FAIWHC: Italian Translation and Transcultural Validation of Frenchay Activity Index and Walking Handicap Classification in Stroke

Sponsor
Fondazione Don Carlo Gnocchi Onlus (Other)
Overall Status
Unknown status
CT.gov ID
NCT04285957
Collaborator
(none)
70
1
14
5

Study Details

Study Description

Brief Summary

This study is aimed at providing an Italian version of two assessment tools for participation in stroke patients, the Frenchay Activity Index (FAI) and the Walking Handicap Classification (WHC) by a standardized translation and transcultural validation protocol. The protocol includes a pre-test of the Italian version on ten patients, a final revision, and a validation on a sample of 60 stroke patients.

Condition or Disease Intervention/Treatment Phase
  • Other: Questionnaire administration pre test
  • Other: Questionnaire administration - validation

Detailed Description

This study is aimed at providing an Italian version of two tools to assess participation in stroke patients, the Frenchay Activity Index (FAI) and the Walking Handicap Classification (WHC). These tools have been recently indicated for the assessment of participation in Stroke patients by the Italian Association of Physical and Rehabilitation Medicine (Minimal Stroke Assessment Protocol - PMIC2); they are currently used in Italian research and clinical settings, but no official translation exists. The process requires a standardized translation protocol, including forward and backward translation, using a multistep revision structure, to ensure conceptual and semantic equivalence. The validation process includes a pilot evaluation of on 10 individuals post-stroke admitted to the Neurological Rehabilitation Unit, Foundation Don Gnocchi Scientific Institute, and a validation on a sample of 60 stroke patients including reliability, internal consistency and concurrent validity assessment of the translated version against the Sickness Impact Profile (SIP) - Italian version and the Rivermead Mobility Index (RMI) - Italian version, respectively

Study Design

Study Type:
Observational
Anticipated Enrollment :
70 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
Italian Translation and Transcultural Validation of Two Assessment Tools for Participation in Stroke Survivors: the Frenchay Activity Index and the Walking Handicap Classification (FAIWHC)
Anticipated Study Start Date :
Sep 15, 2020
Anticipated Primary Completion Date :
Sep 14, 2021
Anticipated Study Completion Date :
Nov 15, 2021

Arms and Interventions

Arm Intervention/Treatment
pre-test Group

Consecutive recruitment of 10 post-stroke patients undergoing intensive rehabilitation treatment at the Neurological Rehabilitation Unit, Foundation don Gnocchi Scientific Institute. Inclusion criteria: age 18-90, stroke occurred within 3 months from enrollment; clinical stability (SIC = 0). The exclusion criteria are: stroke recurrence; visual and / or hearing disorders; cognitive decline (MMSE <21) and/or severe aphasia, which would limit the the patients' understanding of and the reliable answering to the two assessment tools

Other: Questionnaire administration pre test
Pre-test: Two expert physicians/physical therapist shall be involved in the questionnaire administration (A/B). The questionnaires shall be randomly administered to the patients by one operator at T0 the same test shall be readministered after 1-2 weeks by another operator (T1), blind to the first assessment; the second operator shall also administer the additional measures (SIP and RMI);
Other Names:
  • Questionnaire administration - validation
  • Validation Group

    Recruitment of 60 post-stroke patients undergoing intensive rehabilitation treatment at the Neurological Rehabilitation Unit, Foundation don Gnocchi Scientific Institute.Inclusion criteria: age 18-90, stroke occurred within 8 months from enrollment; clinical stability (SIC = 0). If the following criteria are present: visual and / or hearing disorders; cognitive decline (MMSE <21) and/or severe aphasia, which would limit the patients' understanding of and the reliable answering to the two assessment tools, the interview shall be carried out with a proxy

    Other: Questionnaire administration - validation
    Validation Two expert physicians shall be involved in the questionnaire administration (A/B). The questionnaires shall be randomly administered to the patients by one operator at T0 the same test shall be readministered after 1-2 weeks by another operator (T1), blind to the first assessment; the second operator shall also administer the additional measures (SIP and RMI); In case the patient is unable to be interviewed due to aphasia cognitive or sensorial problems, a proxy would be interviewed both at T0 and at T1 (the same proxy would be interviewed both times)

    Outcome Measures

    Primary Outcome Measures

    1. Interrater reliability [1 year]

      Intraclass Correlation Coefficient >=0,70

    2. Internal consistency (FAI) [1 year]

      Cronbach's alpha>=0,70

    3. concurrent validity of FAI against SIP [1 year]

      Spearman's coefficient >=0.25-0.50

    4. concurrent validity of WHC against RMI [1 year]

      Spearman's coefficient >=0.25-0.50

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No

    Pre-test: consecutive recruitment of 10 post-stroke patients undergoing intensive rehabilitation treatment at the Neurological Rehabilitation Unit, Foundation don Gnocchi Scientific Institute.

    Inclusion criteria:
    • age 18-90;

    • stroke occurred within 3 months from enrollment;

    • clinical stability (SIC = 0).

    Exclusion criteria:
    • stroke recurrence;

    • visual and / or hearing disorders;

    • cognitive decline (MMSE <21) and/or severe aphasia, which would limit the the patients' understanding of and the reliable answering to the two assessment tools

    Validation: recruitment of 60 post-stroke patients undergoing intensive rehabilitation treatment at the Neurological Rehabilitation Unit, Foundation don Gnocchi Scientific Institute-

    Inclusion criteria:
    • age 18-90,

    • stroke occurred within 8 months from enrollment;

    • clinical stability (SIC = 0).

    Criteria for carrying out the interview with a proxy. If a proxy is not available, the patient is excluded:

    • visual and / or hearing disorders;

    • cognitive decline (MMSE <21) and/or severe aphasia, which would limit the patients' understanding of and the reliable answering to the two assessment tools.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Fondazione don Gnocchi Florence Italy 50143

    Sponsors and Collaborators

    • Fondazione Don Carlo Gnocchi Onlus

    Investigators

    • Principal Investigator: Francesca Cecchi, Md, Fondazione don Carlo Gnocchi IRCCS

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Fondazione Don Carlo Gnocchi Onlus
    ClinicalTrials.gov Identifier:
    NCT04285957
    Other Study ID Numbers:
    • FAIWHC
    First Posted:
    Feb 26, 2020
    Last Update Posted:
    Aug 28, 2020
    Last Verified:
    Feb 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Fondazione Don Carlo Gnocchi Onlus
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 28, 2020