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Novel Methods for Ascertainment of Gout Flares -A Pilot Study

Novel Methods for Ascertainment of Gout Flares -A Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02855437
Enrollment
44
Registered
2016-08-04
Start date
2016-09-30
Completion date
2018-08-31
Last updated
2019-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Gout

Brief summary

The purpose of this study is to determine the feasibility and acceptability of using different remote data collection technologies to ascertain flare occurrence among gout patients. Two technologies will be the focus of this study: a telephone based interactive voice response (IVR) and a smartphone mobile application (called RheumPRO). The results of this study will not only guide research approaches in clinical trials, but may also have direct implications for monitoring patient outcomes in the context of day-to-day clinical practice. The investigators hypothesize that acceptability will be greater for RheumPRO application than IVR. Additionally, the investigators hypothesize that RheumPRO will be associated with a greater frequency of patient-initiated interactions.

Detailed description

Acute gout flares are a major cause of morbidity. Flares lead to substantial reductions in health-related quality of life, increased work absenteeism, productivity loss, and substantial healthcare costs. Acute gout flares are likely related to more than 174,000 emergency department visits in the U.S. annually with corresponding charges approaching $166 million. In recent surveys, gout patients and healthcare providers alike identified the reduction of gout flares as the highest priority outcome that should be examined in future comparative effectiveness studies of urate lowering therapy (ULT) (unpublished results). Despite consensus about the importance of capturing flares, clinical trials investigating ULTs or anti-inflammatory prophylaxis have used inconsistent flare definitions and methods of flare ascertainment. The inconsistency has likely been driven by the absence of a standardized definition or ascertainment method. These deficits limit comparisons that can be made across investigations. Recently, a group supported by the American College of Rheumatology & European League Against Rheumatism (ACR & EULAR) has attempted to define a gout flare (8-10). For simplicity, the group focused on defining only those flares occurring after a definitive gout diagnosis. Nine elements of a flare definition emerged from the first two studies. These nine elements included physician reported information, laboratory data and patient self-report. In a third study, Gaffo et al. compared the discriminatory ability of the self-reported items against the gold standard of a rheumatologist's judgment of flare presence. Self-report of 4 criteria had the greatest discriminatory ability with an area under the curve (AUC) of 0.931. These promising results indicate the important role for a standardized self-report definition of a gout flare. In addition to variability in gout flare definitions, the optimal method for obtaining self-reported flares remains undefined. An early study of febuxostat, for example, assessed flares weekly at physician visits Another study counted a flare only when it was treated by a healthcare provider. Still other studies assessed flares during physician visits occurring at variable time points. These inconsistent methods also pose practical limitations given by their time and resource intensive nature. Opportunities to increase efficiency have only recently become available with the validation of the self-reported definition for gout flares described above. Self-report can now be combined with technological advances in remote data collection to develop novel and highly efficient methods to identify gout flares. The investigators propose a study to address this pressing need by leveraging technological advances that facilitate the remote and real-time collection of patient reported flares and outcomes (PROs) in gout.

Interventions

DEVICEIVR (Phone call)

IVR will auto dial participants at a schedule time. Participants complete questions using their phone keypad. Participants can also call the IVR to complete surveys if they experience a flare. The IVR will be programmed to call the patient weekly for 26 weeks to complete a weekly Gout Flare Survey and Patient Reported Outcomes Survey. Consistent with the published gout flare self-report definition, gout flare ascertainment questions will include whether the recent flare is similar to past flares, the number of swollen joints and the number of warm joints. Pain at rest during the attack will be assessed on a 0-9 scale. Further questions will include peak pain, timing of attack and duration of attack if completed. We will capture patient reported outcome measures (e.g. pain, fatigue, sleep) using instruments from NIH PROMIS. Following completion of 26 week IVR period participants will crossover to RheumPro arm.

DEVICERheumPro (Smartphone application)

RheumPRO will be programmed to notify participants weekly for 26 weeks via a scheduled pop-up to complete Gout Flare and Patient Reported Outcomes Surveys. Participants self-navigate through the survey questions using their smartphone. If participants do not complete the Gout Flare or Patient Reported Outcomes surveys RheumPro will generate 2 more pop-ups at the same time over the proceeding 2 days (eg. Tuesday 4 PM, Wednesday 4 PM). Participants can also open the RheumPro application on their smartphone and complete surveys or if they experience a flare on a day they are not scheduled to complete a survey. Following completion of 26 week RheumPro period participants will crossover to IVR arm.

Sponsors

University of Nebraska
CollaboratorOTHER
University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* \>/= to 18 yrs of age with Current physician diagnosed gout * current hyperuricemia (serum urate level \>6.8 mg/dl) * self-report of at least two gout flares in the previous 6 months * current smartphone user utilizing a FitBit compatible smart Phone (with the ability to download RheumPRO from Apple/Google Play store).

Design outcomes

Primary

MeasureTime frameDescription
Preference IVR vs RheumPRO6 monthsPercentage of total study population preferring IVR vs. RheumPRO
Feasibility of Using IVR vs. RheumPRO to Report Gout Flares6 monthsFeasibility ----Assessed by the percentage of participants completing answer IRV/RheumPRO queries.

Countries

United States

Participant flow

Recruitment details

The target population recruited was patients with gout. Patients were recruited from the UAB gout clinic, The Kirklin Clinic, and the UNMC gout clinic.

Participants by arm

ArmCount
Overall
Overall description of participants in the pilot study entitled, Novel Methods for Ascertainment of Gout Flares -A Pilot Study
44
Total44

Baseline characteristics

CharacteristicOverall
Age, Continuous49.3 years
STANDARD_DEVIATION 14.5
Age of first gout flare38.3 Years
STANDARD_DEVIATION 18.6
Number of flares prior 6 months
2-3 flares in prior 6 months
19 Participants
Number of flares prior 6 months
>=4 flares in prior 6 months
25 Participants
Race/Ethnicity, Customized
Race
Black or other race
14 Participants
Race/Ethnicity, Customized
Race
White race
30 Participants
Sex: Female, Male
Female
7 Participants
Sex: Female, Male
Male
37 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 00 / 0
other
Total, other adverse events
0 / 00 / 0
serious
Total, serious adverse events
0 / 00 / 0

Outcome results

Primary

Feasibility of Using IVR vs. RheumPRO to Report Gout Flares

Feasibility ----Assessed by the percentage of participants completing answer IRV/RheumPRO queries.

Time frame: 6 months

ArmMeasureValue (MEAN)Dispersion
Interactive Voice ResponseFeasibility of Using IVR vs. RheumPRO to Report Gout Flares81 percentage of weekly responseStandard Deviation 21
RheumPro Smartphone ApplicationFeasibility of Using IVR vs. RheumPRO to Report Gout Flares80 percentage of weekly responseStandard Deviation 25
Primary

Preference IVR vs RheumPRO

Percentage of total study population preferring IVR vs. RheumPRO

Time frame: 6 months

Population: Preference of IVR and StudyBuddy for reporting gout flares as reported by participants

ArmMeasureValue (COUNT_OF_PARTICIPANTS)
Interactive Voice ResponsePreference IVR vs RheumPRO3 Participants
RheumPro Smartphone ApplicationPreference IVR vs RheumPRO28 Participants

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026