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Translation and Psychometric Testing of the Norwegian Foot Functional Index Revised, Short Version.

Translation, Cross-culture Adaption of Foot Functional Index Revised, Short Version (FFI-RS) Into Norwegian. Testing of Psychometric Properties.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04207164
Enrollment
139
Registered
2019-12-20
Start date
2018-03-23
Completion date
2021-02-19
Last updated
2022-04-20

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

Conditions

Foot Diseases, Plantar Fascitis

Keywords

Foot Functional Index revised,, Translation and cultural adaption, Reliability, Validity, Responsiveness

Brief summary

The aim of this study is to translate into Norwegian and cross-culturally adapt the Foot Functional Index- revised, short form (FFI-RS) according to international guidelines. Furthermore, the reliability and the validity, responsiveness as well as floor and ceiling effect of the Norwegian version of the FFI-RS will be determined.

Detailed description

Foot Functional Index, revised short form is a foot specific patient reported outcome measurement (PROM) which covers pain, stiffness, activity limitations, disability as well as psychosocial issues. The aim of this study is to translate into Norwegian and cross-culturally adapt Foot Functional Index revised, short form (NFFI-RS). Furthermore, the reliability, validity, interpretability and responsiveness will be determined. The Department of Physical Medicine and Rehabilitation at Oslo University Hospital has an ongoing double blind, randomized sham-controlled trial (RCT) comparing the effect of radial extracorporeal shock wave therapy (rESWT), sham rESWT, standardized exercise program and usual care for patients with longstanding plantar fasciopathy (NCT03472989). The testing of the psychometric properties of the NFFI-RS will include totally hundred patients, both from the mentioned RCT as well as patients with other foot diagnosis recruited from our department. The translation of the original FFI-RS into Norwegian has been done following the official guidelines. In the test-retest study fifty patients will complete the NFFI-RS at a one week interval. Smallest detectable change, measurement error, floor and ceiling effects as well as internal consistency will be calculated by using the baseline data. To decide the construct validity we will test the various hypothesis at baseline. To calculate the responsiveness and the minimal clinically important change three months data will be assessed. Patient Global Impression of Change Scale will be used to assess the minimal clinically important change and responsiveness of the NFFI-RS with ROC and AUC analyses.

Interventions

None listed

Sponsors

Oslo University Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years

Inclusion criteria

* Patients with pain localized in the foot * Patients understanding oral and written Norwegian

Exclusion criteria

* Patients without pain in the foot * Patients not understanding oral and written Norwegian

Design outcomes

Primary

MeasureTime frameDescription
Foot Functional Index revised short version ( FFI-RS)Baseline, 1 week, 3 monthsFFI-RS is a foot specific pain and function score. We will evaluate the reliability of the FFI-RS by testing the internal consistency (Cronbach's Alpha). Furthermore test-retest will be done with a second FFI-RS recording after one week (weighted Kappa). We will evaluate construct validity with other instruments (RAND-12 and NRS). To test the responsiveness of FFI-RS, we will evaluate the change in FFI-RS from baseline to 3 months with Patient Global Impression of Change score.

Secondary

MeasureTime frameDescription
Numeric Rating Scale (NRS)BaselineChange in heel pain (during Activity last week). NRS is a patient reported pain intensity scale ranging from 0 (no pain) to 10 (worst possible pain). NRS will by used for evaluating the construct validity of FFI-RS.
RAND-12BaselineHealth related quality of life (12 items). RAND-12 will be used for evaluating the construct validity of FFI-RS.
Patient Global Impression Of Change Scale (PGIC)3 months7-point scale ranging from very much improved to very much worse. PGIC will be used for evaluating the responsiveness of FFI-RS.

Countries

Norway

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026