. The first evaluation of the participants will be made at the end of the post-operative 4th week. Final evaluations will be made at the end of the post-operative 10th week, following the 6-week training.

Full description

Patients who have undergone total knee arthroplasty (TKA) with Fast-Track recovery protocol at the Department of Orthopedics and Traumatology at the Local University Hospital and meet the inclusion and exclusion criteria will constitute the study sample. The patients will be divided into 2 groups using the computerized randomization method in the post-operative 4th week; Whole Body Vibration Group and Progressive Resistance Exercise Group. The first evaluation of the participants will be made at the end of the post-operative 4th week. After 2 days and 6 weeks of training a week, final evaluations will be made at the end of the 10th postoperative week. Evaluations will include measures of impairment in body functions and structures, activity limitation measures, balance assessment, and quality of life assessments. Evaluations will be made by a blind researcher. The study will be started with a total of 28 patients, including 14 participants in both groups. The sample size was determined by performing a power analysis. The purpose of the study will be explained to the patients by the researcher and the patients who agree to participate in the planned study will be included in the study.

Enrollment

34 patients

Sex

All

Ages

50 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Undergoing unilateral TKA surgery due to knee OA,
  • Being between the ages of 50-75,
  • To be able to understand the verbal and written information given.

Exclusion criteria

  • To undergo revision TKA surgery.
  • Participating in any exercise or strengthening training within the last 3 months.
  • Having undergone major surgery on the extremity to be operated on.
  • Having a comorbid disease such as rheumatoid arthritis, cancer.
  • Having a neurological disease that causes functional insufficiency.
  • Having a diagnosed psychiatric disorder.
  • Having received anaesthesia for any reason in the last 1 month.
  • Regularly using hypnotics or anxiolytics.
  • Having dementia.
  • Having a hearing or vision impairment that cannot be corrected with a hearing aid or glasses.
  • Being morbidly obese (Body mass index> 40 kg/m2).
  • Having implanted pacemakers or defibrillators.
  • Having dermatological problems affecting the thigh.
  • Having a score above 3 in the American Society of Anesthesiologists classification score.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

34 participants in 2 patient groups

Whole Body Vibration
Active Comparator group
Description:
The training program will last 2 days a week and 6 weeks in total. Each session includes a warm-up, progressive whole-body vibration training and a cooling exercise. On the remaining days of the week, all patients will apply the standard exercise program, which includes simple home exercises, at home.
Treatment:
Other: Whole Body Vibration
Procedure: Total Knee Arthroplasty
Progressive Resistance Training
Active Comparator group
Description:
The training program will last 2 days a week and 6 weeks in total. Each session includes a warm-up, progressive resistance training and a cooling exercise. On the remaining days of the week, all patients will apply the standard exercise program, which includes simple home exercises, at home.
Treatment:
Other: Progressive Resistance Training
Procedure: Total Knee Arthroplasty

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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