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Clinical Trials/NCT01994343
NCT01994343
Unknown
N/A

Musculoskeletal Disturbances in Women With Chronic Pelvic Pain

Universidad de Granada1 site in 1 country38 target enrollmentNovember 2013
ConditionsChronic Pain

Overview

Phase
N/A
Intervention
Not specified
Conditions
Chronic Pain
Sponsor
Universidad de Granada
Enrollment
38
Locations
1
Primary Endpoint
Change in postural control
Last Updated
7 years ago

Overview

Brief Summary

Chronic pelvis pain is very common between adult women. Significant progress is made in clarifying the multifactorial model of chronic pain pathogenesis, but a more complete assessment is important in order to improve the therapeutic approach. The purpose of this study is stablish a clinical and symptomatological profile of women with chronic pelvic pain.

Detailed Description

Chronic pelvic pain is defined as non-menstrual or noncyclic pelvic pain with duration of at least 6 months. This pain interfere with habitual activities and requires clinical or surgical treatment. It is a complex interaction between the gastrointestinal, urinary, gynecologic, musculoskeletal, neurologic and endocrine systems influenced by psychological factors. Its prevalence range between 3 and 8% among women aged 15-73 years, ranging from 14 to 24% among women of reproductive age. It is very important a multidimensional approach in order to stablish a more specific profile.

Registry
clinicaltrials.gov
Start Date
November 2013
End Date
August 2018
Last Updated
7 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Marie Carmen Valenza

assistant professor

Universidad de Granada

Eligibility Criteria

Inclusion Criteria

  • Clinical diagnosis of chronic pelvic pain.
  • More than eighteen years.
  • Non-menstrual or noncyclic pelvic pain.
  • Duration of pain of at least 6 months.

Exclusion Criteria

  • Duration of pain less than 6 months.
  • Women who were pregnant in the last 12 months

Outcomes

Primary Outcomes

Change in postural control

Time Frame: Change from baseline postural control at 8 weeks

Postural control will be assessed using the Mini-BESTest, a 14-item test that focuses on dynamic balance, specifically anticipatory transitions (six items), reactive postural control (six items), sensory orientation (six items), and dynamic gait (10 items). Each item is scored from 0 to 2; a score of 0 indicates that a person is unable to perform the task, whereas a score of 2 is normal. The best score is the maximum amount of points, being 28.

Secondary Outcomes

  • Self perceived health status(Baseline, 8 weeks.)
  • Trigger points evaluation(baseline)
  • Spinal assessment(baseline)
  • Nervous assessment(baseline)
  • Balance under dual task conditions(Baseline, 8 weeks)

Study Sites (1)

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