Clinical Trial: Psychosocial Factors and Central Sensitization in Chronic Pelvic Pain

Study Status: Enrolling by invitation
Recruit Status: Enrolling by invitation
Study Type: Observational

Official Title: Psychosocial Factors and Central Sensitization in Chronic Pelvic Pain

Brief Summary: 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 Summary: 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.
Sponsor: University of Valencia

Current Primary Outcome: Interview on psychosocial factors [ Time Frame: Day 1 ]

Original Primary Outcome: Same as current

Current Secondary Outcome:

  • Survey of Pain Attitudes-35 (SOPA-35) [ Time Frame: Day 1 ]
  • Multidimensional Pain Inventory (MPI) - Interference Scale [ Time Frame: Day 1 ]
  • Oswestry Disability Index [ Time Frame: Day 1 ]
  • Hospital Anxiety and Depression Scale (HADS) [ Time Frame: Day 1 ]
  • Pain Catastrophizing Scale [ Time Frame: Day 1 ]
  • Coping Strategies Questionnaire (CSQ) [ Time Frame: Day 1 ]
  • Tampa Scale for Kinesiophobia (TSK) -11 [ Time Frame: Day 1 ]
  • Neurophysiology of pain questionnaire (NPQ) [ Time Frame: Day 1 ]
  • Female Sexual Function Index (FSFI) [ Time Frame: Day 1 ]
  • Patient Specific Functional Scale (PSFS) [ Time Frame: Day 1 ]
  • Patient Health Questionnaire (PHQ) [ Time Frame: Day 1 ]
  • Quantitative Sensory Testing-Pain Pressure Threshold (PPT) [ Time Frame: Day 2 ]
    in kg/s
  • Quantitative Sensory Testing-Temporal Summation (TS) [ Time Frame: Day 2 ]
    in kg/s
  • Quantitative Sensory Testing-Conditioned Pain Modulation (CPM) [ Time Frame: Day 2 ]
    in kg/s


Original Secondary Outcome: Same as current

Information By: University of Valencia

Dates:
Date Received: July 20, 2016
Date Started: January 2016
Date Completion:
Last Updated: August 1, 2016
Last Verified: August 2016