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Effects of Two Different Applications in Fibromyalgia

Not Applicable
Completed
Conditions
Fibromyalgia
Interventions
Other: Connective tissue massage
Other: Kinesio Tape Application
Registration Number
NCT05897931
Lead Sponsor
Biruni University
Brief Summary

The study aims to determine the effect of connective tissue massage and taping applications on the pain and depression complaints of fibromyalgia patients and to compare their impact on quality of life.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
34
Inclusion Criteria
  • Being diagnosed with fibromyalgia.
  • Be in the age range of 20 - 55 years.
  • To be a volunteer participant in the research.
  • Being able to communicate comfortably.
  • To be able to act independently.
Exclusion Criteria
  • Having had a surgical operation within the last year.
  • Presence of significant infection.
  • Being diagnosed with cancer.
  • Being pregnant or breastfeeding.
  • Being addicted to drugs or alcohol.
  • Having a cognitive problem.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Connective tissue massageConnective tissue massageParticipants will receive TENS and infrared treatment for 25 minutes, 5 days a week. Then Connective Tissue Massage will be applied.
Kinesio Tape ApplicationKinesio Tape ApplicationParticipants will receive TENS and infrared treatment for 25 minutes, 5 days a week. Kinesio tape application will be applied 2 days a week for 4 weeks.
Primary Outcome Measures
NameTimeMethod
Visual Analogue Scale4 weeks

Visual Analogue Scale (VAS) will be used to assess pain severity. In the assessment, the patient is asked to mark pain intensity on a 10-centimeter line that no pain is 0, and the most severe pain is 10.

Secondary Outcome Measures
NameTimeMethod
Fibromyalgia Impact Questionnaire4 weeks

The questionnaire assesses the functional status of patients with fibromyalgia. The scale consists of 20 questions that measure physical function, well-being, difficulty in doing work, not being able to go to work, fatigue, stiffness, morning fatigue, pain, anxiety, and depression separately. Low scores indicate improvement or less effect in patients.

McGill Pain Questionnaire4 weeks

The quality of the pain felt by the patients will be evaluated with the Short Form McGill Pain Questionnaire. The level of severity felt by the patient is evaluated with a number scale (0=no, 1=mild, 2=moderate, 3=severe), and higher scores show severe pain intensity.

Beck's Depression Inventory4 weeks

The Beck's Depression Inventory (BDI) is a 21-item self-assessment scale that evaluates the patients' perceived depressive symptoms quantitatively and measures the symptoms of depression. The higher scores indicate the severity of the patient's depression. It has been suggested that those who score 17 and above on the BDI may constitute an at-risk group.

Short Form-36 Quality of Life Scale4 weeks

The scale assesses the quality of life. The scale consists of 36 items evaluated in 8 separate subscales. The score from each subscale is between 0-100, and a higher score indicates better quality of life.

Trial Locations

Locations (1)

Yeditepe University

🇹🇷

Istanbul, Turkey

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