Gamification in Knee Replacement Rehabilitation

NCT03717727 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 52

Last updated 2023-07-12

No results posted yet for this study

Summary

After total knee arthroplasty (TKA), knee is usually swollen, painful, and stiff. The main goal of post-operative physical rehabilitation is to achieve full extension and flexion of the knee to avoid contractures and stiffness. Also strengthening of quadriceps muscle and balance to help activities of daily living and overall mobility are important. The post-operative knee replacement rehabilitation includes the standard protocol in hospital phase and the standard home exercise instructions. Computer based exercising games (exergames) may be new method to increase training adherence and volume after TKA and thus improve results and effectiveness of the rehabilitation. However, evidence of effectiveness of rehabilitative exergaming on physical functioning is sparse and more research is needed to conduct evidence-based rehabilitation practices.

Therefore the present study examines the effectiveness of a 16-week gamified physiotherapy on physical functioning, life satisfaction and pain for patients after TKA compared to treatment as usual home exercise. The second objective is to validate the psychometric properties of WHODAS 2.0 (WHO Disability Assessment Schedule) and brief ICF (International classification of functioning, disability and health) core set of osteoarthritis questionnaire. Other objectives are to find out, what kind of understanding and experiences the participants have about the rehabilitation with exergames and to evaluate the usability and user experience of exergames.

Conditions

Interventions

OTHER

Exergame

16-week home-based exercise intervention with exergaming system and usual treatment.

OTHER

Control

16-week home-based exercise by standard protocol and usual treatment.

Sponsors & Collaborators

  • Turku University Hospital

    collaborator OTHER_GOV
  • Turku University of Applied Sciences

    collaborator UNKNOWN
  • Jyväskylä Central Hospital

    collaborator OTHER
  • University of Oulu

    collaborator OTHER
  • University of Jyvaskyla

    lead OTHER

Principal Investigators

  • Keijo Mäkelä · Turku University Hospital

  • Ari Heinonen · University of Jyvaskyla

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
60 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-11-27
Primary Completion
2021-03-24
Completion
2022-01-17

Countries

  • Finland

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03717727 on ClinicalTrials.gov