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Comparative effect of two supervised exercise programs on key health outcomes in women with fibromyalgia syndrome

Comparative effect of two supervised exercise programs on key health outcomes in women with fibromyalgia syndrome: a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN43742447
Enrollment
54
Registered
2009-12-21
Start date
2007-09-01
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

Fibromyalgia syndrome Musculoskeletal Diseases Other soft tissue disorders, not elsewhere classified

Interventions

Group A: Patients performed two aerobic exercise sessions per week, which included a 10 minute warm up, 25 - 30 minutes at 60 - 65% HRmax and interval training at 75 - 80% HRmax and finally 5 - 10 mi

Sponsors

University of Seville (Spain)
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Women aged above 18 years 2. Met the American College of Rheumatology (ACR) criteria for classification of fibromyalgia

Exclusion criteria

Exclusion criteria: 1. Presence of inflammatory rheumatic diseases 2. Severe psychiatric illness 3. Respiratory or cardiovascular diseases that prevent physical loading 4. Women with FM who attended another psychological or physical therapy

Design outcomes

Primary

MeasureTime frame
1. Health status: the Fibromyalgia Impact Questionnaire (FIQ) and The Medical Outcomes Study Short Form (SF-36) health survey 2. Physical fitness: the six-minute walk test was used to estimate aerobic capacity, hand-grip strength and range of motion (flexion/extension) in the shoulders and hips Assessment of all outcomes was undertaken at baseline and immediately after the 24-week intervention and at the same time points in the usual care control group.

Secondary

MeasureTime frame
Depression was assessed using the Beck Depression Inventory (BDI). Assessment of all outcomes was undertaken at baseline and immediately after the 24-week intervention and at the same time points in the usual care control group.

Countries

Spain

Outcome results

None listed

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