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Sexual Dysfunction in Patients With Myofascial Pain Syndrome

K

Konya Beyhekim Training and Research Hospital

Status

Completed

Conditions

Sexual Dysfunction
Myofascial Pain Syndrome

Treatments

Other: visual pain scale (VASpain/fatigue), Beck depression index (BDI), the sexuality-importance score, sexual intercourse frequency

Study type

Observational

Funder types

Other

Identifiers

NCT05727566
KonyaBeyhekimTRH2022

Details and patient eligibility

About

This study evaluates the frequency of sexual dysfunction in women with myofascial pain syndrome and its relationship with clinical parameters.

Full description

The frequency of sexual dysfunction in reproductive-aged married women with primary myofascial pain syndrome will be evaluated in a prospective, cross-sectional survey-type study. The medical history of each participant was obtained and they underwent a detailed physical examination. Sociodemographic and clinic characteristics of all participants (age, education, marital status, employment status, family structure, income status, Body Mass Index(BMI), disease duration, number of pregnancies, sleep quality, etc.) were recorded. Pain and fatigue levels of the patients were measured by the visual pain scale (VAS), mood states by the Beck depression index (BDI), sexual function of the participants was assessed by the 0-10 Visual Analog Scale (VAS) to assess the degree of importance of sexuality (the sexuality-importance score). In addition, weekly/monthly sexual intercourse frequency was asked to all participants (patient and control groups). The questionnaires were administered to all participants in a room where they were alone with a female physician, and a suitable environment was provided for the patients to fill out the questionnaire. Patients were assured of the confidentiality of their information. Only questions that were not understood by the patient were explained without guidance.

Enrollment

90 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Myofascial pain syndrome (>3 months) was diagnosed in a female.
  • Being between the ages of 18 and 50, married, sexually active, and not menopausal
  • Volunteering to participate in the study, and being able to communicate easily.

Exclusion criteria

  • a history of systemic disease (cardiovascular, pulmonary, hepatic, renal, hematological, etc.)
  • major psychiatric illness, mental retardation
  • uncontrollable respiratory system problems
  • endocrine diseases, neurological diseases
  • previous hysterectomy or vaginal surgery, a history of sexually transmitted diseases
  • urinary or anal incontinence
  • limited motion in the upper or lower extremities
  • Fibromyalgia
  • inflammatory rheumatic diseases (such as rheumatoid arthritis, ankylosing spondylitis, etc.)
  • cervical/lumbar radiculopathy or myelopathy
  • communication problems
  • pregnancy, lactation
  • taking estrogen therapy
  • use antidepressant, anxiolytic, and antiepileptic drugs
  • chronic alcohol users

Trial design

90 participants in 2 patient groups

Patients with primer myofascial pain sydrome
Description:
pain for at least three months (myofascial pain) reproductive-aged married womens (18-50 years)
Treatment:
Other: visual pain scale (VASpain/fatigue), Beck depression index (BDI), the sexuality-importance score, sexual intercourse frequency
Healthy controls
Description:
Healthy control of reproductive-aged married women with compatible sociodemographic characteristics
Treatment:
Other: visual pain scale (VASpain/fatigue), Beck depression index (BDI), the sexuality-importance score, sexual intercourse frequency

Trial contacts and locations

1

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Central trial contact

Savas Karpuz; Ramazan Yilmaz, asist. prof

Data sourced from clinicaltrials.gov

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