Patient Reported Outcomes Reported Via PC / Tablet Home Versus Touch Screen at Hospital Among Patients With Arthritis

Not Applicable

Completed

• Conditions: Axial Spondyloarthritis; Rheumatoid Arthritis
• Interventions: Other: Reporting of patient reported outcome measures

• Registration Number: NCT02818478
• Lead Sponsor: Henrik Gudbergsen

Brief Summary

To investigate if electronic reporting of patient reported outcome measures from home is comparable to the traditional touch-screen solution to hospital among patients with rheumatoid arthritis and axial spondyloarthritis

Detailed Description

Not available

Study Timeline

• Study Start: 2016-05
• Study First Submitted: 2016-05-23
• Study First Submitted QC: 2016-06-28
• Study First Posted: 2016-06-29
• Primary Completion: 2016-12
• Study Completion: 2016-12
• Status Verified: 2017-02
• Last Update Submitted: 2017-02-07
• Last Update Posted: 2017-02-08

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 42

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
RA; outpatient clinic first	Reporting of patient reported outcome measures	Patients in this arm (10 patients with rheumatoid arthirtis, RA) will be randomised to initially fill in patient reported outcome measures at the outpatient clinic; subsequently these patients will fill in patient reported outcome measures from home via their own computer or tablet
AxSpa; outpatient clinic first	Reporting of patient reported outcome measures	Patients in this arm (10 patients with axial spondyloarthritis, AxSpa) will be randomised to initially fill in patient reported outcome measures at the outpatient clinic; subsequently these patients will fill in patient reported outcome measures from home via their own computer or tablet
RA; at home first	Reporting of patient reported outcome measures	Patients in this arm (10 patients with rheumatoid arthirtis, RA) will be randomised to initially fill in patient reported outcome measures from home via their own computer or tablet; subsequently these patients will fill in patient reported outcome measures at the outpatient clinic
AxSpa; at home first	Reporting of patient reported outcome measures	Patients in this arm (10 patients with axial spondyloarthritis, AxSpa) will be randomised to initially fill in patient reported outcome measures from home via their own computer or tablet; subsequently these patients will fill in patient reported outcome measures at the outpatient clinic

Primary Outcome Measures

Name	Time	Method
HAQ	48 hours	The Health Assessment Questionnaire (HAQ) developed to retrieve quantitative information on outcomes among patients with rheumatoid arthritis

Secondary Outcome Measures

Name	Time	Method
100 mm VAS global	48 hours	Assessed via a visual analogue scale (VAS)
100 mm VAS pain	48 hours	Assessed via a visual analogue scale (VAS)
100 mm VAS fatigue	48 hours	Assessed via a visual analogue scale (VAS)
BASDAI	48 hours	The Bath Ankylosing Spondylitis Disease Activity Index (BASDAI) developed to retrieve quantitative information on outcomes among patients with Ankylosing Spondylitis
BASFI	48 hours	The Bath Ankylosing Spondylitis Functional Index (BASFI) developed to retrieve quantitative information on outcomes among patients with Ankylosing Spondylitis
BASDAI 5 & 6	48 hours	Questions 5 and 6 in BASDAI