Educational Program Interventions for Patients Suffering From Persistent Pelvic Pain and Their Effects Over Pain and Functionality. A Multi-centered Randomized Clinical Trial.
Overview
- Phase
- N/A
- Intervention
- Not specified
- Conditions
- Pain
- Sponsor
- University of Valencia
- Enrollment
- 69
- Locations
- 1
- Primary Endpoint
- Visual Analogue Scale
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
Patients suffering pelvic persistent pain deal with significant pain that affects their quality of life. Often, conservative treatment interventions are scarce for these patients and are therefore not considered. Education has been developed as a relevant tool in the treatment of patients who suffer from chronic pain or any other pain processing alterations, and has the potential to become a powerfull treatment alternative.
Detailed Description
In this intervention, the effects of implementing educational programs in patients suffering from pelvic persistent pain will be assessed. Patients with pelvic persistent pain have both problems directly related with their pain and other issues that appear derived from suffering pain over a determined period, such as alterations in the sexuality or overall quality of life. Facing these patients is a challenge for professionals, and many can't find the treatment that properly fits the patient's clinical presentation. Education, and educating patients on their problem, is an exponentially growing alternative used in Physical Therapy involving patients who suffer from a dysfunctional pain, chronic pain, or any kind of pain presentation that affects the patient's well-being. This study will assess firstly if the implementation of a pain-related education program is relevant in the treatment of pelvic persistent pain, and will further observe which modality (presential workshops or online-accessed material) is the most effective involving adherence and improvement.
Investigators
Borja Pérez-Domínguez
Associate Professor
University of Valencia
Eligibility Criteria
Inclusion Criteria
- •Patients over 18 years-old suffering from dyspareunia for more than 3 months
Exclusion Criteria
- •Patients suffering from a previous medical condition that explains logically the presence of pain
Outcomes
Primary Outcomes
Visual Analogue Scale
Time Frame: Baseline to week 4
Pain intensity assessment instrument. Minimum value 0, maximum value 10. Higher scores mean worse outcome
Secondary Outcomes
- Survey of Pain Attitudes(Baseline to week 4)
- Pain Catastrophizing Scale(Baseline to week 4)
- Female Sexual Function Index(Baseline to week 4)