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Connective Tissue Manipulation and Combined Ultrasound Therapy in Patients with Fibromyalgia

H

Hacettepe University

Status

Completed

Conditions

Fibromyalgia

Treatments

Procedure: connective tissue manipulation
Device: combined ultrasound therapy

Study type

Observational

Funder types

Other

Identifiers

NCT00302887
HEK06/12-39

Details and patient eligibility

About

The aim of this study was to evaluate the short term and one year follow-up results of connective tissue manipulation and combined ultrasound therapy (ultrasound and high voltage pulsed galvanic stimulation) in terms of pain, complaint of non-restorative sleep and impact on the functional activities in patients with fibromyalgia.

Full description

This is an observational prospective cohort study, investigating short and long term results of physiotherapy applications in 20 female patients with fibromyalgia. Physical characteristics of the subjects were recorded. Intensity of pain, complaint of non-restorative sleep, and impact of fibromyalgia on functional activities were evaluated by visual analogue scales. All evaluations were performed before and after 20 sessions of treatment, which included connective tissue manipulation of the back daily, for a total of 20 sessions and combined ultrasound therapy of the upper back region every other session. One year follow-up evaluations could be performed on 14 subjects.

Enrollment

20 patients

Sex

Female

Ages

19 to 68 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Women with pain depending to FM, with an intensity interfering to activities of daily living for a duration of at least six months, able to participate of 20 physiotherapy sessions within a four week period, volunteer for participating to the study without taking any drugs acting on the nervous system such as antidepressants, myorelaxants, analgesics or hypnotics, in the study period.

Exclusion criteria

evidence of neurological, infectious, endocrine and other inflammatory rheumatic diseases, and experience with any kind of manual and/or electrotherapy, within six months before the study.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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