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Efficacy of Real-time Feedback Exercise Therapy in Patients Following Total Hip Arthroplasty

NCT06161194 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 38

Last updated 2025-08-08

No results posted yet for this study

Summary

This pilot cluster-randomized, two-arm parallel-group controlled trial, aims at enhancing the understanding of the effects of real-time feedback on functional deficits as knee valgus thrust, pelvic drop, and lateral trunk lean after total hip arthroplasty. Biomechanical and patient-reported outcomes will be assessed after a total hip arthroplasty as well as at three and six months follow-ups. The primary research question is, whether digital real-time feedback supported home-exercising improves the control of the frontal knee range of motion, pelvic obliquity, and lateral trunk lean, superior to exercising supported by written instructions as comparator. The secondary aspect focuses on potential differences between groups concerning aspects of quality of life, function, and physical activity. Tertiary functional outcomes between groups will be compared for reasons of quantification movement quality.

Conditions

  • Hip Replacement

Interventions

OTHER

Supervised group exercise therapy

Participants will participate in a 90 minutes supervised group exercise therapy program 2 times a week for 8 consecutive weeks.

Sponsors & Collaborators

  • Orthopedic Hospital Vienna Speising

    collaborator OTHER

  • Klaus Widhalm

    lead OTHER

Principal Investigators

  • Klaus Widhalm · FH Campus Wien, University of Applied Sciences

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2024-01-10
Primary Completion
2025-04-15
Completion
2025-05-05

Countries

  • Austria

Study Locations

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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 NCT06161194 on ClinicalTrials.gov