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Clinical Trials in Turkey / NCT07833280
Recruiting Observational

Kinesiophobia, Physical Activity, Sleep, and Quality of Life in Women With Chronic Pelvic Pain

NCT07833280 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2026-02-01
Last updated
2026-09-22

Condition(s) studied

Chronic Pelvic Pain Syndrome (CPPS)

Investigational drug(s) / intervention(s)

questionnaire

questionnaire: evaluation

Study summary

The study will include women who present to the Obstetrics and Gynecology outpatient clinic of Kırşehir Ahi Evran Training and Research Hospital with complaints of pelvic pain and are diagnosed with PCAS after a detailed examination, as well as healthy women. All included women will be administered the Tampa Kinesiophobia Scale (TKS), the International Physical Activity Questionnaire (Short), the Pittsburgh Sleep Quality Questionnaire (PSQI), and the Short Form 36 (p-36). The control group will consist of women who meet the inclusion and exclusion criteria but are not diagnosed with PCAS.

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
65 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. Being between 18-65 years of age 2. Having a diagnosis of Chronic Pelvic Pain 3. Having a pain score of 5 or higher on the visual analog scale 4. Voluntary participation in the study Exclusion Criteria: 1. Not wanting to continue in the study 2. Presence of neurological or orthopedic disease 3. Active urinary tract infection or recurrent urinary tract infection (more than 5 recurrent infections in the last 12 months) 4. Pregnancy 5. History of surgery in the pelvic region 6. Learning disability or other cognitive impairments.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Kırşehir Ahi Evran Üniversitesi Kırşehir Merkez Recruiting

More Ahi Evran University Education and Research Hospital trials in Turkey

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07833280 on ClinicalTrials.gov ↗ ← All trials in Turkey