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Quality of Life and Patient Satisfaction after rehabilitation with an orthopaedic knee scooter - a randomised, controlled Multicenter trial

Quality of Life and Patient Satisfaction after rehabilitation with an orthopaedic knee scooter - a randomised, controlled Multicenter trial - Quality of Life after rehabilitation with an orthopaedic knee scooter

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
DRKS
Registry ID
DRKS00032980
Enrollment
100
Registered
2023-11-07
Start date
2021-04-28
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Injury or disease of the lower extremity with the need for partial or complete non-weight bearing Postoperative need for partial or complete non-weight bearing of the lower extremity

Interventions

Group 1: forearm crutches Group 2: forearm crutches and additionally an orthopaedic knee scooter

Sponsors

Klinik für Orthopädie und Unfallchirurgie, Muskuloskelettales Universitätszentrum München (MUM), LMU Klinikum, LMU München
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Illnesses, injuries or operations of the foot, ankle or distal lower leg with a required partial loading or unloading phase of several weeks for the respective affected extremity.

Exclusion criteria

Exclusion criteria: - Impairment of both lower extremities - Pregnancy/breastfeeding - Impairment of the upper extremity that makes the use of forearm crutches or the Forearm crutches or the orthopedic scooter. - Lower extremity weight-bearing impairment, such as immobilized knee joint arthroplasty (which precludes the use of forearm crutches or an orthopedic scooter). - Balance disorders that contraindicate the use of an orthopedic scooter or forearm crutches - Thrombosis or high-grade arteriovenous disorders of the affected extremity. - Legal care

Design outcomes

Primary

MeasureTime frame
Patient satisfaction, quality of life, walking distance according to SF-36, EQ5D and custom made questionnaire after the end of the use of the aids.

Secondary

MeasureTime frame
mobility, medical leave according to SF-36, EQ5D and custom made questionnaire after the end of the use of the aids.

Countries

Germany

Contacts

Public ContactChristian Ehrnthaller

Klinik für Orthopädie und Unfallchirurgie, Muskuloskelettales Universitätszentrum München (MUM), LMU Klinikum, LMU München

christian.ehrnthaller@med.uni-muenchen.de+49891776031980

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 6, 2026