ENDOprosthetic joint replacement – improving treatment by integrating Prehabilitation, Rehabilitation, Individualized Management and Education

ENDOprosthetic joint replacement – improving treatment by integrating Prehabilitation, Rehabilitation, Individualized Management and Education - EndoPRIME

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

DRKS

Registry ID

DRKS00013521

Enrollment

Registered

2018-01-15

Start date

2015-04-25

Completion date

Unknown

Last updated

2026-08-03

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

Conditions

M16.0 M17.0

Interventions

Group 1: Targeted risk assessment by means of a structured musculoskeletal examination preoperatively - Short Physical Performance Battery (SPPB) - Handheld Dynamometry - Gait Speed - Osteoporosis Ris

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult males and females (age = 18 years) Established diagnosis of Osteoarthritis of the hip, knee or shoulder Given medical indication for total joint replacement.

Exclusion criteria

Exclusion criteria: Acute (< 3 months) or non-consolidated fractures; Planed implantation of a custom-made prosthesis

Design outcomes

Primary

Measure	Time frame
Intraindividual development of osteoarthritis-associated health-limitations as measured by the WOMAC-Score before and 3/6/12 months after surgery	—

Secondary

Measure	Time frame
- Patient Reported Outcome, quantified by standardized questionaires - Type and frequency of perioperative untoward events - Improvement of quality of life in everyday life (EuroQol, PID, LEFS, IPAQ, VAS, CES-D) - Improvement of strength and flexibility/mobility (Chair-Rising-Test, 6-Minute Walk Test, Gait Speed, Short Physical Performance Battery) - Grip strength with dynamometer - Ground reaction force measurement (Leonardo plate) - Body composition (Bioimpedance Analysis) - Satisfaction with artificial joint	—

Measure

Time frame

- Patient Reported Outcome, quantified by standardized questionaires - Type and frequency of perioperative untoward events - Improvement of quality of life in everyday life (EuroQol, PID, LEFS, IPAQ, VAS, CES-D) - Improvement of strength and flexibility/mobility (Chair-Rising-Test, 6-Minute Walk Test, Gait Speed, Short Physical Performance Battery) - Grip strength with dynamometer - Ground reaction force measurement (Leonardo plate) - Body composition (Bioimpedance Analysis) - Satisfaction with artificial joint

—

Countries

Germany

Contacts

Public ContactSilke Achtziger

König-Ludwig-Haus

s-achtziger.klh@uni-wuerzburg.de09318033577

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026