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NCT Number: NCT07487025

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

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

  1. Pain Knowledge Score

    Time frame: Day 1

    oping strategies related to pain assessed using the Pain Catastrophizing Scale (PCS), with higher scores indicating greater pain catastrophizing.

Secondary outcomes

  1. Pain Beliefs (Pain Beliefs and Perceptions Inventory - PBPI / Pain Beliefs Questionnaire - PBQ)

    Time frame: Day 1

    Pain-related beliefs assessed using the validated Spanish version of the PBPI/PBQ, which evaluates cognitive beliefs about pain such as permanence, mystery, constancy, and self-blame. Higher scores indicate stronger endorsement of maladaptive pain beliefs.

  2. Coping Strategies (Pain Catastrophizing Scale - PCS)

    Time frame: Day 1

    Coping strategies related to pain assessed using the Pain Catastrophizing Scale (PCS). Higher scores indicate greater pain catastrophizing.

  3. Sexual Function (Arizona Sexual Experience Scale - ASEX)

    Time frame: Day 1

    Sexual function assessed using the Arizona Sexual Experience Scale (ASEX). Higher scores indicate greater sexual dysfunction.

  4. Pain Intensity (Visual Analogue Scale - VAS)

    Time frame: Day 1

    Self-reported pain intensity measured on a 0-10 visual analogue scale, where 0 indicates no pain and 10 indicates maximum imaginable pain.

Study contacts

Contact information is provided by the study sponsor or research team.

María Blanco Diaz, PhD.

CONTACT

[email protected]

+34667681858

Sponsors and collaborators

Lead sponsor

Maria Blanco Diaz

Other

Collaborators

  • Hospital Universitario Central de Asturias

Registry information

Official study title

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

Acronym: KCS-CPP

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Mar 23, 2026
Registry last updated
Mar 25, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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