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Behçet's Disease Overall Damage Index (BODI)

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ClinicalTrials.gov Identifier: NCT03803462
Recruitment Status : Recruiting
First Posted : January 14, 2019
Last Update Posted : January 15, 2019
Sponsor:
Information provided by (Responsible Party):
Matteo Piga, University of Cagliari

Tracking Information
First Submitted Date January 10, 2019
First Posted Date January 14, 2019
Last Update Posted Date January 15, 2019
Actual Study Start Date August 1, 2017
Estimated Primary Completion Date June 2019   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: January 13, 2019)
Behçet's disease Overall Damage Index [ Time Frame: Baseline ]
Prevalence and type of organ damage in Behçet's Disease assessed by experimental tool
Original Primary Outcome Measures
 (submitted: January 10, 2019)
Behçet's disease Overall Damage Index [ Time Frame: At a single time-point ]
Prevalence and type of organ damage in Behçet's Disease assessed by experimental tool
Change History Complete list of historical versions of study NCT03803462 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures
 (submitted: January 13, 2019)
  • Vasculitis Damage Index [ Time Frame: Baseline ]
    Prevalence and type of organ damage in Behçet's Disease assessed by non specific tool different
  • Disease activity (Behçet disease actvity form) [ Time Frame: Baseline ]
    Prevalence and level of disease activity
  • Health Related Quality of Life (HRQoL) [ Time Frame: Baseline ]
    Health Related Quality of Life measured by the eight scaled scores of the SF-36: 1) vitality; 2) physical functioning; 3) bodily pain; 4) general health perceptions; 5) physical role functioning; 6) emotional role functioning; 7) social role functioning; 8) mental health. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability
Original Secondary Outcome Measures
 (submitted: January 10, 2019)
  • Vasculitis Damage Index [ Time Frame: At a single time-point ]
    Prevalence and type of organ damage in Behçet's Disease assessed by non specific tool different
  • Disease activity (Behçet disease actvity form) [ Time Frame: At a single time-point ]
    Prevalence and level of disease activity
  • Health Related Quality of Life (HRQoL) [ Time Frame: At a single time-point ]
    Health Related Quality of Life measured by SF-36
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title Behçet's Disease Overall Damage Index
Official Title Development and Preliminary Validation of the Behçet's Disease Overall Damage Index
Brief Summary

Damage in vasculitis, as well as in other chronic inflammatory disorders, accrues over time resulting in impairment of quality of life, development of disability and increased mortality. For these reasons, damage represents an important outcome to be assessed and measured both in trials and clinical practice.

Currently, the most widely used assessment tool for damage in vasculitis is the Vasculitis Damage Index (VDI). However, VDI was developed for a no specific type of vasculitis and it appears to be more suitable for damage assessment in ANCA-associated vasculitis than in Behçet' disease (BD).

BD is a chronic and multisystem inflammatory disorder classified among vasculitides. As well as in other vasculitides, disease activity and treatment in BD can result in the development and accumulation of irreversible organ damage, such as blindness, tissue loss and a wide range of neurologic disorders. Recently the OMERACT has defined the Core Set domain of Outcome Measures for BD. Despite damage is included in the OMERACT outcome core set for rheumatic disease, a specific assessment tool for BD is currently not available.

The aim of this study is to develop and validate the first tool for describing and measuring organ damage in patients with Behçet Disease (Behçet's disease Overall Damage index - BODI).

Detailed Description

DESIGN OF THE STUDY

This observational multicenter study will be developed in 2 subsequent phases, in their turn, consisting of different steps (figure 1):

  1. BODI Development 1.1) Development of a preliminary version of BODI (p-BODI) based on literature review and inspired by pre-existing tools according to OMERACT guidelines; 1.2) Delphi process aimed to review and improve the p-BODI.
  2. Validation of the new tool according to OMERACT filter 2.0 2.1) Application of the BODI on a multicentre cohort of BD patients. 2.2) Assessment of face, content, construct and criterion validity, and sensitivity to change.

2.3) Assessment of reliability based on scoring exercise on clinical vignettes.

All subjects involved in the study are experts in the management of BD. They will work in two different groups having different roles:

  • Work and facilitator group (WFG): consisting of 3 Physician from the Coordinating Centre. The tasks of the WFG are: (a) to review literature and develop a preliminary version of BODI (p-BODI), including: definition of damage, rules for scoring and identification of potential items of damage; (b) to coordinate the Delphi process for editing and optimizing p-BODI; (c) to analyse data from the validation process.
  • Expert Panel (EP): consisting of multidisciplinary experts in Behçet's disease and Patient's delegate from different countries. EP members will be selected and invited to participate in the study by the WFG. The tasks of the EP are to express their opinion on p-BODI and propose editing for its improvement within a Delphi process;
  • Clinicians group (CG): consisting of one Clinician from each Centre, with expertise in Behçet's disease but not involved in the Delphi process. The tasks of this group are: (a) to apply the BODI on 30 consecutive patients with BD (10 for Neurologist and Ophthalmologist) from each Centre involved in the study; (b) to score a set of clinical vignettes using the BODI, to assess reliability of the instrument; (c) to express an overall judgement (in an online survey) regarding to general credibility, comprehensiveness and feasibility of the BODI.

The member of EP and GC, involved in the study so far, with respective affiliations, are reported below:

EP members - CG members - Affiliations.

  • Prof. Alessandro Mathieu - Dr. Matteo Piga - Chair and Unit of Rheumatology, University and AOU of Cagliari, Monserrato - Italy;
  • Prof. Govoni Marcello - Dr. Lo Monaco Andrea - Department of Medical Sciences, Section of Rheumatology, AOU S. Anna, the University of Ferrara - Italy;
  • Prof. Iannone Florenzo - Dr. Lopalco Giuseppe - Department of Emergency and Organ Transplantation, Rheumatology Unit, University of Bari - Italy;
  • Prof. Neri Piergiorgio - Dr. Pirani Vittorio - Ocular Immunology Service, the Eye Clinic, Polytechnic University of Marche- Ancona - Italy;
  • Prof. Cantarini Luca - Dr. Orlando Ida - Rheumatology Unit, University of Siena. Policlinico Le Scotte;
  • Prof. Martins Silva Ana - Dr. Santos Ernestina - Neurology Department, Hospital Santo António, Centro Hospitalar do Porto - Portugal;
  • Prof. Vasconcelos Carlos - Prof Correia Joao; Dr. Raquel Faria - Clinical Immunology Unit, Centro Hospitalar do Porto and UMIB, ICBAS, Universidade do Porto, Portugal;
  • Prof. Cervera Ricard - Dr. Espinosa Gerard, Dr. Ignasi Rodriguez - Department of Autoimmune Diseases, Hospital Clinic, IDIBAPS, University of Barcelona - Spain;
  • Prof. Bertsias George - Dr. Nikos Kougkas - Department of Rheumatology, Clinical Immunology and Allergy, University of Crete School of Medicine - Grece;
  • Patient Association delegates.

OPERATIVE STUDY DEVELOPMENT AND DATA ANALYSIS

  1. BODI Development 1.1) Development of preliminary version of BODI (p-BODI) based on literature review and inspired to pre-existing tools A preliminary list of damaged items with respective definition will be generated after reviewing the literature and preexisting damage indices (e.g VDI for vasculitides and SLICC damage index (SDI) for systemic lupus erythematosus).

    1.2) Reviewing and editing of the p-BODI by Delphi process A multi-step Delphi process, based on reaching experts consensus, will be performed in order to review and refine the p-BODI and the respective glossary. Through an online survey, each member EP will be asked to rate: (a) how strongly they agree with the general rules for damage scoring; (b) how strongly they agree to include the listed damage items within the BODI (e.g. to which extent do you agree that "Cataract" should be included in the BODI?); (c) how strongly they agree with the provided item definition. Ratings will be scored on a 5-point Likert scale (5 = strongly agree; 4 = agree; 3 = unsure; 2 = disagree; 1 = strongly disagree). The EP members will be asked to give considerations and arguments to support their opinion, especially if they score less than 4. They will also be given the opportunity to suggest alternative wordings, to suggest additional items, or to make any other comment.

    In the reviewed p-BODI for the subsequent Delphi round, each issue (scoring rules, damage items, item definitions) if: (a) ≥80% of EP members scores ≥4: will be included; (b) 50-79% of EP members scores ≥4: will be included in the second questionnaire after reviewing according to comments and suggestions provided in the previous round (c) <50% of EP members scores: will be excluded.

    The WFG has the right to make alternative decisions after reviewing the EP responses (e.g propose to change an item definition according to a suggestion from the expert panel, even if the item was scored >4 by ≥80% of EP).

    An anonymous feedback report will be provided with the second questionnaire, in order to offer the opportunity to reconsider and, if appropriate, to change a previous opinion in light of the anonymous responses and considerations of the other EP members. The panel members will again be asked to give their opinion on each issue in subsequent rounds until complete consensus will be achieved (all issues scored ≥4 by ≥80% of EP) and the definitive version of BODI will be developed.

  2. Validation of BODI 2.1) Application of BODI on a multi-center cohort of BD patients Each CG member will be asked to apply the reviewed version of BODI on a cohort of 30 BD patients consecutively assessed in their own center. For Neurologist and Ophthalmologist, the data from 10 consecutive patients will be enough. This is because Neurologist and Ophthalmologist usually take care of the most severe neuropsychiatric and ocular cases, which might bias the real prevalence of these manifestations in the study cohort.

A multicenter cohort consisting of 200-250 BD patients will be thus set up. Patients will undergo a routine clinical assessment, as scheduled in their follow-up program. No further clinical, laboratory or instrumental investigations will be performed in addition to those provided according to the good clinical practice. Any possible drug administration will be evaluated independently from the study and according to the good clinical practice.

Inclusion criteria will be: a) BD diagnosis according to ICBD criteria, b) disease duration ≥12 months), c) age at enrolment ≥ 18 years. For each recruited patient data will be anonymously collected at the enrolment visit (T0). For patients with more than 5 years of follow-up at the enrollment time, investigators will be further asked to perform a 5 years retrospective BODI (Tr5). The following data will be collected (see the attached Case Report Form):

- T1: demographics and medical history (gender; birthday, onset, diagnosis and enrolment date; country of origin; ethnicity; comorbidity; smoker status); cumulative clinical manifestation from onset to enrolment (oral aphthosis, genital aphthosis, skin lesions, ocular involvement, neurologic lesions, vascular lesions, pathergy test, arthritis, gastrointestinal manifestations); active clinical manifestations the enrolment visit; ongoing and past therapy; BD current activity form (BDCAF); BODI; VDI; Physician global assessment (PGA)on visual analogic scale; Patients global assessment (PtGA) on visual analogic scale; Short Form 36 (SF-36) Health Survey,

• Tr5 (retrospectively): BODI

2.2) Assessment of face, content, construct, criterion validity and sensitivity to change Validation will be performed according to the principles of OMERACT Filter 2.0, thus according to the criteria of (A) truth, (B) discrimination and (C) feasibility will be assessed.

A.1. Face validity. Since BODI will be developed through literature review and consensus between an expert in BD management, face validity criteria should be automatically met. However, face validity will be further tested by asking each CG member to complete a questionnaire investigating the suitability of the tool.

A.2. Content validity. To assure content validity, the presence of damage identified by CG but not classifiable in BODI will be assessed. Content validity will be further tested by asking each CG member to complete a questionnaire relating to the comprehensiveness of the instrument.

A.3. Construct validity. It will be assessed analyzing the agreement between results of damage assessment on our validation cohort by BODI and other damage assessment tool. Since there are no other specific and validate instruments for damage amassment in Behçet disease, SLICC and VDI will be used as a surrogate. Correlation between the different indices results will be evaluated by Pearson's or Spearman's correlation coefficients.

A.4. Criterion Validity. Criterion validity represents the correlation with results of measurement with the new tool and other long-term outcomes related to the phenomenon we are measuring. Since we expect that damage correlates with quality of life, disability and mortality, a correlation between BODI score and SF-36, HAQ and in the future also with mortality rate will be assessed.

B.1. Reliability. Clinical vignettes will be created from real cases to test the reliability of the BODI. Thus, inter-observer agreement (kappa) will be assessed by asking a physician from every center to assess the same clinical vignettes.

B.2. Sensitivity to change. The ability of the BODI to record the accumulation of damage over time will be examined by determining the change in BODI score over 5 years of follow-up on the validation cohort. The average increase of BODI score from T1 to T2 will be calculated and will be tested by the Mann-Whitney test.

C. Feasibility. To test feasibility each CG member will be asked to complete a questionnaire relating to the ease of use, consumption of time and interpretability of the instrument.

Study Type Observational
Study Design Observational Model: Cohort
Time Perspective: Cross-Sectional
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population A multicenter cohort consisting of 200-250 consecutive BD patients. Each participating investigator will enroll a cohort of 20-30 BD patients consecutively assessed in its own center.
Condition
  • Behçet Disease
  • Behcet's Disease Aggravated
Intervention Other: Behçet's disease Overall Damage Index (BODI)
BODI is a tool to document any organ damage that has occurred in patients since the onset of BD. It includes a form and an associated glossary with the definition of the items.
Study Groups/Cohorts Not Provided
Publications *

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Recruiting
Estimated Enrollment
 (submitted: January 10, 2019)
210
Original Estimated Enrollment Same as current
Estimated Study Completion Date December 2019
Estimated Primary Completion Date June 2019   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

  • BD diagnosis according to ICBD criteria;
  • disease duration ≥12 months;
  • age at enrolment ≥ 18 years;
  • Able to understand and voluntarily sign informed consent forms (ICFs) prior to the initiation of any study-specific assessments/procedures.

Exclusion Criteria:

  • unable to adhere to the protocol requirements.
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts
Contact: Matteo Piga, MD +390706754069 matteopiga@unica.it
Contact: Alberto Floris, MD +3907051093348 albertofloris1@gmail.com
Listed Location Countries Greece,   Italy,   Portugal,   Spain,   United Arab Emirates
Removed Location Countries  
 
Administrative Information
NCT Number NCT03803462
Other Study ID Numbers BODI
Has Data Monitoring Committee No
U.S. FDA-regulated Product
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
IPD Sharing Statement
Plan to Share IPD: Yes
Plan Description: De-identified individual participant data for all outcome measures will be made available.
Supporting Materials: Study Protocol
Supporting Materials: Statistical Analysis Plan (SAP)
Supporting Materials: Informed Consent Form (ICF)
Supporting Materials: Clinical Study Report (CSR)
Time Frame: .Within 6 months of study completion.
Access Criteria: Upon request
Responsible Party Matteo Piga, University of Cagliari
Study Sponsor University of Cagliari
Collaborators Not Provided
Investigators
Principal Investigator: Matteo Piga, MD Azienda Ospedaliero Universitaria Cagliari
PRS Account University of Cagliari
Verification Date January 2019