Predictive Utility of a Short-term Improvement in Objectively Measured Physical Activity in Rheumatoid Arthritis (PUSIPA)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorEsbjerg Hospital - University Hospital of Southern Denmark

About this trial

SUMMARY Background: Several studies have shown physical activity (PA) to be inversely correlated to disease activity in rheumatoid arthritis (RA) patients. However, it is unclear whether improved PA leads to lower disease activity or if low disease activity predicts improved PA in rheumatoid arthritis patients. Furthermore, it is unknown how fibromyalgia (FM) affects this interaction.

Objective(s): Our primary objective will be to compare the effect of an immediate improvement in physical activity after one week on the proportion of RA patients achieving low disease activity after 12 weeks of biological treatment. Furthermore, we will explore whether the presence of concomitant FM affects this clinical response (i.e., interaction between FM status and PA response).

Design: A prospective cohort study in the form of a target-trial attempting to address a causal question comparing the outcome among the participants with an immediate improvement in physical activity, relative to individuals without.

Setting and patients: Biologically naive RA patients initiating biological treatment are consecutively enrolled. PA is quantified by accelerometry one week prior to, one week after, and after 3 months of biological treatment.

Sample size: 100 RA patients starting biological therapy is planned enrolled in the study.

Measurements: RA patients will be divided into two groups depending on their improvement in physical activity after onset of biological treatment. The percentage of time spent in moderate-to-vigorously physical activity (MVPA) i.e., the percentage of time a patient is in motion \[walking, running, bicycling, or swimming\] is measured prior to, one week, and approximately 3 months after biological treatment onset, respectively. The MVPA ratio (MVPA After biological treatment/MVPA Before biological treatment) will divide patients enabling a contrast between two groups: Those with high improvement considering MVPA (after 1 week; the upper tertile of MVPA ratio of the sample) and those without. Treatment response (achieving a disease activity score \< 3.2) after approximately 3 months from baseline will be analyzed as the contrast between groups.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with RA (> 18 years of age)

Patients who are to be treated with a biological agent

Patients who can read and understand Danish

Disqualifiers

Patients who are physically impaired (patients depending on assistance devices for walking)

Pregnancy

Patients who have received corticosteroids two weeks prior to and during the period of the movement measurement

Patients who by virtue of illiteracy or cognitive impairment, are unable to complete the questionnaire.

Trial population

Patients with RA (\> 18 years of age) who are to be treated with a biological agent.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

MVPA ratio before and after biological therapy

Time spent in moderate-to-vigorously physical activity before and after biological therapy. Continous meassure will be performed during 1 week.

Time frame
at baseline, after 1 week and after 12 weeks from treatment initiation.
2

Disease activity score (DAS)

DAS score will be uptained at each visit (0-10, where 10 represent maximum disease activity)

Time frame
at baseline, after 1 week and after 12 weeks from treatment initiation.

Secondary outcomes

1

Fibromyalgia

Fibromyalgia score according to the 2016 criteria for fibromyalgia (0-31, where 31 represents worst outcome)

Time frame
at baseline, after 1 week and after 12 weeks from treatment initiation.
2

Fatigue

Fatigue score according to the Bristol Rheumatoid arthritis fatigue scale (0-70 where 70 represent maximum level of fatigue)

Time frame
at baseline, after 1 week and after 12 weeks from treatment initiation.

Other outcomes

1

Physical activity scores on questionnaire

Questionnaires will be emplyed to evaluate level of physical activity meassured by questionnaire compared to the accelerometry motion device. This will be performed descriptly

Time frame
at baseline, after 1 week and after 12 weeks from treatment initiation.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.