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High Intensity Training in patients with rheumatoid arthritis

High Intensity Training in rheumatoid arthritis (RA)-molecular pathways related to inflammation, fatigue and pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN62313758
Enrollment
20
Registered
2008-07-24
Start date
2008-08-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Rheumatoid arthritis (RA) Musculoskeletal Diseases Seropositive rheumatoid arthritis

Interventions

The intervention group will participate in strength training three times a week in a 75-minute training program for 12 weeks. Eight major muscle groups will each be trained in three sets of eight repe

Sponsors

ALF Foundation (Sweden)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Twenty female patients after menopause 2. RA according to American College of Rheumatology criteria 3. Less than 12 months since diagnosis 4. Stable medication since at least three months 5. Independent in daily living 6. Passed menopause 7. Speak and understand Swedish 8. No other major disease that prevent them from performing intensive strength training

Exclusion criteria

Exclusion criteria: Does not comply with the above inclusion criteria.

Design outcomes

Primary

MeasureTime frame
Static and isokinetic muscle strength in knee extensors and knee flexors measured electronically with the Kin-Com. Both the primary and the secondary outcomes will be measured at baseline and at three month follow up.

Secondary

MeasureTime frame
1. Clinical outcome (body functions, pain, fatigue and perceived health) 2. Inflammation 3. Pain mechanisms 4. Comorbidity 5. Muscle biopsies from vastus lateralis analysed for reactive oxygen species/reactive nitrogen species and expression of oestrogen receptors in muscles from patients with RA patients and controls before and after the intervention Both the primary and the secondary outcomes will be measured at baseline and at three month follow up.

Countries

Sweden

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026