search
Back to results

Acute Response to Exercise in Patients With Rheumatoid Arthritis

Primary Purpose

Rheumatoid Arthritis

Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Exercise
Sponsored by
University of Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rheumatoid Arthritis

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Adult women diagnosed with rheumatoid arthritis under pharmacological treatment, for at least 6 months, with a monoclonal antibody against the interleukin-6 receptor or TNF-alpha inhibitors;
  • Stable dose of monoclonal antibody against the interleukin-6 receptor or TNF-alpha inhibitors in the previous 3 months;

Exclusion Criteria:

  • Any physical limitation or disability that preclude exercise participation;
  • Participation in a structured exercise program in the previous 12 months;

Sites / Locations

  • Univsersity of Sao PauloRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

IL-6 blockade

Anti-TNF-alpha

Healthy controls

Arm Description

RA patients under pharmacological treatment with interleukin-6 blockade.

RA patients under pharmacological treatment with anti-TNF-alpha.

Healthy participants.

Outcomes

Primary Outcome Measures

Insulin sensitivity
Acute effect of exercise on insulin sensitivity assessed by the hyperinsulinemic euglycemic clamp.

Secondary Outcome Measures

Insulin sensitivity-related molecular pathway (Western Blotting)
Insulin sensitivity-related molecular pathway will be assessed by Western Blotting.
Insulin sensitivity-related molecular pathway (RT-PCR)
Insulin sensitivity-related molecular pathway will be assessed by Real-Time Polymerase Chain Reaction (RT-PCR).
Skeletal muscle glucose uptake
Positron emission tomography-magnetic resonance imaging (PET/MRI) will be performed to quantify skeletal muscle glucose uptake.

Full Information

First Posted
June 3, 2021
Last Updated
August 23, 2021
Sponsor
University of Sao Paulo
search

1. Study Identification

Unique Protocol Identification Number
NCT04927546
Brief Title
Acute Response to Exercise in Patients With Rheumatoid Arthritis
Official Title
Impact of Interleukin-6 Receptor Blockade on Acute Response to Exercise on Insulin Sensitivity and Muscle Glucose Uptake in Patients With Rheumatoid Arthritis
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
August 2021 (Anticipated)
Primary Completion Date
July 2023 (Anticipated)
Study Completion Date
July 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo

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
Rheumatoid arthritis (RA) is a chronic inflammatory disease that affects the joints, causing pain, edema, physical disability and poor quality of life. In addition, RA patients are at increased risk of developing cardiovascular disease (CVD) and premature death. The most effective pharmacological treatment is the use of biological agents that inhibit the action of specific substances, such as interleukin 6 (IL-6) and tumor necrosis factors (TNF). Physical exercise is considered a first-line non-pharmacological treatment in RA, improving inflammatory and metabolic profile, functional capacity, fatigue and preventing the onset of CVD. There is evidence that IL-6, when secreted as a result of exercise, brings several benefits. However, there is no study investigating the interaction between biological IL-6 blocking agents and exercise on metabolic responses, such as insulin sensitivity and glucose uptake, in patients with RA. To answer this question, adult women diagnosed with RA and healthy controls will be recruited for an acute session of exercise. RA patients will be divided into 2 groups, according to the pharmacological treatment (tocilizumab or anti-TNF). The acute responses of insulin sensitivity after an acute session of exercise will be assessed by the hyperinsulinemic euglycemic clamp, and the molecular pathways will be assessed by muscle biopsy and gene and protein expression analysis. Positron emission tomography-magnetic resonance imaging (PET/MRI) will be performed to quantify skeletal muscle glucose uptake.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rheumatoid Arthritis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
RA patients will be divided into 2 groups, according to the pharmacological treatment (tocilizumab or anti-TNF). A third group will be composed by healthy controls. The acute responses of insulin sensitivity after an acute session of exercise will be assessed by the hyperinsulinemic euglycemic clamp, and the molecular pathways will be assessed by muscle biopsy and gene and protein expression analysis. Positron emission tomography-magnetic resonance imaging (PET/MRI) will be performed to quantify skeletal muscle glucose uptake.
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
IL-6 blockade
Arm Type
Experimental
Arm Description
RA patients under pharmacological treatment with interleukin-6 blockade.
Arm Title
Anti-TNF-alpha
Arm Type
Experimental
Arm Description
RA patients under pharmacological treatment with anti-TNF-alpha.
Arm Title
Healthy controls
Arm Type
Experimental
Arm Description
Healthy participants.
Intervention Type
Behavioral
Intervention Name(s)
Exercise
Intervention Description
Thirty minutes of aerobic exercise in a treadmill.
Primary Outcome Measure Information:
Title
Insulin sensitivity
Description
Acute effect of exercise on insulin sensitivity assessed by the hyperinsulinemic euglycemic clamp.
Time Frame
1 hour post-exercise
Secondary Outcome Measure Information:
Title
Insulin sensitivity-related molecular pathway (Western Blotting)
Description
Insulin sensitivity-related molecular pathway will be assessed by Western Blotting.
Time Frame
Baseline and 4 hours post-exercise
Title
Insulin sensitivity-related molecular pathway (RT-PCR)
Description
Insulin sensitivity-related molecular pathway will be assessed by Real-Time Polymerase Chain Reaction (RT-PCR).
Time Frame
Baseline and 4 hours post-exercise
Title
Skeletal muscle glucose uptake
Description
Positron emission tomography-magnetic resonance imaging (PET/MRI) will be performed to quantify skeletal muscle glucose uptake.
Time Frame
3 hours post-exercise

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Adult women diagnosed with rheumatoid arthritis under pharmacological treatment, for at least 6 months, with a monoclonal antibody against the interleukin-6 receptor or TNF-alpha inhibitors; Stable dose of monoclonal antibody against the interleukin-6 receptor or TNF-alpha inhibitors in the previous 3 months; Exclusion Criteria: Any physical limitation or disability that preclude exercise participation; Participation in a structured exercise program in the previous 12 months;
Facility Information:
Facility Name
Univsersity of Sao Paulo
City
Sao Paulo
ZIP/Postal Code
05508-030
Country
Brazil
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bruno Gualano, Phd
Phone
551126618022
Email
gualano@usp.br
First Name & Middle Initial & Last Name & Degree
Bruno Gualano, Phd

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Acute Response to Exercise in Patients With Rheumatoid Arthritis

We'll reach out to this number within 24 hrs