PROM Collected Via a WebApp Versus a Touch Screen Solution Among Patients With SLE
Primary Purpose
Systemic Lupus Erythematosus
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
PROM registration via the DANBIO WebApp and the outpatient touchscreen in a randomised order
Sponsored by
About this trial
This is an interventional other trial for Systemic Lupus Erythematosus
Eligibility Criteria
Inclusion Criteria:
- Diagnosed in DANBIO with SLE
- Experience with the PROM questionnaires in DANBIO (≥ 1 previous assessments)
Exclusion Criteria:
- Inability to provide informed consent or to comply with the study protocol
- Diagnosis of SLE of ≥ 12 months
- Does not have access to a device that can run the DANBIO webapp
Sites / Locations
- Department of Rheumatology
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Other
Arm Label
Group WT
Group TW
Arm Description
PROM registration via the DANBIO WebApp and thereafter the outpatient touchscreen
PROM registration via the outpatient touchscreen and thereafter the DANBIO WebApp
Outcomes
Primary Outcome Measures
Change in Systemic Lupus Activity Questionnaire global health
Evaluates global assessment of lupus activity using an NRS score from 0-10. Higher score Means worse outcome.
Secondary Outcome Measures
Change in Health Assessment Questionnaire (HAQ)
Assess the patient's physical function from 0-3. Higher score Means worse outcome.
Visual Analogue Scale for Pain
The patient's assessment of pain on a scale from 0-100 within the last week.The left of the scale (0) signifies the absence of pain and the right end (100) maximum pain.
Visual Analogue Scale for fatigue
The patient's assessment of fatigue on a scale from 0-100 within the last week. The left of the scale (0) signifies the absence of fatigue and the right end (100) maximum fatigue.
Patient Global Visual Analogue Scale
The patient's global assessment of disease activity (arthritis severity) on a scale from 0-100 within the last week. The left of the scale (0) signifies the absence of arthritis activity and the right end (100) maximum arthritis activity.
Patient Acceptable Symptom State (PASS)
The patient's assessment of acceptable symptom state. Consist of one question answered with "yes" or "no". The question is: ''Take into account all the ways in which your arthritis has affected you in the past 48 hours. If you were to remain for the next few months as you are today, would it be acceptable to you?"
Anchoring question
The patient's assessment of change in arthritis activity since last visit from much worse to much better.
SLAQ flare score
Evaluates presence or severity of lupus flare on a transitional scale e.g. 0 (no worsening), 1 (mild worsening), 2 (moderate worsening) or 3 (severe worsening).
SLAQ symptom score
Evaluates the number of lupus specific symptoms present from 0-24. Higher score means worse outcome.
SLAQ total score
Evaluates severity of lupus disease activity by a weighted score of the 24 lupus specific symptoms, range 0-44. Higher score means worse outcome.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04411407
Brief Title
PROM Collected Via a WebApp Versus a Touch Screen Solution Among Patients With SLE
Official Title
Patient-reported Outcome Measures Collected in DANBIO Via a From Home Web Application Versus a Touchscreen in the Outpatient Clinic Among Patients With Systemic Lupus Erythematosus: A Randomised, Crossover, Agreement Study
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
July 15, 2020 (Actual)
Primary Completion Date
November 25, 2020 (Actual)
Study Completion Date
November 25, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Salome Kristensen
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
A randomised, within-participants cross-over design trial including 34 patients with systemic lupus erythematosus. The participants will be randomised to data registration of patient reported outcome measures (PROM) through the DANBIO webapp and thereafter via the outpatient touchscreen or vice versa.
Detailed Description
The aim of this trial is to evaluate whether electronic reporting of PROMs through the DANBIO web application (webapp) is comparable to the outpatient touchscreen among patients with SLE.
The trial is a randomised, crossover, agreement study where 34 patients with SLE from the Department of Rheumatology at Aalborg University Hospital will be included and randomised in ratio 1:1 to:
Group 1: PROMs are reported through the DANBIO webapp; thereafter, the touchscreen.
Group 2: PROMs are reported through the touchscreen; thereafter, the DANBIO webapp.
There will be a wash-out period of 1-2 day between the two registrations to minimise carryover bias.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Systemic Lupus Erythematosus
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
A randomised, within-participants, open, cross-over trial
Masking
None (Open Label)
Allocation
Randomized
Enrollment
34 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Group WT
Arm Type
Other
Arm Description
PROM registration via the DANBIO WebApp and thereafter the outpatient touchscreen
Arm Title
Group TW
Arm Type
Other
Arm Description
PROM registration via the outpatient touchscreen and thereafter the DANBIO WebApp
Intervention Type
Device
Intervention Name(s)
PROM registration via the DANBIO WebApp and the outpatient touchscreen in a randomised order
Intervention Description
PROM registration via the DANBIO WebApp and the outpatient touchscreen in a randomised order
Primary Outcome Measure Information:
Title
Change in Systemic Lupus Activity Questionnaire global health
Description
Evaluates global assessment of lupus activity using an NRS score from 0-10. Higher score Means worse outcome.
Time Frame
Day 1 (first data registration) and day 3 (second data registration)
Secondary Outcome Measure Information:
Title
Change in Health Assessment Questionnaire (HAQ)
Description
Assess the patient's physical function from 0-3. Higher score Means worse outcome.
Time Frame
Day 1 (first data registration) and day 3 (second data registration)
Title
Visual Analogue Scale for Pain
Description
The patient's assessment of pain on a scale from 0-100 within the last week.The left of the scale (0) signifies the absence of pain and the right end (100) maximum pain.
Time Frame
Day 1 (first data registration) and day 3 (second data registration)
Title
Visual Analogue Scale for fatigue
Description
The patient's assessment of fatigue on a scale from 0-100 within the last week. The left of the scale (0) signifies the absence of fatigue and the right end (100) maximum fatigue.
Time Frame
Day 1 (first data registration) and day 3 (second data registration)
Title
Patient Global Visual Analogue Scale
Description
The patient's global assessment of disease activity (arthritis severity) on a scale from 0-100 within the last week. The left of the scale (0) signifies the absence of arthritis activity and the right end (100) maximum arthritis activity.
Time Frame
Day 1 (first data registration) and day 3 (second data registration)
Title
Patient Acceptable Symptom State (PASS)
Description
The patient's assessment of acceptable symptom state. Consist of one question answered with "yes" or "no". The question is: ''Take into account all the ways in which your arthritis has affected you in the past 48 hours. If you were to remain for the next few months as you are today, would it be acceptable to you?"
Time Frame
Day 1 (first data registration) and day 3 (second data registration)
Title
Anchoring question
Description
The patient's assessment of change in arthritis activity since last visit from much worse to much better.
Time Frame
Day 1 (first data registration) and day 3 (second data registration)
Title
SLAQ flare score
Description
Evaluates presence or severity of lupus flare on a transitional scale e.g. 0 (no worsening), 1 (mild worsening), 2 (moderate worsening) or 3 (severe worsening).
Time Frame
Day 1 (first data registration) and day 3 (second data registration)
Title
SLAQ symptom score
Description
Evaluates the number of lupus specific symptoms present from 0-24. Higher score means worse outcome.
Time Frame
Day 1 (first data registration) and day 3 (second data registration)
Title
SLAQ total score
Description
Evaluates severity of lupus disease activity by a weighted score of the 24 lupus specific symptoms, range 0-44. Higher score means worse outcome.
Time Frame
Day 1 (first data registration) and day 3 (second data registration)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
110 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Diagnosed in DANBIO with SLE
Experience with the PROM questionnaires in DANBIO (≥ 1 previous assessments)
Exclusion Criteria:
Inability to provide informed consent or to comply with the study protocol
Diagnosis of SLE of ≥ 12 months
Does not have access to a device that can run the DANBIO webapp
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Salome Kristensen, MD, PhD
Organizational Affiliation
Department of Rheumatology, Aalborg University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Rheumatology
City
Aalborg
ZIP/Postal Code
9000
Country
Denmark
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
Study protocol and the SAP will be published as supplementary information to the article. IPD from this trial that underlie results in a publication will be made available in clinicaltrials.gov after publication of the article.
IPD Sharing Time Frame
Will be made available when the article is published
IPD Sharing Access Criteria
Study protocol and the SAP will be published as supplementary information to the article. IPD from this trial that underlie results in a publication will be made available in clinicaltrials.gov after publication of the article.
Learn more about this trial
PROM Collected Via a WebApp Versus a Touch Screen Solution Among Patients With SLE
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