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Impact of exercise on body fat and symptoms in Rheumatoid Arthritis patients

A Longitudinal Study on Adipose Tissue Distribution, Its Changes Following a Structured Exercise Program and Its Correlation with Disease Activity in Rheumatoid Arthritis. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/02/104076
Enrollment
102
Registered
2026-02-17
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

Health Condition 1: D50-D89- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

Interventions

Intervention1: Structured, Supervised Exercise Program: Aerobic Training: Outdoor walking or stationary cycling for 30 minutes per session, 3 times per week. Resistance Training: Exercises focused on

Sponsors

Medanta - The Medicity, Gurugram
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Age between eighteen and fifty years, either gender Diagnosed with rheumatoid arthritis according to the two thousand ten ACR EULAR classification criteria Disease duration between six months and five years Active disease with DAS twenty eight ESR greater than three point one On stable standard medical treatment for rheumatoid arthritis Willing to undergo dual energy X ray absorptiometry assessment Willing to participate in a six month structured aerobic and resistance exercise program Able to comply with study procedures and follow up assessments Written

Exclusion criteria

Exclusion criteria: Presence of any other autoimmune or systemic inflammatory disorder Uncontrolled medical conditions such as cardiovascular disease diabetes hypertension dyslipidemia or hypothyroidism Current or past history of malignancy Pregnant or lactating women Contraindication to dual energy X ray absorptiometry assessment Body mass index more than thirty five Any musculoskeletal neurological or cardiopulmonary condition limiting safe participation in exercise Inability or unwillingness to comply with study protocol

Design outcomes

Primary

MeasureTime frame
Visceral adipose tissue Subcutaneous adipose tissue Rheumatoid arthritis disease activity measured by DAS twenty eight ESRTimepoint: at baseline, 4 weeks & 8 weeks

Secondary

MeasureTime frame
Handgrip strength Functional disability assessed by health assessment questionnaire disability index Systemic inflammatory markers erythrocyte sedimentation rate & C reactive protein Body composition parameters measured by dual energy X ray absorptiometry Correlation between adipose tissue distribution & disease activityTimepoint: at baseline, 4 weeks & 8 weeks

Countries

India

Contacts

Public ContactKanika Markan

Noida International University

sranjana@rediffmail.com9654873085

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Mar 14, 2026