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Effects of a Physical Exercise Program on Patients Affected With Fibromyalgia

Effects of a Physical Exercise Program on Patients Affected With Fibromyalgia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04031391
Enrollment
48
Registered
2019-07-24
Start date
2017-07-22
Completion date
2018-12-15
Last updated
2019-07-24

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

Conditions

Fibromyalgia

Keywords

physical activity, fibromyalgia, pain, exercice, quality of live

Brief summary

Physical activity has been used for a number of years in the treatment of fibromyalgia (FM). The main objective of this study is to compare the effects of physical activity on two groups of women diagnosed with fibromyalgia (FM) in terms of pain, quality of life and the impact of the condition on their daily lives. Methods: this was a randomized clinical trial to assess the effects of physical activity performed by subjects assigned to one of two groups on the scores of three questionnaires (the pain Visual Analogue Scale, the FIQ questionnaire and the SF-36 health questionnaire) administered before and after the intervention.

Interventions

OTHERPhysical activity

The intervention group: engaged in a therapeutic physical activity program involving low-intensity exercise, strength and balance work for 2 days a week over a 12-week period, with each session lasting 90 minutes. Both the intervention group and the control group separately completed the various baseline surveys which were part of the study. Once the intervention was over, they answered them again, also separately. The classes were led by an experienced physiotherapist who followed the physical exercise guidelines established by the American College of Sports Medicine (ACSM), although the intensity of the exercises was adapted to the participants' tolerance levels

Sponsors

Institut Catala de Salut
CollaboratorOTHER_GOV
Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

A randomized, multi-center, clinical trial composed of two groups response variables and a twelve weeks follow up.

Eligibility

Sex/Gender
FEMALE
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

Women * Ages of 40 and 75 * Diagnosis fibromyalgia (code M79.7) * Anoia region

Exclusion criteria

* Pregnant * Unable to participate in the physical activity program.

Design outcomes

Primary

MeasureTime frameDescription
The visual analogue scale (VAS)two monthsevaluate pain, with a score of 0 to 10
The Spanish version of the SF-36 questionnairetwo monthsused to assess their perceived state of health. It includes eight variables: vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role functioning and mental health
the Fibromyalgia Impact Questionnaire (FIQ)two monthsmeasures physical functioning, ability to undertake work and general well-being, with a score from 0 to 80.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026