Fast track rehabilitation after reversed total shoulder arthroplasty

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON25527

Enrollment

Registered

2019-04-11

Start date

2019-04-01

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

shoulder complaints based on omarthrosis, rotator cuff arthropathy, avascular necrosis and (late) post traumatic

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: • 50 years and older • Selected for rTSA surgery • Complete understandig of the study and signed informed consent

Exclusion criteria

Exclusion criteria: • Selected for rTSA with the indication of fracture treatment after an acute trauma • Individuals who are unable to follow an intense mobilization program. • Individuals who are unable to complete the PROMs questionnaires.

Design outcomes

Primary

Measure	Time frame
The primary study parameter is the difference in Oxford Shoulder Score (OSS) from preoperative to 6 weeks postoperative.	—

Secondary

Measure	Time frame
Secondary study parameters are: 1. Difference in (ROM), VAS pain scores in rest and during activity and the quality of life (EQ-5D) from preoperative to 6 weeks postoperative. 2. Difference in OSS, (ROM), VAS pain scores in rest and during activity and the quality of life (EQ-5D) from preoperative to 3 months postoperative 3. Difference in OSS, (ROM), VAS pain scores in rest and during activity and the quality of life (EQ-5D) from preoperative to 1 year postoperative 4. Complications and re-admissions until 1 year postoperative. 5. Society costs including healthcare costs, patient and family costs and lost productivity costs.	—

Measure

Time frame

Secondary study parameters are: 1. Difference in (ROM), VAS pain scores in rest and during activity and the quality of life (EQ-5D) from preoperative to 6 weeks postoperative. 2. Difference in OSS, (ROM), VAS pain scores in rest and during activity and the quality of life (EQ-5D) from preoperative to 3 months postoperative 3. Difference in OSS, (ROM), VAS pain scores in rest and during activity and the quality of life (EQ-5D) from preoperative to 1 year postoperative 4. Complications and re-admissions until 1 year postoperative. 5. Society costs including healthcare costs, patient and family costs and lost productivity costs.

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Contacts

Public ContactLieke de Vries

Dijklander Hospital

l.m.a.devries@westfriesgasthuis.nl0229855562

Outcome results