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Kinesio Taping and Inhibitory Treatment Techniques

Benefits of Kinesio Taping and Inhibitory Treatment Techniques in Patients With Fibromyalgia Syndrome

Status
Suspended
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02859467
Enrollment
64
Registered
2016-08-09
Start date
2016-08-31
Completion date
2024-06-30
Last updated
2023-09-21

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

Conditions

Fibromyalgia

Keywords

Physical Therapy Modalities, Exercise, Electrical Stimulation Therapy, Bandages

Brief summary

Objective: Compare the benefits of Kinesio Taping and Inhibitory Treatment Techniques for Cervical, Thoracic and Lumbar Spine in Patients with Fibromyalgia Syndrome (FMS). Study Design: A single-blind randomized controlled trial was conducted on patients with FMS. Setting: Clinical setting. Methods: Sixty-four subjects with FMS were randomly assigned to an experimental group receiving kinesio taping and inhibitory treatment techniques, or to a control group for exercises and electrical stimulation therapy.

Interventions

OTHERKinesio Taping and Inhibitory Treatment Techniques

Kinesio Taping on trapezius, infraspinatus, and paravertebral muscles Inhibitory Treatment Techniques: * Release Technique of the trapezius muscle. * Release Technique for scalene muscles. * Technique suboccipital inhibition. * Technique hands crossed for induction dorsal superficial fascia.

OTHERExercise and Electrical Stimulation Therapy

Session for general physical activities (joint mobility, muscle strength and elasticity), and electrical stimulation therapy on para vertebral muscles.

Sponsors

Universidad de Almeria
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosed Fibromyalgia Syndrome. * Limitation of usual activities due to pain on at least 1 day in the previous 30 days. * Agreement to attend evening therapy sessions. * Non-practice of regular physical activity.

Exclusion criteria

* A history of surgery. * The presence of comorbid conditions (e.g., morbid obesity, inflammatory diseases, irritable bowel syndrome and interstitial cystitis). * A history of whiplash injury. * Severe physical disability. * uncontrolled endocrine disorders (e.g., hyperthyroidism, diabetes); 6) illness (e.g., schizophrenia or substance abuse). * The use of medication other than as-needed analgesics (excluding long-term narcotics). * Malignancy. * Psychiatric disorders. * A score of ≥ 9 points in the Beck depression inventory.

Design outcomes

Primary

MeasureTime frameDescription
Pain IntensityChanges from Baseline, and 10 weeksA 10-point Numerical Pain Scale (0: no pain, 10: maximum pain) assesses the intensity of pain.

Secondary

MeasureTime frame
Pittsburgh Quality of Sleep QuestionnaireChanges from Baseline, and 10 weeks
Beck Inventory for DepressionChanges from Baseline, and 10 weeks
Fibromyalgia Impact Questionnaire (FIQ)Changes from Baseline, and 10 weeks
Hospital Anxiety Depression Scale (HADS)Changes from Baseline, and 10 weeks
State-Trait Anxiety Inventory (STAI)Changes from Baseline, and 10 weeks
McGill Pain QuestionnaireChanges from Baseline, and 10 weeks
Quality of Life (SF-36)Changes from Baseline, and 10 weeks
Pain PressureChanges from Baseline, and 10 weeks
Schöber TestChanges from Baseline, and 10 weeks
Widespread pain indexChanges from Baseline, and 10 weeks
Symptom severity scoreChanges from Baseline, and 10 weeks
Measurement Finger-Floorsymptom severity scale
Fatigue Impact ScaleChanges from Baseline, and 10 weeks

Countries

Spain

Outcome results

None listed

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