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The Effectiveness of an Exercise regimen to Improve Sarcopenia, Sarcopenic Obesity, and Myokine Levels in Rheumatoid Arthritis

A Study to Estimate the Efficacy and Duration of Tailored Exercise to Improve Sarcopenia, Sarcopenic Obesity, and Myokine Levels in Rheumatoid Arthritis - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/100569
Enrollment
235
Registered
2026-01-08
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Health Condition 1: M059- Rheumatoid arthritis with rheumatoid factor, unspecified

Interventions

Intervention1: Tailored exercise regimen: Exercise regimen including a supervised strength training module, aerobic exercise and flexibility Control Intervention1: Nil: NOT APPLICABLE

Sponsors

Central Research and Publication Unit
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of diagnosed RA ACR-EULAR 2010 Criteria Sarcopenia as per AWGS criteria

Exclusion criteria

Exclusion criteria: 1.Diagnosed cases of end stage chronic kidney disease , decompensated chronic liver disease, Heart failure, infections, COPD, interstitial lung disease with functional impairment, permanent neurological disorders, cancers, or on medication for these 2. ACR functional status class IV : Limited ability to perform usual self-care, work, and hobbies. 3. Overlap with other connective tissue disease

Design outcomes

Primary

MeasureTime frame
To determine the efficacy of a tailored exercise regimen on the muscle mass, fat mass, sarcopenia and sarcopenic obesity as assessed by Bioelectrical impedance analysis (BIA) and clinical measures in sarcopenic patients of rheumatoid arthritisTimepoint: 4 weeks, 8 weeks, 12 weeks, 16 weeks and 24 weeks

Secondary

MeasureTime frame
To estimate levels of the myokine myostatin and exerkine irisin in this population pre and post intervention To determine the duration needed to achieve a change in the severity of sarcopenia To determine disease activity (DAS 28-CRP), fatigue (FACIT-F), disability (HAQ-DI), quality of life (EQ5D5L) pre and post the intervention To determine the associations between sarcopenia/sarcopenic obesity, disease parameters and myokine levels Timepoint: 4 weekly muscle mass assessment final time point-24 weeks

Countries

India

Contacts

Public ContactDr Varsha Bhatt

Bharati Vidyapeeth (Deemed to Be) University Medical College and Hospital ,Pune

varsha.rajat@bharatividyapeeth.edu8484056341

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026