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

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

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07487025
Acronym
KCS-CPP
Enrollment
50
Registered
2026-03-23
Start date
2026-03-01
Completion date
2026-04-01
Last updated
2026-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Pain, Chronic Pelvic Pain

Keywords

Chronic pelvic pain, pain knowledge, pain education, coping strategies, pain catastrophizing, sexual function, cross-sectional study, observational study

Brief summary

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.

Interventions

None listed

Sponsors

Maria Blanco Diaz
Lead SponsorOTHER
Hospital Universitario Central de Asturias
CollaboratorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Pain Knowledge ScoreDay 1oping strategies related to pain assessed using the Pain Catastrophizing Scale (PCS), with higher scores indicating greater pain catastrophizing.

Secondary

MeasureTime frameDescription
Pain Beliefs (Pain Beliefs and Perceptions Inventory - PBPI / Pain Beliefs Questionnaire - PBQ)Day 1Pain-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.
Coping Strategies (Pain Catastrophizing Scale - PCS)Day 1Coping strategies related to pain assessed using the Pain Catastrophizing Scale (PCS). Higher scores indicate greater pain catastrophizing.
Sexual Function (Arizona Sexual Experience Scale - ASEX)Day 1Sexual function assessed using the Arizona Sexual Experience Scale (ASEX). Higher scores indicate greater sexual dysfunction.
Pain Intensity (Visual Analogue Scale - VAS)Day 1Self-reported pain intensity measured on a 0-10 visual analogue scale, where 0 indicates no pain and 10 indicates maximum imaginable pain.

Contacts

CONTACTMaría Blanco Diaz, PhD.
blancomaria@uniovi.es+34667681858

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 26, 2026