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Not yet recruiting NCT07487025

Knowledge, Coping Strategies, and Sexual Function in Chronic Pelvic Pain

Observational Chronic Pelvic Pain Chronic Pain

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Chronic Pelvic Pain, Chronic Pain. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Association Between Knowledge About Pain, Coping Strategies, and Sexual Function in Adults With Chronic Pelvic Pain: A Cross-Sectional Observational Study

Overview

This study aims to explore the relationships between knowledge about pain, coping strategies, and sexual function in adults with chronic pelvic pain. Chronic pelvic pain is a persistent condition that can affect physical health, emotional wellbeing, and daily life. Research suggests that understanding of pain and coping responses may influence how people experience chronic pain and its impact on quality of life. Participants will be adults diagnosed with chronic pelvic pain who attend hospital outpatient clinics. Those who agree to participate will complete a set of questionnaires assessing knowledge about pain, coping strategies, sexual function, and basic demographic and pain-related information. Participation is voluntary and anonymous and involves a single assessment session lasting approximately 10-15 minutes. No treatments or interventions are provided as part of this study. The results will contribute to understanding how knowledge about pain, coping strategies, and sexual function interact in people with chronic pelvic pain and may inform future educational and clinical approaches.

Detailed description

Chronic pelvic pain (CPP) is defined as persistent or recurrent pelvic pain lasting at least six months and is associated with substantial physical, psychological, and social consequences. Beyond pain intensity, cognitive and emotional factors such as knowledge about pain mechanisms, pain-related beliefs, and coping strategies play an important role in the experience of chronic pain. Sexual function is frequently affected in people with CPP, and this impairment may be influenced not only by nociceptive factors but also by cognitive and affective variables.

The primary objective of this study is to analyze the associations between knowledge about pain, coping strategies, and sexual function in adults with chronic pelvic pain. Secondary objectives include describing these variables in the study population and examining differences according to sex and educational level.

This is an observational, analytical, cross-sectional study. Adult participants (≥18 years) with a clinical diagnosis of chronic pelvic pain will be recruited from hospital outpatient clinics. Exclusion criteria include current pregnancy, recent major pelvic surgery, active pelvic infection or neoplasm, inability to understand Spanish, or cognitive impairment preventing completion of questionnaires.

After providing written informed consent, participants will complete a set of self-administered questionnaires during a single assessment session. Data collected will include sociodemographic variables (age, sex, educational level), pain duration, pain intensity measured by a visual analogue scale, level of knowledge about pain assessed through a brief ad hoc questionnaire developed for this study with content validation, coping strategies assessed using the Pain Catastrophizing Scale (PCS), and sexual function assessed using the Arizona Sexual Experience Scale (ASEX). No intervention or modification of usual clinical care is involved.

Data analysis will include descriptive statistics and appropriate comparative and correlational analyses to explore relationships between knowledge, coping strategies, and sexual function. The study involves minimal risk to participants and guarantees voluntary participation, anonymity, and confidentiality of data. Ethical approval will be obtained from the Research Ethics Committee of the Principality of Asturias prior to study initiation.

Primary outcome measures

  • Pain Knowledge Score [Time frame: Day 1]
Secondary outcome measures (4)
  • Pain Beliefs (Pain Beliefs and Perceptions Inventory - PBPI / Pain Beliefs Questionnaire - PBQ) [Time frame: Day 1]
  • Coping Strategies (Pain Catastrophizing Scale - PCS) [Time frame: Day 1]
  • Sexual Function (Arizona Sexual Experience Scale - ASEX) [Time frame: Day 1]
  • Pain Intensity (Visual Analogue Scale - VAS) [Time frame: Day 1]

Eligibility criteria

Inclusion criteria

  • Adults aged 18 years or older.
  • Clinical diagnosis of chronic pelvic pain lasting at least 6 months.
  • Ability to understand spoken and written Spanish.
  • Willingness to participate and provide written informed consent.

Exclusion criteria

  • Current pregnancy.
  • Major pelvic surgery within the previous 3 months.
  • Active pelvic infection or active neoplastic disease.
  • Cognitive impairment or any condition preventing completion of questionnaires.
  • Inability to understand Spanish.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07487025 · UO-DPC-KCS-2026

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗