Physiotherapeutic Approach to Superficial and Deep Dyspareunia in Women With Chronic Pelvic Pain: Comparison Between In-person and Telehealth Care.
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 入组人数
- 72
- 试验地点
- 1
- 主要终点
- Visual Analog Scale (EAV)
研究概览
简要总结
Adequate sexual function is considered an important factor in satisfaction and overall quality of life for both men and women. It is estimated 16% to 40% of women suffer from some form of sexual dysfunction, which is currently considered a public health problem and its investigation is recommended because it causes significant changes in the quality of life of these women. Among the painful disorders, genitopelvic pain, which includes dyspareunia, vaginismus and vulvodynia, dyspareunia stands out, which involves the appearance of pain during or after sexual intercourse, directly affecting physical health, as well as sexual and mental well-being. Among the treatment techniques for dyspareunia in women with chronic pelvic pain, there is the Thiele massage, which provides an inhibitory effect on muscle tension caused by spasms, relaxing, stretching and relieving coital pain. In this sense, we know that physiotherapy treatment has an important role in improving pain symptoms, since musculoskeletal dysfunction may be present in women with dyspareunia, which makes it relevant to verify whether the approach via telecare would have the same effectiveness as the in-person technique that has scientific proof, since through telecare the woman would not be exposed to the risks that are inherent to going to an outpatient clinic, it could cover more women and this would also bring a greater cost-benefit to the unified health system.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Women diagnosed with CPP and deep or shallow penetration dyspareunia;
- •Over 18 years of age;
- •Willingness to voluntarily participate in the study, accepting randomization to either of the two treatment arms;
- •Signature of the Free and Informed Consent Form (FICF).
排除标准
- •Women with penetrative dyspareunia without pelvic floor muscle spasm;
- •Women without an active sex life
研究组 & 干预措施
Face-to-face treatment
Treatment through face-to-face outpatient care
干预措施: Face-to-face treatment (Procedure)
Telecare
Teleservice via video call
干预措施: Telecare (Procedure)
结局指标
主要结局
Visual Analog Scale (EAV)
时间窗: From acceptance to participate in the study until the end in 10 weeks in the reassessment.
The visual analog scale (VAS) for pain is the most widely used unidimensional scale in clinical practice due to its feasibility, speed, and clinical application. It measures pain from 0 to 10, with higher scores indicating greater pain.
次要结局
未报告次要终点
研究者
Hellen Maria Feitoza De Almeida
Principal Investigator
University of Sao Paulo
