跳至主要内容
临床试验/NCT05311267
NCT05311267Unknown不适用

Effects of Action Observation Training (AOT) in the Achievement of Urinary Continence in Men After Robot-assisted Laparoscopic Prostatectomy (RALP)

Istituto Clinico Humanitas1 个研究点 分布在 1 个国家目标入组 92 人开始时间: 2020年10月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
92
试验地点
1
主要终点
Changes in continence using "24 hours pad test"

研究概览

简要总结

Urinary incontinence (UI) is one of the most common side effects of radical prostatectomy (RP) and compromises men's quality of life. The first line treatment for urinary incontinence is the conservative approach of Pelvic Floor Muscle Training (PFMT) but, up to date, there seems to be no statistically significant difference in the effectiveness of several proposed physiotherapy treatments.

Literature highlights the importance of also adding an educational component regarding the intentional contraction of the pelvic floor muscles (a skill termed "the Knack"). Moreover, in some studies, carried out on a sample of women, was introduced the use of virtual reality. This increased the adherence to treatment and showed an improvement in urinary continence. In addition to virtual reality, another intervention methodology used in physiotherapy is the one of Action Observation training (AOT) whose effectiveness has been proven both in sports and rehabilitation.

However, currently the effect of this innovative type of treatment has not yet been studied in men with UI following radical prostatectomy intervention.

The aim of this clinical study is to investigate the effectiveness of using AOT on urinary incontinence in subjects undergoing robotic radical prostatectomy.

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

性别
Male
接受健康志愿者
否

入选标准

  • •Patients who have undergone Robot-assisted Laparoscopic Prostatectomy with post-operative IU.
  • •Objectivity of recruitment and contraction of pelvic floor musculature (PP) at manual perineal testing.

排除标准

  • •Preoperative incontinence
  • •Pre-intervention radiotherapy
  • •Previous urogenital surgery beyond Robot-assisted Laparoscopic Prostatectomy.
  • •Concomitant presence of neurological, internal or musculoskeletal diseases that may affect functional or motor recovery.
  • •Less than 5 seconds of endurance in PP contraction

研究组 & 干预措施

AOT

Experimental

Participants who, in addiction to standard rehabilitation program after surgery (isometric exercises), underwent two training session of action observation therapy.

干预措施: Action observation training (Other)

Control group

No Intervention

Participants who received standard rehabilitation program after surgery. The control group, before performing the functional exercises watched two videos of different landscapes lasting 4 minutes each.

结局指标

主要结局

Changes in continence using "24 hours pad test"

时间窗: Both groups will be evaluated 45 days after surgery (T0), 1-week after T0 (T1), 2 weeks after T0 (T2), 4 weeks after T0 (T4), 6 weeks after T0 (T6) and 8 weeks after T0 (T8), 3 months after T8 (T9).

The primary outcome is to investigate if there is a difference in continence between the experimental and the control group at each physiotherapy session and compared to the baseline (T0).To quantify the extent of these losses, the weight of absorbent devices used by patients in the 24 hours prior to each evaluation will be measured.

次要结局

  • Changes in urinary symptoms using International Prostatic Symptoms Score (IPSS)(Both groups will be evaluated 45 days after surgery (T0), 8 weeks after T0 (T8) or earlier in case of achievement of the primary goal in previous sessions (T1, T2, T4, T6), and 3 months after T8 (T9).)
  • Changes in the quality of life using quality life index (QoL index) 0-6(Both groups will be evaluated 45 days after surgery (T0), 8 weeks after T0 (T8) or earlier in case of achievement of the primary goal in previous sessions (T1, T2, T4, T6), and 3 months after T8 (T9).)
  • Changes in urinary symptoms using International Consultation on Incontinence Questionnaire Short Form (ICIQ-SF)(Both groups will be evaluated 45 days after surgery (T0), 8 weeks after T0 (T8) or earlier in case of achievement of the primary goal in previous sessions (T1, T2, T4, T6), and 3 months after T8 (T9).)

研究者

发起方
Istituto Clinico Humanitas
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验