ReMove-It - Efficacy study of rehabilitation with telemedical assisted movement therapy after lower extremity interventio

Not Applicable

• Conditions: Patients after total knee or hip arthroplasty; Other primary gonarthrosis; M16.1; M17.3; Other primary coxarthrosis; M17.1; M16.5; Other post-traumatic coxarthrosis; Other post-traumatic gonarthrosis

• Registration Number: DRKS00010009
• Lead Sponsor: niversität Potsdam, Professur für Rehabilitationswissenschaften

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2016-05-11
• Study Completion: 2017-12-21
• Results First Posted: 2019-03-26
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 111

Inclusion Criteria

Implantation of total hip or knee replacement after idiopathic/posttraumatic/congenital osteoarthritis

Exclusion Criteria

No functional safety in walking with full load at the end of inpatient rehabilitation in order to perform progressive exercises with adequate load and measurements at the UP

- Insufficient knowledge of the German language (spoken and written)

Technical exclusion criteria
- No HDMI compatible TV (flat screen TV)
- Less than 2.5 m in front of the screen
- No internet connection (wireless or Ethernet)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Difference in exercise capacity (6-minute walk test [m]) between end and start of intervention

Secondary Outcome Measures

Name	Time	Method
Difference in walking speed (electro-optical passive marker system), functional mobility (Timed Up and Go, Chair Rise and Stair Ascend test), postural control (one-leg stand on a force plate), quality of life and pain (questionnaires SF36 and WOMAC) between intervention end and -beginn and rate of return to work.