Psoriatic Arthritis Clinical Trial
Official title:
EFFECT OF EXERCISE AND DIETARY WEIGHT LOSS ON SYMPTOMS AND SYSTEMIC INFLAMMATION IN OBESE ADULTS WITH PSORIATIC ARTHRITIS: RANDOMIZED CONTROLLED TRIAL
Psoriatic arthritis (PsA) is a particular pattern of inflammatory arthritis often seen in
association with psoriasis. PsA patients have a higher prevalence of comorbidities including
obesity, metabolic syndrome, depression and premature cardiovascular disease. There is
evidence that obesity is associated with PsA. A 12 month study was conducted to determine
whether exercise and dietary weight loss are more efficacious, either separately or in
combination, than standard care alone in improving symptoms and signs in obese adults with
PsA.
Fifty-five obese PsA patients with a body mass index (BMI) ≥30, were recruited. Patients
were randomized into usual lifestyle (controls), diet only, exercise only, and diet plus
exercise groups for 12 months. Disease activity was assessed. Blood samples collected after
12 hours overnight fasting were analysed for glucose, lipid profile, ESR, hsCRP,
proinflammatory cytokines; tumour necrosis factor alpha (TNF-alpha), interleukin-6 (IL-6)
and interleukin-17 (IL-17). The primary outcome measures included improvement in ACR20.
Secondary endpoints included reduction in PASI score, DAS28-CRP response and physician and
patient global assessment (PGA). Safety and tolerability were also assessed. Data was
collected at baseline and every 6 months.
There is evidence that obesity is associated with PsA. Obesity leads to increased
proinflammatory cytokines which may contribute to the development of multiple disturbances
in PsA patients.
A 12 month, randomized single blind clinical trial was conducted to determine whether
long-term exercise and dietary weight loss are more efficacious, either separately or in
combination, than standard care alone in improving physical function, pain, fatigue,
depression and systemic inflammation in obese adults with PsA.
Fifty-five obese ethnically homogenous adult PsA patients with a body mass index (BMI) ≥30,
who satisfied the classification of psoriatic arthritis criteria were recruited. Patients
were randomized into usual lifestyle (controls), diet only, exercise only, and diet plus
exercise groups together with the continued use of standard treatment.
Exclusion criteria included other inflammatory conditions. Detailed skin and rheumatological
assessment was conducted. Disease activity was assessed by psoriasis area and severity index
(PASI), disease activity score (DAS28CRP), Health Assessment Questionnaire- Disability Index
(HAQ-DI), Beck's Depression Inventory (BDI) and fatigue numeric rating scale. Blood samples
collected after 12 hours overnight fasting were analysed for glucose, lipid profile, ESR,
hsCRP, proinflammatory cytokines; tumour necrosis factor alpha (TNF-alpha), interleukin-6
(IL-6) and interleukin-17 (IL-17). The primary outcome measures included improvement in
ACR20, systemic inflammation markers, BMI, physical function, pain, fatigue, depression and
HAQ-DI. Secondary endpoints included reduction in PASI score, DAS28-CRP response and
physician and patient global assessment (PGA). Safety and tolerability were also assessed.
Data was collected at baseline and every 6 months.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT04152759 -
Comparative Study to Evaluate the Pharmacokinetics of BAT2506 vs Simponi® in Healthy Subjects
|
Phase 1 | |
Completed |
NCT03248518 -
Lessening the Impact of Fatigue in Inflammatory Rheumatic Diseases
|
N/A | |
Completed |
NCT01925768 -
Safety and Efficacy Study of Apremilast to Treat Psoriatic Arthritis
|
Phase 3 | |
Completed |
NCT01892436 -
Extension Study up to 3 Years for Secukinumab in Psoriatic Arthritis
|
Phase 3 | |
Completed |
NCT01212770 -
PALACE 3: Efficacy and Safety Study of Apremilast to Treat Active Psoriatic Arthritis
|
Phase 3 | |
Completed |
NCT05051943 -
A Study of the Real-world Use of an Adalimumab Biosimilar and Evaluation of Nutritional Status on the Therapeutic Response
|
||
Completed |
NCT01212757 -
PALACE 2: Efficacy and Safety Study of Apremilast to Treat Active Psoriatic Arthritis
|
Phase 3 | |
Completed |
NCT03953378 -
CD73+ Th1.17 in Rheumatoid Arthritis and Psoriatic Arthritis
|
||
Recruiting |
NCT02572700 -
Pain Mechanisms and Ultrasonographic Disease Activity in Psoriatic Arthritis
|
||
Completed |
NCT02556034 -
Assessment of Tender & Swollen Joints Count Score Performed by a Rheumatologist And Rheumatology Nurses in Patients With RA and PsA.
|
||
Completed |
NCT02154425 -
A Multicenter, Postmarketing Study Evaluating the Concentration of Cimzia® in Mature Breast Milk of Lactating Mothers
|
Phase 1 | |
Completed |
NCT02188654 -
Metformin in Psoriatic Arthritis
|
N/A | |
Completed |
NCT02164214 -
Does Etanercept Influence Tweak Modulation of Inflammation During Inflammatory Rheumatisms (Psoriatic Arthritis and Rheumatoid Arthritis)?
|
Phase 3 | |
Completed |
NCT01392326 -
Efficacy at 24 Weeks and Long Term Safety, Tolerability and Efficacy up to 2 Years of Secukinumab (AIN457) in Patients With Active Psoriatic Arthritis (PsA)
|
Phase 3 | |
Completed |
NCT01083693 -
Quality of Life Outcomes of HUMIRA in Rheumatoid Arthritis (RA), Psoriatic Arthritis (PsA), Ankylosing Spondylitis (AS) After Unsustainable Response to Biologicals and Disease Modifying Antirheumatic Drugs
|
N/A | |
Not yet recruiting |
NCT00517101 -
Presence of IBD Specific Antibodies (ASCA, ALCA, ACCA, AMCA) in the Sera of Patients With Spondyloarthropathy
|
N/A | |
Completed |
NCT00133315 -
TNFalfa Blocking Treatment of Spondylarthropathies
|
Phase 4 | |
Completed |
NCT00659412 -
A Placebo-controlled Study With an Extension Examining the Safety and Efficacy of Alefacept in Psoriatic Arthritis
|
Phase 2 | |
Completed |
NCT00946686 -
To Demonstrate the Relative Bioavailability, Parallel Study Of Leflunomide 20 mg Tablets Under Fasting Conditions
|
Phase 1 | |
Not yet recruiting |
NCT06059430 -
Cohort Project of Patients With Inflammatory Rheumatism
|