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Comparative Study About the Effect of Aquatic Therapy vs Land-based Therapy in Women With Fibromyalgia

Comparative Study About the Effect of a Physical Therapy Protocol in Warm Water vs Land-based Therapy in Women With Fibromyalgia Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02695875
Enrollment
40
Registered
2016-03-01
Start date
2016-02-29
Completion date
2024-12-31
Last updated
2025-04-02

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

Conditions

Fibromyalgia

Keywords

Fibromyalgia, Pain, Postural balance, Physical therapy, Aquatic therapy

Brief summary

Fibromyalgia is a disease whose incidence rate is increasing and causing a severe disability to those who suffer it. Currently, other treatment resources are being implemented, such as aquatic therapy. This therapy seems to provide positive results in different dimensions of fibromyalgia. The main objective of the study is to determine the effectiveness of a physical therapy program in warm water vs. land-based therapy in women with fibromyalgia for pain reduction and improvement balance at the end of treatment and a month and a half later (follow-up). The type of study is a randomized controlled opened trial. The sample is composed of 34 women with age between 35 and 64 years and fibromyalgia diagnosis who will be divided into 2 groups: Aquatic Therapy Group (n=17) and Land-Based Therapy Group (n=17). This study will have two primary outcomes: Pain and balance. The intensity of pain will be assessed using the visual analog scale (VAS) and the pain threshold for each one of the 18 tender points will be assessed using a electronic algometer. Static balance will be evaluated with the Romberg's test and the dynamic balance with the Timed Up & Go test (TUG) and Berg Balance Scale. Both type of balance will be recorded in slow motion and then, will be analysed with a motion software. Secondary outcomes are: The impact of fibromyalgia on patient's lives, that will be measured with the Revised Fibromyalgia Impact Questionnaire (FIQR); the sleep quality, that will be assessed with the Pittsburgh Sleep Quality Index (PSQI); the fatigue, that will be evaluated witn the Multidimensional Fatigue Inventory (MFI); the physical capacity, that will be measured with the six minute walk test (SMWT) and confidence in balance that will be assessed with the Activities-specific Balance Confidence scale (ABC). Each intervention will last one hour and will be made 3 times a week for three months . It will consist of 4 sections: Warming, exercises for static and dynamic balance training, stretching and relaxation. Statistical analysis will be made using the Statistical Package for the Social Sciences software, version 21.0 for Windows. p ≤ 0.05 will be the significance level set for all analysis.

Interventions

The material is contributed by Faculty of Physiotherapy at University of A Coruña. The exercises that will be made during treatment, are designed and developed to improve core muscles and, in this way, improve postural balance.

Pool material is contributed by Maria José Jove Foundation. The exercises that will be made during treatment, are designed and developed to improve core muscles and, in this way, improve postural balance.

Sponsors

Universidade da Coruña
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
35 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Female. * Age range between 35 and 64 years. * Diagnosis of fibromyalgia according to the criteria of the American College of Rheumatology (ACR) in 1990 and 2010. * Mark ≥ 4 on the Visual Analogue Scale (VAS). * Mark ≥ 5 on the Visual Analogue Scale for balance included in The Revised Fibromyalgia Impact Questionnaire (FIQR).

Exclusion criteria

* History of severe trauma. * Neurological diseases (stroke, Parkinson's disease, dementia). * Frequent migraines. * Inflammatory rheumatic diseases. * People who have been treated in the past six months by traumatic injuries. * Being pregnant. * Visual or hearing deficits uncorrected. * Infectious diseases. * Severe cardiovascular disease. * People who do exercise regularly more than 20 minutes, more than 3 times a week in the past 3 months.

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline Pain at 3 months of therapy and one month and a half after treatment.It will be measured at baseline, at 3 months of therapy and one month and a half after treatment (follow-up).Pain will be assessed using the visual analog scale (VAS).
Change from baseline Static Balance at 3 months of therapy and one month and a half after treatment.It will be measured at baseline, at 3 months of therapy and one month and a half after treatment (follow-up).It will be evaluated with the Romberg's test, whose execution will be filmed in slow motion and then, these videos will be analysed with a motion software.
Change from baseline Dynamic Balance at 3 months of therapy and one month and a half after treatment.It will be measured at baseline, at 3 months of therapy and one month and a half after treatment (follow-up).It will be assessed using the Timed Up & Go test (TUG), whose execution will be filmed in slow motion and then, these videos will be analysed with a motion software.

Secondary

MeasureTime frameDescription
Change from baseline Sleep Quality at 3 months of therapy and one month and a half after treatment.It will be measured at baseline, at 3 months of therapy and one month and a half after treatment (follow-up).It will be assessed with the Pittsburgh Sleep Quality Index (PSQI).
Change from baseline Fatigue at 3 months of therapy and one month and a half after treatment.It will be measured at baseline, at 3 months of therapy and one month and a half after treatment (follow-up).It will be evaluated with the Multidimensional Fatigue Inventory (MFI).
Change from baseline Confidence in Balance at 3 months of therapy and one month and a half after treatment.It will be measured at baseline, at 3 months of therapy and one month and a half after treatment (follow-up).It will be assessed with the Activities-specific Balance Confidence scale (ABC).
Change from baseline Functional Independence to perform activities of daily living at 3 months of therapy and one month and a half after treatment.It will be measured at baseline, at 3 months of therapy and one month and a half after treatment (follow-up).It will be assessed using the Berg Balance Scale.
Change from baseline Physical Capacity at 3 months of therapy and one month and a half after treatment.It will be measured at baseline, at 3 months of therapy and one month and a half after treatment (follow-up).It will be measured with the six minute walk test (SMWT).
Change from baseline Pain Threshold for each one of the 18 tender points established at 3 months of therapy and one month and a half after treatment.It will be measured at baseline, at 3 months of therapy and one month and a half after treatment (follow-up).It will be assessed using an electronic algometer.
Change from baseline Quality of Life at 3 months of therapy and one month and a half after treatment.It will be measured at baseline, at 3 months of therapy and one month and a half after treatment (follow-up).It will be measured with the Revised Fibromyalgia Impact Questionnaire (FIQR).

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026