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Quality assurance with cross-sectoral routine data of the health insurance in the orthopedic rehabilitation

Quality assurance with cross-sectoral routine data of the health insurance in the orthopedic rehabilitation - SEQUAR

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00028747
Enrollment
600
Registered
2022-08-10
Start date
2022-11-14
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Patients after total hip or knee replacement surgery

Interventions

Group 1: In the study, data from questionnaires are collected from the patients at 4 measurement points. At the beginning of rehabilitation, at the end of rehabilitation, 3 and 6 months after rehabili

Sponsors

Uniklinik Freiburg; Institut für Medizinische Biometrie und Statistik (IMBI); Sektion Versorgungsforschung und Rehabilitationsforschung (SEVERA)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: • AOK-Insured • undergoing follow-up rehabilitation after total hip or knee joint replacement in a AOK-supported reha-clinic • who have given their consent and • have sufficient German language skills to complete questionnaires in German • Patients over the age of 18

Exclusion criteria

Exclusion criteria: Change of health insurer; Termination of rehab

Design outcomes

Primary

MeasureTime frame
600 patients at 10 rehabilitation facilities are surveyed at four measurement points - at the beginning of rehabilitation, at the end of rehabilitation, 3 and 6 months after rehabilitation. On the patient side, data on [a] daily activities, [b] mobility, [c] physical functioning, [d] emotional status, [e] general pain burden and [f] muscle and joint pain are collected using the following instruments: - Short Musculoskeletal Function Assessment Questionnaire (SFMA-D) [a, b, c, d]. - Indicators of Rehabilitation Status (IRES): Pain scales [e]. - IRES: Mobility scale [b] - IRES: Activities of daily living [a] - IRES: Musculoskeletal Symptoms Scale [f]. Furthermore, data on the general health status (IRES: dimension mental well-being, coping with illness, social integration; scale symptoms cardiovascular) and socio-demography are recorded as potential confounding factors. In addition, medical assessments are carried out at the beginning and end of rehabilitation: Data on the [g] walking ability and, depending on the indication, [h] hip-specific (e.g. limping, stair climbing, walking aids) or [i] knee-specific outcome aspects (e.g. mobility, stability) are collected using the following instruments: - 6-minute walk test [g] - Harris Hip Score [h] - Knee-Society-Score [i]

Secondary

MeasureTime frame
For the retrospective cohort study, the following insured-related routine data of the statutory health insurance will be included: - insurants' master data (§ 288 SGB V) - data from hospital treatment (§ 301 SGB V) - data from inpatient medical rehabilitation (§ 301 SGB V) - data from reimbursed drug treatment (§ 300 SGB V), - data from outpatient treatment (§ 295 SGB V) - data on therapeutic products (§ 302 SGB V) - prescriptions for therapeutic products (§ 302 SGB V) and - nursing services (§ 105 SGB XI)

Countries

Germany

Contacts

Public ContactVanessa Kaiser

UNIVERSITÄTSKLINIKUM FREIBURG; Institut für Medizinische Biometrie und Statistik; Sektion Versorgungsforschung und Rehabilitationsforschung (SEVERA)

bemb.SEQUAR@uniklinik-freiburg.de076120374294

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 10, 2026