SpondyloarthritisNCT04369651
Socio-economic Determinants for Acceptance and Choice of Biological Treatment
An observational study of Spondyloarthritis, run by National Center for Rheumatic Diseases, Nepal.
Trial summary
This was a cross-sectional study conducted at National center for rheumatic diseases, Nepal on SpA patient refractory to initial treatment with conventional anti rheumatic drugs. Patients taking TNFi (tumor necrosis factor inhibitor- adalimumab or etanercept) or tofacitinib were included. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Spondyloarthritis
- How many people
- 117 participants
- Where
- No sites listed yet
- Study dates
- 1 Jun 2015to 31 Dec 2019
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patients with SpA and enrolled in the cohort database from June 2015 to December 2019 were selected.
Who may be able to join
- patients with spondyloarthropathy
- on any oral or injectable forms of biological treatment
Who cannot join
- less than 18years of age
- who did not consent for participation
- deferred from biological treatment due to comorbid conditions like concurrent infections or heart failure
About this study
Official title: Socio-economic Determinants for Acceptance and Choice of Biological Treatment by Patients With Spondyloarthropathy in Nepal
This was a cross-sectional study conducted at National center for rheumatic diseases, Nepal on SpA patient refractory to initial treatment with conventional anti rheumatic drugs. Patients taking TNFi (tumor necrosis factor inhibitor- adalimumab or etanercept) or tofacitinib were included. Baseline demographic, socio-economic, clinical data were recorded.
Read the detailed description
This was a cross-sectional observational study conducted in the rheumatology clinic of National Center for Rheumatic Diseases, Kathmandu, Nepal. Patients with spondyloarthropathy (SpA) and enrolled in the cohort database from June 2015 to December 2019 were selected. Those taking any oral or injectable forms of biological treatment were included in the study. Patients less than 18 years of age, who did not consent for participation or additional information, who were deferred from biological treatment due to comorbid conditions like concurrent infections or heart failure were excluded. An informed consent was obtained from selected patients and any additional information required was taken via e-mail or telephone enquiry.
Diagnostic \& measurement tools Diagnosis of SpA was made by rheumatologists on the basis of the modified New York Criteria for Ankylosing Spondylitis and the ASAS criteria (Assessment of SpondyloArthritis International Society) for axial and peripheral SpA. Diagnosis of nr-axial SpA was made by MRI evidence of sacroilitis in a patient with normal radiograph with or without HLA B27. Disease activity was assessed using composite Ankylosing Spondylitis Disease Activity Score (ASDAS) and the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI).
Socioeconomic status Socioeconomic factors studied were educational level and the primary occupation. Patient self-reported highest educational level was recorded and was categorized into illiterate, primary, secondary, higher secondary, above secondary level education. Occupation and social class were recorded based on self-report primary source of income. It was categorized into homemakers, students, service holders, business, teachers, farmers and others (field workers, labor workers). A dedicated research officer also took data on other demographic parameters and geographical location of residence. Geographical location was categorized into urban-rural and hilly-plain terrain.
Indications for offering biological treatment Indications for biological or small molecule treatment included: a. Failure of at least 2 courses of NSAIDS, b. Failure of at least 3months of conventional synthetic DMARDs (csDMARDs). For patients with PsA, the csDMARDs included methotrexate and/or leflunomide; for AS, nr-axial SpA and IBD-associated arthritis, it included sulfasalazine and/or methotrexate. Failure of treatment was defined as: a. Persistent ASDAS of ≥2.1, b. Improvement of ASDAS by less than -1.1, c. Persistent BASDAI of ≥4. All patients fulfilling these indications were offered biological treatment. Patients with no contraindication for TNFi were offered either injectable biologicals (adalimumab or etanercept: only TNFi available in Nepal) or tofacitinib (only small molecule available in Nepal) and explained about the preparatory investigations, dosage of TNFi, storage, cost, monitoring and side-effects.
Data collection and analysis Complete data on baseline demographic parameters (age, gender, address, education, occupation) and ASDAS and BASDAI scores at initiation of treatment with biological or small molecule were recorded in a hardcopy data-sheet and later entered to a predesigned excel-sheet by a trained research officer.
Statistical analysis was performed using SPSS version 21 (IBM Corp, USA). Simple descriptive statistics were used to analyze various socioeconomic and demographic parameters. Chi-squared test was used to analyze difference in these parameters between patients who chose injectable and those who chose tofacitinib. Linear regression analysis was performed to identify variables associated with use of any biological agent. All variables with p-value of <0.05 were analyzed in multiple regression model to evaluate the independent association. Difference in mean values between two treatment groups were assessed by independent t-test.
- Conditions
- Spondyloarthritis
- Keywords
- socio-economic determinants, biologic, Nepal, low income country, spondyloarthroathy
- Medical subject headings
- Spondylarthritis
What is being measured
The primary outcome is the main question the study is designed to answer.
socio economic determinants
socio economic determinants for acceptance of biologic therapy
Measured: four years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Apr 2020
- Study start1 Jun 2015
- Primary completion31 Dec 2019
- Study completion31 Dec 2019
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for SpondyloarthritisStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 117 participants (actual)
Sponsor and investigators
- Lead sponsor
- National Center for Rheumatic Diseases, Nepal
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Shweta Nakarmi, National Center for Rheumatic Diseases, Nepal
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04369651
- Sponsor's protocol ID
- 210/2017
- Status last verified
- Apr 2020
- First submitted
- 28 Apr 2020
- Last updated
- 1 May 2020
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 1 May 2020. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Socio-economic Determinants for Acceptance and Choice of Biological Treatment by Patients With Spondyloarthropathy in Nepal
- ClinicalTrials.gov ID
- NCT04369651
- Acronym / sponsor ID
- 210/2017
- Conditions
- Spondyloarthritis
- Keywords
- socio-economic determinants, biologic, Nepal, low income country, spondyloarthroathy
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 117 participants (actual)
- Lead sponsor
- National Center for Rheumatic Diseases, NepalUniversity, hospital or other
- Study start
- 1 Jun 2015 (actual)
- Primary completion
- 31 Dec 2019 (actual)
- Study completion
- 31 Dec 2019 (actual)
- First posted
- 30 Apr 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This was a cross-sectional study conducted at National center for rheumatic diseases, Nepal on SpA patient refractory to initial treatment with conventional anti rheumatic drugs. Patients taking TNFi (tumor necrosis factor inhibitor- adalimumab or etanercept) or tofacitinib were included. Baseline demographic, socio-economic, clinical data were recorded.
Detailed description
This was a cross-sectional observational study conducted in the rheumatology clinic of National Center for Rheumatic Diseases, Kathmandu, Nepal. Patients with spondyloarthropathy (SpA) and enrolled in the cohort database from June 2015 to December 2019 were selected. Those taking any oral or injectable forms of biological treatment were included in the study. Patients less than 18 years of age, who did not consent for participation or additional information, who were deferred from biological treatment due to comorbid conditions like concurrent infections or heart failure were excluded. An informed consent was obtained from selected patients and any additional information required was taken via e-mail or telephone enquiry.
Diagnostic \& measurement tools Diagnosis of SpA was made by rheumatologists on the basis of the modified New York Criteria for Ankylosing Spondylitis and the ASAS criteria (Assessment of SpondyloArthritis International Society) for axial and peripheral SpA. Diagnosis of nr-axial SpA was made by MRI evidence of sacroilitis in a patient with normal radiograph with or without HLA B27. Disease activity was assessed using composite Ankylosing Spondylitis Disease Activity Score (ASDAS) and the Bath Ankylosing Spondylitis Disease Activity Index (BASDAI).
Socioeconomic status Socioeconomic factors studied were educational level and the primary occupation. Patient self-reported highest educational level was recorded and was categorized into illiterate, primary, secondary, higher secondary, above secondary level education. Occupation and social class were recorded based on self-report primary source of income. It was categorized into homemakers, students, service holders, business, teachers, farmers and others (field workers, labor workers). A dedicated research officer also took data on other demographic parameters and geographical location of residence. Geographical location was categorized into urban-rural and hilly-plain terrain.
Indications for offering biological treatment Indications for biological or small molecule treatment included: a. Failure of at least 2 courses of NSAIDS, b. Failure of at least 3months of conventional synthetic DMARDs (csDMARDs). For patients with PsA, the csDMARDs included methotrexate and/or leflunomide; for AS, nr-axial SpA and IBD-associated arthritis, it included sulfasalazine and/or methotrexate. Failure of treatment was defined as: a. Persistent ASDAS of ≥2.1, b. Improvement of ASDAS by less than -1.1, c. Persistent BASDAI of ≥4. All patients fulfilling these indications were offered biological treatment. Patients with no contraindication for TNFi were offered either injectable biologicals (adalimumab or etanercept: only TNFi available in Nepal) or tofacitinib (only small molecule available in Nepal) and explained about the preparatory investigations, dosage of TNFi, storage, cost, monitoring and side-effects.
Data collection and analysis Complete data on baseline demographic parameters (age, gender, address, education, occupation) and ASDAS and BASDAI scores at initiation of treatment with biological or small molecule were recorded in a hardcopy data-sheet and later entered to a predesigned excel-sheet by a trained research officer.
Statistical analysis was performed using SPSS version 21 (IBM Corp, USA). Simple descriptive statistics were used to analyze various socioeconomic and demographic parameters. Chi-squared test was used to analyze difference in these parameters between patients who chose injectable and those who chose tofacitinib. Linear regression analysis was performed to identify variables associated with use of any biological agent. All variables with p-value of <0.05 were analyzed in multiple regression model to evaluate the independent association. Difference in mean values between two treatment groups were assessed by independent t-test.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients with SpA and enrolled in the cohort database from June 2015 to December 2019 were selected.
Key inclusion criteria (2 listed)
- patients with spondyloarthropathy
- on any oral or injectable forms of biological treatment
Key exclusion criteria (3 listed)
- less than 18years of age
- who did not consent for participation
- deferred from biological treatment due to comorbid conditions like concurrent infections or heart failure
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
socio economic determinants
Time frame: four years
socio economic determinants for acceptance of biologic therapy
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 1 May 2020.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
An observational study of Spondyloarthritis, run by National Center for Rheumatic Diseases, Nepal.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 1 May 2020. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
socio economic determinants (time frame: four years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 May 2020.