Effects of Pelvic Floor Training in Male Chronic Pelvic Pain, Correlation Between Subjective and Objective Outcomes
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Простыми словами
Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.
- Что изучают
- В протоколе указаны: Pelvic floor re-education using bio-feedback and home training.
- Кому может быть актуально
- Состояния в реестре: Chronic Pelvic Pain Syndrome, Chronic Prostatitis With Chronic Pelvic Pain Syndrome, Chronic Prostatitis, Pelvic Floor; Relaxation. Базовые параметры: от 18 лет · Мужчины.
- Что важно проверить
- Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
- Где проводится
- Швеция
- Следующий шаг
- Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
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Официальное название
Long Term Effects of Pelvic Floor Re-education in Men With Chronic Pelvic Pain, Using Bio-feedback and Home Training - Subjective Outcomes in Correlation to Objective Measurements of the Lower Urinary Tract and Pelvic Floor
Обзор
The goal of this randomized controlled study is to establish the long-term effect of pelvic floor re-education using biofeedback and home training for men with chronic pelvic pain. The main questions it aims to answer are if pelvic floor re-education using bio-feedback and home training will give a long-lasting improvement in symptoms, assessed with a validated symptom score (the National Institute of Health - Chronic Prostatitis Symptom Index) and if an improvement in symptoms can be correlated to objective measurements of pelvic floor function. Participants will be asked to do pelvic floor exercises daily during six months with additional sessions of bio-feedback training. The control group will have no changes in their on-going treatment for their chronic pelvic pain and will be offered to enter the treatment group after six months.
Подробное описание
At baseline all included study subjects will fill in a validated symptom score, the National Institute of Health - Chronic Prostatitis Symptom Index (NIH-CPSI) and have an assessment of their pelvic floor muscles and undergo a urodynamic evaluation.
The intervention group will perform short daily session of pelvic floor muscle training at home during six months in combination with four bio-feedback sessions during the first months. The study subjects will receive an individual instruction based on the pelvic floor assessment from the baseline visit. The study subjects will report their training in a digital diary.
A reevaluation will be done at three, six and twelve months. At six and 12 months repeating the baseline tests. At three months a renewed assessment of muscle function and the NIH-CPSI questionnaire.
The control group will be instructed not to engage in any new treatment for their chronic pelvic pain during the study period. After the six months evaluation all participants in the control group will be offered to be enrolled in the treatment group, with the same set-up and follow-up as the treatment group.
Вмешательства
- Другое Pelvic floor re-education using bio-feedback and home training
Pelvic floor re-education using bio-feedback and home training
Первичные конечные точки
- Change in symptom score on the National Institute of Health-Chronic Prostatitis Symptom Index questionnaire [Срок оценки: Measured 3, 6 and 12 months after inclusion]
Вторичные конечные точки (7)
- Change in sub score on the National Institute of Health-Chronic Prostatitis Symptom Index questionnaire [Срок оценки: Measured 3, 6 and 12 months after inclusion]
- Changes in global voiding function using free flow non-invasive urodynamic testing [Срок оценки: Measured 6 and 12 months after inclusion]
- Changes in global storing function of the bladder using invasive urodynamics, cystometry [Срок оценки: Measured 6 and 12 months after inclusion]
- Changes in global voiding function using invasive urodynamics, pressure-flow study [Срок оценки: Measured 6 and 12 months after inclusion]
- Changes in urethral pressure using invasive urodynamics, urethral pressure profile [Срок оценки: Measured 6 and 12 months after inclusion]
- Changes in pelvic floor muscle assessment according to test specifics by Frawley et al 2021 and the modified Oxford Scale according to Laycock et al 2001. [Срок оценки: Measured 3, 6 and 12 months after inclusion]
- Correlation between subjective and objective measurements [Срок оценки: Measured 3, 6 and 12 months after inclusion]
Критерии участия
Критерии включения
- Men over the age of 18, residents in Sweden, diagnosed with Chronic Primary Pelvic Pain Syndrome (CPPPS) according to the International Statistical Classification of Diseases and Related Health Problems (ICD-10) (N41.1 (chronic prostatitis), N41.9 (Inflammatory disease of prostate, unspecified), N50.8F (Chronic Pelvic Pain Syndrome in men)
Критерии исключения
- Cancer in the abdomen or pelvic organs (current or previous)
- Congenital anomalies affecting the pelvic region (Bladder exstrophy, Myelomeningocele etc.)
- Transsexual male, (i.e. at birth biologically female)
- Diseases affecting the nerve function to the pelvic and/or lower extremities, other disease or ongoing treatment that could have an impact on the outcome of the study.
- Incapability to participate in testing or follow training instructions due to mental incapacity, language difficulties etc.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Простое слепое
- Основная цель
- Лечение
Центры проведения
Швеция · 1 центр
- Karolinska University Hospital — Stockholm
Публикации
- Hallencreutz Grape H, Nordgren B, Renstrom Koskela L. Long-term effects of pelvic floor training in male chronic pelvic pain, correlation between subjective and objective outcomes: a study protocol for a randomised controlled trial. BMJ Open. 2024 Nov 4;14(11):e087620. doi: 10.1136/bmjopen-2024-087620. PMID 39496364
Идентификаторы
NCT: NCT06115083 · K 2023-4671