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Validity, reliability and responsiveness of the German version of MOXFQ/SEFAS/HOOS

Validity, reliability and responsiveness of the German version of MOXFQ/SEFAS/HOOS

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00007585
Enrollment
300
Registered
2017-10-27
Start date
2015-01-01
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

i.a. Hallux valgus coxarthrosis M20 M16

Interventions

Group 1: Determination of reliability, validity and responsiveness by questioning the participants three times: t1: 3-5 days before the planned surgery
t2: on day of surgery
t3: 5-6 months after surgery. Patients with planned foot and ankle surgery: t1: MOXFQ, SEFAS t2: MOXFQ, SEFAS, SF-36, NRS, FAOS t3: MOXFQ, SEFAS Patients with planned hip surgery: t1: HOOS t2: HOO

Sponsors

LVR-Klinik für Orthopädie Viersen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: MOXFQ/SEFAS: panned foot or ankle surgery, majority HOOS: planned hip surgery, majority

Exclusion criteria

Exclusion criteria: minority, incomprehension of german language

Design outcomes

Primary

MeasureTime frame
Criteria for primary outcome: - determination of reliability via chronbachs alpha and intraclass correlation coefficient (ICC) - determination of criteria- and constructvalidity with spearman non-parametric correlation - the determination of Floor and Ceiling effects - determination of responsiveness via Effect Size (ES), Standardized response mean (SRM) - determination of Minimal important change: Minimal clinical difference (MDC), Standard error of measurement (SEM)

Countries

Germany

Contacts

Public ContactDariusch Arbab

LVR-Klinik für Orthopädie Viersen

darbab@gmx.de02162 9660

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 26, 2026