Psychosocial Factors and Central Sensitization in Chronic Pelvic Pain

NCT ID: NCT02856334

Last Updated: 2016-08-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-01-31

Brief Summary

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The purpose of this study is to determine if the psychosocial factors in women with chronic pelvic pain are predisposing, precipitant or maintenance factors, and relate these factors with central sensitization and dysfunctional pain.

Detailed Description

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This study pretends clarify the psychosocial factors presents in women with chronic pelvic pain, and determine if this factors are predisposing, precipitant or of maintenance, through an interview and a series of validated questionnaires. In addition, these findings will be related to the presence of central sensitization, as measured by quantitative sensory testing.

Conditions

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Pelvic Pain Vulvodynia Pudendal Neuropathy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Study Groups

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Chronic pelvic pain

Women with chronic pelvic pain

No interventions assigned to this group

Control group

Healthy women

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Age between 18 and 55 years
* Chronic pelvic pain diagnosis, defined as persistent pain in pelvis related structures
* Pain duration ≥6 months
* Average pain intensity ≥3/10 in NRS during the previous week
* To understand the objectives of the study

Exclusion Criteria

* Suspicion or knowledge of current organic pathology that requires medical or surgical treatment
* Pain as a consequence of surgery known
* Pending litigation or financial compensation
* Psychiatric disorders: major depression, bipolar syndrome, etc ..
* Cognitive difficulties
* Not sign the informed consent
Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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University of Valencia

OTHER

Sponsor Role lead

Responsible Party

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Rafael Torres Cueco

PT

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Rafael Torres-Cueco

Role: PRINCIPAL_INVESTIGATOR

Locations

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Rafael Torres

Valencia, Valencia, Spain

Site Status

Valencia, Valencia, Spain

Site Status

Countries

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Spain

Other Identifiers

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0117

Identifier Type: -

Identifier Source: org_study_id

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